Patent Application
20230140293
The instant application contains a Sequence Listing of SEQ ID NOS 1-396 which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety and forms part of the specification. Said ASCII copy, created on May 25, 2018, is named 1234300_00295WO1_SL.txt and is 1,243,033 bytes in size. Additional sequences included in the Specification and Drawings and will be furnished in ASCII form in accordance with the sequence listing requirements.
The present invention relates in general, to a composition suitable for use in inducing anti-HIV-1 antibodies, and, in particular, to immunogenic compositions comprising envelope proteins and nucleic acids to induce cross-reactive neutralizing antibodies and increase their breadth of coverage. The invention also relates to methods of inducing such broadly neutralizing anti-HIV-1 antibodies using such compositions.
The development of a safe and effective HIV-1 vaccine is one of the highest priorities of the scientific community working on the HIV-1 epidemic. While anti-retroviral treatment (ART) has dramatically prolonged the lives of HIV-1 infected patients, ART is not routinely available in developing countries.
The ability to stimulate germline B cells that give rise to broadly neutralizing antibodies (bNAbs) is a major goal for HIV-1 vaccines. BNAbs that target the CD4-binding site (CD4bs) of HIV-1 and exhibit extraordinary potency and breadth of neutralization are particularly attractive to elicit with vaccines. Glycans that border the CD4bs and impede the binding of germline-reverted forms of CD4bs bNAbs are potential barriers to naïve B cell receptor engagement. In some aspects, pseudovirus neutralization was used as a means to identify Env modifications that permit native Env trimer binding to germline reverted CD4bs bNAb CH235.12 (VH1-46) as a surrogate for naïve B cell receptor engagement.
Site-directed mutagenesis was used to create strategic mutants of autologous CH0505TF Env. The mutants were produced in cells lacking the enzyme N-acetylglucosaminyltransferase (GnTI-) to enrich for Man5 glycoforms of N-linked glycans that would otherwise be fully processed into complex-type glycans. Naturally-glycosylated and Man5-enriched forms of parental and mutant Envs were tested for neutralization by the CH235 antibody lineage that included the unmutated common ancestor (UCA), intermediates and mature forms of CH235.12. Corresponding SOSIP.664 trimers were tested for UCA binding. These strategies are used to create germline-targeting and reverse-engineered immunogens to Elicit CH235.12 Lineage BNAbs.
In one aspect the invention provides that Man5-enriched CH0505TF containing two VRC01-class resistance mutations, N279K (loop D) and G458Y (V5 region), was highly susceptible to neutralization by CH235 UCA. This double mutant was also neutralized by the UCA when produced in 293T cells but was 100× more sensitive when produced in GnTI-cells (Man5-enrichment). Neutralization predicted nM affinity binding to various envelopes, e.g. but not limited to mutated, Man5-enriched CH0505TF SOSIP.664 trimers.
In one aspect the invention provides recombinant HIV-1 envelope polypeptides from Tables 1A-B, Examples 2-13, or any other envelope, wherein the envelope comprises G458Mut. In some embodiments, optionally the polypeptide is enriched for Man5 glycoforms of N-linked glycans. In certain embodiments G458Mut is G458Y. In certain embodiments non-limiting embodiments of G458Mut are described in Ex. 10 and
In one aspect, the invention provides a recombinant HIV-1 envelope polypeptide from Tables 1A-B, Examples 2-13, or any other envelope, wherein the polypeptide is enriched for Man5 glycoforms of N-linked glycans, and wherein in some embodiments the polypeptide has differential binding and/neutralization compared to fully glycosylated envelope.
In one aspect the invention provides a nucleic acid encoding the recombinant polypeptides of the invention.
In one aspect the invention provides a recombinant trimer comprising three identical protomers of an HIV-1 envelope polypeptide of the invention. In one aspects the invention provides an immunogenic composition comprising the recombinant trimer of the invention and a carrier, wherein the trimer comprises three identical protomers of an HIV-1 envelope polypeptide. In certain embodiments, the composition comprises which are substantially homogenous.
In one aspect the invention provides an immunogenic composition comprising nucleic acid encoding the recombinant HIV-1 envelope polypeptide of the invention and a carrier.
In certain embodiments, the recombinant HIV-1 envelope polypeptide is HIV-1 CH505 M5. In certain embodiments, the recombinant HIV-1 envelope polypeptide is HIV-1 CH505 T/F. In certain embodiments, the recombinant HIV-1 envelope polypeptide is HIV-1 CH505 M11.
In one aspect the invention provides methods of using the immunogens of the invention to induce immune response, wherein in some embodiments without limitation these immune responses stimulate germline B cells that give rise to broadly neutralizing antibodies (bNAbs). Non-limiting embodiments of methods are described in
Any one of the methods of the invention wherein the administration step can alternatively, or in addition, comprise administering a nucleic acid encoding the corresponding HIV-1 polypeptide(s) in an amount sufficient to induce an immune response.
Any one of the methods of the invention wherein the method comprises administering a composition comprising HIV-1 envelope CH505 M5 G458Mut or a nucleic acid encoding HIV-1 envelope CH505 M5 G458Mut.
Any one of the methods of the invention further comprising administering a composition comprising HIV-1 envelope CH505 M5, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans.
Any one of the methods of the invention further comprising administering a composition comprising HIV-1 envelope CH505 M5 G458Mut, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans wherein the envelope is enriched for Man5 glycoforms of N-linked glycans.
Any one of the methods of the invention wherein the method comprises administering a composition comprising HIV-1 envelope CH505 M5 G458Mut, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans.
Any one of the methods of the invention further comprising administering a composition comprising CH505 M5, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans
Any one of the methods of the invention further comprises administering a composition comprising HIV-1 envelope CH505 M5 G458Mut or a nucleic acid encoding HIV-1 envelope CH505 M5 G458Mut.
Any one of the methods of the invention further comprising administering a composition comprising HIV-1 envelope CH505 T/F, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans.
Any one of the methods of the invention further comprising administering a composition comprising HIV-1 envelope CH505 M5, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans and HIV-1 envelope CH505 M5 G458Mut, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans.
Any one of the methods of the invention further comprising administering a composition comprising HIV-1 envelope CH505 M5 and HIV-1 envelope CH505 M5 G458Mut.
Any one of the methods of the invention further comprising administering a composition comprising HIV-1 envelope CH505 T/F, wherein the envelope is enriched for Man5 glycoforms of N-linked glycans.
Any one of the methods of the invention further comprising administering a composition comprising HIV-1 envelope CH 505 T/F.
Any one of the methods of the invention wherein the polypeptide is gp120 envelope, gp120D8 envelope, a gp140 envelope (gp140C, gp140CF, gp140CFI) as soluble or stabilized protomer of a SOSIP trimer, a gp145 envelope, a gp150 envelope, or a transmembrane bound envelope.
Any one of the methods or compositions of the invention wherein the composition further comprises an adjuvant.
Any one of the methods of the invention further comprising administering an agent which modulates host immune tolerance.
Any one of the methods or compositions of the invention wherein the polypeptide administered is multimerized. Non-limiting embodiments of multimerized envelopes include ferritin particles, liposomes, nanoparticles, or any other suitable form.
Any one of the methods of the invention further comprising administering an additional immunogen. Non-limiting embodiments are described Example 2-13.
In some aspects, these findings advance our understanding of the restrictions imposed by glycans in the elicitation of CD4bs bNAbs and provide a conceptual framework and methods for immunogen design to initiate and mature the CH235.12 bNAb lineage.
In one aspect, the invention is directed to immunogens and methods for germline B cell stimulation and maturation by reverse engineering of HIV-1 envelopes. B cell stimulation is a key initial step in the ability of HIV vaccines to elicit broadly neutralizing antibodies (bNAbs). In some aspects the invention provides modifications of HIV-1 envelopes to trigger germline activation and drive subsequent B cell maturation of bNAbs, including but not limited to CD4bs bNAbs.
In certain aspects, the invention is directed to a recombinant HIV-1 envelope polypeptide, including but not limited to an envelope from Tables 1A-B, wherein the envelope comprises G458Mut and/or glycosylation pattern similar to the glycosylation patter of an envelope grown in GnTI−/− cells. In certain embodiments, the polypeptide is a non-naturally occurring protomer designed to form an envelope trimer. The glycosylation pattern of GnTI−/− grown recombinant polypetides is well known. In some embodiments, when produced in GnTI−/− cells the polypeptides are enriched for Man5 glycoforms of N-linked glycans.
In certain aspects, the invention provides nucleic acids encoding these recombinant polypeptides. In certain aspects, the invention provides recombinant cells and/or population of recombinant cells comprising nucleic acids encoding the recombinant polypeptides of the invention.
In certain embodiments, the invention provides a recombinant trimer comprising three identical protomers of an envelope from Tables 1A-B. In certain embodiments, the invention provides an immunogenic composition comprising the recombinant trimer and a carrier, wherein the trimer comprises three identical protomers of an HIV-1 envelope listed in Tables 1A-B.
In certain embodiments, the invention provides an immunogenic composition comprising nucleic acid encoding a recombinant HIV-1 envelope and a carrier. The compositions could comprise an adjuvant.
In certain embodiments the recombinant envelope is HIV-1 envelope CH505 M5 or a nucleic acid encoding HIV-1 envelope CH505M5, wherein the HIV-1 CH505 M5 envelope comprises a G458Mut and is recombinantly produced in 293T cells so that glycosylation pattern is not Man5 enriched. In certain embodiments the recombinant envelope is HIV-1 envelope CH505 M5 or a nucleic acid encoding HIV-1 envelope CH505 M5, wherein the HIV-1 CH505 M5 envelope does not comprise a G458Mut and is recombinantly produced in GnTI−/− cells so that glycosylation pattern is Man5 enriched. In certain embodiments the recombinant envelope is HIV-1 envelope CH505 M5 or a nucleic acid encoding HIV-1 envelope CH505 M5, wherein the HIV-1 CH505 M5 envelope comprises a G458Mut and is recombinantly produced in GnTI−/− cells so that glycosylation pattern is Man5 enriched.
In certain embodiments the recombinant envelope is HIV-1 envelope CH505 M11 or a nucleic acid encoding HIV-1 envelope CH505 M11, wherein the HIV-1 CH505 M11 envelope comprises a G458Mut and is recombinantly produced in 293T cells so that glycosylation pattern is not Man5 enriched. In certain embodiments the recombinant envelope is HIV-1 envelope CH505 M11 or a nucleic acid encoding HIV-1 envelope CH505 M11, wherein the HIV-1 M11 envelope does not comprise a G458Mut and is recombinantly produced in GnTI−/− cells so that glycosylation pattern is Man5 enriched. In certain embodiments the recombinant envelope is HIV-1 envelope CH505 M11 or a nucleic acid encoding HIV-1 envelope CH505 M11, wherein the HIV-1 CH505 M11 envelope comprises a G458Mut and is recombinantly produced in GnTI−/− cells so that glycosylation pattern is Man5 enriched.
In certain embodiments the recombinant envelope is HIV-1 envelope CH505 T/F or a nucleic acid encoding HIV-1 envelope CH505 T/F, wherein the HIV-1 CH505 T/F envelope comprises a G458Mut and is recombinantly produced in 293T cells so that glycosylation pattern is not Man5 enriched. In certain embodiments the recombinant envelope is HIV-1 envelope CH505 T/F or a nucleic acid encoding HIV-1 envelope CH505 T/F, wherein the HIV-1 CH505 T/F envelope does not comprise a G458Mut and is recombinantly produced in GnTI−/− cells so that glycosylation pattern is Man5 enriched. In certain embodiments the recombinant envelope is HIV-1 envelope CH505 T/F or a nucleic acid encoding HIV-1 envelope v, wherein the HIV-1 CH505 T/F 5 envelope comprises a G458Mut and is recombinantly produced in GnTI−/− cells so that glycosylation pattern is Man5 enriched.
In certain aspects the invention provides methods of inducing immune responses using the inventive immunoges. In one embodiment the invention provides a method of inducing an immune response in a subject comprising administering a composition in an amount sufficient to induce an immune response, wherein the composition comprises any suitable form of a nucleic acid(s) encoding an HIV-1 envelope(s) from one or more of the following groups:
In certain embodiments the methods comprise administering immunogens with increasing BCR stimulation (See e.g.
In some embodiments the methods further comprise administering HIV-1 envelope w20.14 or a nucleic acid encoding HIV-1 envelope w20.14, followed by administering HIV-1 envelope w30.20 or a nucleic acid encoding HIV-1 envelope w30.20, and followed by administering HIV-1 envelope w30.12 or a nucleic acid encoding HIV-1 envelope w30.12.
In some embodiments the methods further comprise administering HIV-1 envelope w136.B18 or a nucleic acid encoding HIV-1 envelope w136.B18.
In some embodiments the methods further comprise administering HIV-1 envelope w30.25 or a nucleic acid encoding HIV-1 envelope w30.25, HIV-1 envelope w53.25 or a nucleic acid encoding HIV-1 envelope w53.25, HIV-1 envelope w53.29 or a nucleic acid encoding HIV-1 envelope w53.29.
A method of inducing an immune response in a subject comprising administering a composition in an amount sufficient to induce an immune response, wherein the composition comprises any suitable form of a nucleic acid(s) encoding an HIV-1 envelope(s) in an amount sufficient to induce an immune response from one or more of the following groups:
In certain embodiments, the invention provides compositions and method for induction of immune response, for example cross-reactive (broadly) neutralizing Ab induction. In certain embodiments, the methods use compositions comprising “swarms” of sequentially evolved envelope viruses that occur in the setting of bnAb generation in vivo in HIV-1 infection.
In certain aspects the invention provides modified HIV envelopes, wherein the modified envelopes are suitable for use as immunogens for germline targeting of CD4bs broadly neutralizing antibodies. In certain aspects, the modified envelopes of the invention could be used in assays to determine whether CD4bs broad neutralization antibodies lineage(s) have been induced by vaccine regimens.
In certain aspects the invention provides compositions comprising a selection of HIV-1 envelopes and/ or nucleic acids encoding these envelopes as described herein for example but not limited to Selections as described herein. Without limitations, these selected combinations comprise envelopes which provide representation of the sequence (genetic) and antigenic diversity of the HIV-1 envelope variants which lead to the induction and maturation of the CH103 and CH235 antibody lineages. In certain embodiments the selections of envelopes comprise envelopes which show differential binding to an antibody or antibodies from CH103 and CH235 lineages (
In certain embodiments the selections of envelopes comprise envelopes which show differential binding to an antibody or antibodies from CH103 and CH235 lineages (
In certain aspects, the invention provides a kit comprising Env M5, M11, 20.14, 30.20, 30.12, 30.21 30.23, 30.25, 30.28, 53.25, 53.29, 53.31, 78.15, 100.B6 and/or 136.B18. In some embodiments the kit comprises instructions on how to carry out the immunization regimen, including which immunogen(s) are a prime immunization and which immunogen(s) comprise a boost immunization. In some embodiments the kit comprises instructions on administration of the immunogen as a prime or as a boost as part of a prime/boost immunization regimen.
In some embodiments, the kit comprises Env M5, M11, w20.14, w30.20 and/or w136.B18 and instructions on administration of the immunogen as a prime or boost as part of a prime/boost immunization regimen with M5, M11, w20.14, w30.20 and/or w136.B18, including which immunogen(s) are a prime immunization and which immunogen(s) comprise a boost immunization In some embodiments, the kit comprises Env M5, w30.25, w53.25 and/or w53.29 and instructions on administration of the immunogen as a prime or boost as part of a prime/boost immunization regimen with M5, w30.25, w53.25 and/or w53.29, including which immunogen(s) are a prime immunization and which immunogen(s) comprise a boost immunization.
In one aspect the invention provides selections of envelopes from individual CH505, which selections can be used in compositions for immunizations to induce lineages of broad neutralizing antibodies. In certain embodiments, there is some variance in the immunization regimen; in some embodiments, the selection of HIV-1 envelopes may be grouped in various combinations of primes and boosts, either as nucleic acids, proteins, or combinations thereof. In certain embodiments the compositions are pharmaceutical compositions which are immunogenic. In certain embodiments, the compositions comprise amounts of envelopes which are therapeutic and/or immunogenic.
In one aspect the invention provides a composition for a prime boost immunization regimen comprising any one of the envelopes described herein, or any combination thereof wherein the envelope is a prime or boost immunogen. In certain embodiments the composition for a prime boost immunization regimen comprises one or more envelopes from
In one aspect the invention provides a composition comprising any one of the envelopes described herein, or any combination thereof—for example but not limited to selections in Examples and
In some embodiments, CH505 M11 Env is administered first as a prime, followed by a mixture of a next group of Envs. In some embodiments, grouping of the envelopes is based on their binding affinity for the antibodies expected to be induced. In some embodiments, grouping of the envelopes is based on chronological evolution of envelope viruses that occurs in the setting of bnAb generation in vivo in HIV-1 infection. In some embodiments Loop D mutants could be included in either prime and/or boost. In some embodiments, the composition comprises an adjuvant. In some embodiments, the composition and methods comprise use of agents for transient modulation of the host immune response.
In one aspect the invention provides a composition comprising nucleic acids encoding HIV-1 envelope which is a loop D mutant, e.g. M11 or any other suitable D loop mutant or combination thereof, e.g. M11 and M5.
In another aspect the invention provides a method of inducing an immune response in a subject comprising administering a composition comprising HIV-1 envelope M11 and/or M5 as a prime in an amount sufficient to induce an immune response, wherein the envelope is administered as a polypeptide or a nucleic acid encoding the same. A method of inducing an immune response in a subject comprising administering a composition comprising HIV-1 envelope M11 and M5 as a prime in an amount sufficient to induce an immune response, wherein the envelope is administered as a polypeptide or a nucleic acid encoding the same.
In certain embodiments the methods comprise administering any of the selection listed in Example 3. In certain embodiments the methods comprise administering Envs M5, M11, 20.14, 30.28, 30.23, and/or 136.B18. In certain embodiments the methods comprise administering Envs M5, M11, 20.14, 30.20, 30.23, and/or 136.B18. In certain embodiments the methods comprise administering Envs M5, M11, 20.14, 30.20, 30.12, and/or 136.B18. In certain embodiments the methods comprise administering envelopes M5, 30.25, 53.25, and/or 53.29.
In certain embodiments the methods further comprise administering a composition comprising any one of HIV-1 envelope M11, w020.14, w030.28, w078.15, w053.31 or any combination thereof as a boost, wherein the envelope is administered as a polypeptide or a nucleic acid encoding the same.
In certain embodiments the methods comprise administering a composition comprising any one of HIV-1 envelope M11, M5, w020.14, w030.28, w078.15, w053.31 or any combination thereof as a boost, wherein the envelope is administered as a polypeptide or a nucleic acid encoding the same.
In another aspect the invention provides a method of inducing an immune response in a subject comprising administering a composition comprising HIV-1 envelope M11, M5, w020.14, w030.28, w078.15, w053.16, w030.21, w078.33, w100.B6, w053.31 or any combination thereof as a prime and/or boost in an amount sufficient to induce an immune response, wherein the envelope is administered as a polypeptide or a nucleic acid encoding the same.
In certain embodiments, the compositions contemplate nucleic acid, as DNA and/or RNA, or proteins immunogens either alone or in any combination. In certain embodiments, the methods contemplate genetic, as DNA and/or RNA, immunization either alone or in combination with envelope protein(s).
In certain embodiments the nucleic acid encoding an envelope is operably linked to a promoter inserted an expression vector. In certain aspects the compositions comprise a suitable carrier. In certain aspects the compositions comprise a suitable adjuvant.
In certain embodiments the induced immune response includes induction of antibodies, including but not limited to autologous and/or cross-reactive (broadly) neutralizing antibodies against HIV-1 envelope. Various assays that analyze whether an immunogenic composition induces an immune response, and the type of antibodies induced are known in the art and are also described herein.
In certain aspects the invention provides an expression vector comprising any of the nucleic acid sequences of the invention, wherein the nucleic acid is operably linked to a promoter. In certain aspects the invention provides an expression vector comprising a nucleic acid sequence encoding any of the polypeptides of the invention, wherein the nucleic acid is operably linked to a promoter. In certain embodiments, the nucleic acids are codon optimized for expression in a mammalian cell, in vivo or in vitro. In certain aspects the invention provides nucleic acids comprising any one of the nucleic acid sequences of invention. In certain aspects the invention provides nucleic acids consisting essentially of any one of the nucleic acid sequences of invention. In certain aspects the invention provides nucleic acids consisting of any one of the nucleic acid sequences of invention. In certain embodiments the nucleic acid of the invention, is operably linked to a promoter and is inserted in an expression vector. In certain aspects the invention provides an immunogenic composition comprising the expression vector.
In certain aspects the invention provides a composition comprising at least one of the nucleic acid sequences of the invention. In certain aspects the invention provides a composition comprising any one of the nucleic acid sequences of invention. In certain aspects the invention provides a composition comprising at least one nucleic acid sequence encoding any one of the polypeptides of the invention.
In certain aspects the invention provides a composition comprising at least one nucleic acid encoding HIV-1 envelope M11, M5, w020.14, w030.28, w078.15, w053.16, w030.21, w078.33, w100.B6, w053.31 or any combination thereof. Non-limiting examples of combinations are shown in Example 2.
In certain embodiments, the compositions and methods employ an HIV-1 envelope as polypeptide instead of a nucleic acid sequence encoding the HIV-1 envelope. In certain embodiments, the compositions and methods employ an HIV-1 envelope as polypeptide, a nucleic acid sequence encoding the HIV-1 envelope, or a combination thereof.
The envelope used in the compositions and methods of the invention can be a gp160, gp150, gp145, gp140, gp120, gp41, N-terminal deletion variants as described herein, cleavage resistant variants as described herein, or codon optimized sequences thereof. In certain embodiments the composition comprises envelopes as trimers. In certain embodiments, envelope proteins are multimerized, for example trimers are attached to a particle such that multiple copies of the trimer are attached and the multimerized envelope is prepared and formulated for immunization in a human. In certain embodiments, the compositions comprise envelopes, including but not limited to trimers as particulate, high-density array on liposomes or other particles, for example but not limited to nanoparticles. In some embodiments, the trimers are in a well ordered, near native like or closed conformation. In some embodiments the trimer compositions comprise a homogenous mix of native like trimers. In some embodiments the trimer compositions comprise at least 85%, 90%, 95% native like trimers.
The polypeptide contemplated by the invention can be a polypeptide comprising any one of the polypeptides described herein. The polypeptide contemplated by the invention can be a polypeptide consisting essentially of any one of the polypeptides described herein. The polypeptide contemplated by the invention can be a polypeptide consisting of any one of the polypeptides described herein. In certain embodiments, the polypeptide is recombinantly produced. In certain embodiments, the polypeptides and nucleic acids of the invention are suitable for use as an immunogen, for example to be administered in a human subject.
In certain embodiments the envelope is any of the forms of HIV-1 envelope. In certain embodiments the envelope is gp120, gp140, gp145 (i.e. with a transmembrane), gp150. In certain embodiments, gp140 designed to form a stable trimer (See Tables 1A-B,
In certain embodiments, the envelope is in a liposome. In certain embodiments the envelope comprises a transmembrane domain with a cytoplasmic tail embedded in a liposome. In certain embodiments, the nucleic acid comprises a nucleic acid sequence which encodes a gp120, gp140, gp145, gp150, gp160.
In certain embodiments, where the nucleic acids are operably linked to a promoter and inserted in a vector, the vectors is any suitable vector. Non-limiting examples, include, VSV, replicating rAdenovirus type 4, MVA, Chimp adenovirus vectors, pox vectors, and the like. In certain embodiments, the nucleic acids are administered in NanoTaxi block polymer nanospheres. In certain embodiments, the composition and methods comprise an adjuvant. Non-limiting examples include, AS01 B, AS01 E, gla/SE, alum, Poly I poly C (poly IC), polylC/long chain (LC) TLR agonists, TLR7/8 and 9 agonists, or a combination of TLR7/8 and TLR9 agonists (see Moody et al. (2014) J. Virol. March 2014 vol. 88 no. 6 3329-3339) , or any other adjuvant. Non-limiting examples of TLR7/8 agonist include TLR7/8 ligands, Gardiquimod, Imiquimod and R848 (resiquimod). A non-limiting embodiment of a combination of TLR7/8 and TLR9 agonist comprises R848 and oCpG in STS (see Moody et al. (2014) J. Virol. March 2014 vol. 88 no. 6 3329-3339).
In certain aspects the invention provides a cell comprising a nucleic acid encoding any one of the envelopes of the invention suitable for recombinant expression. In certain aspects, the invention provides a clonally derived population of cells encoding any one of the envelopes of the invention suitable for recombinant expression. In certain aspects, the invention provides a sable pool of cells encoding any one of the envelopes of the invention suitable for recombinant expression.
In certain aspects, the invention provides a recombinant HIV-1 envelope polypeptide from Tables 1A-B, wherein the polypeptide is a non-naturally occurring protomer designed to form an envelope trimer. The invention also provides nucleic acids encoding these recombinant polypeptides. Non-limiting examples of amino acids and nucleic acid of such protomers are shown in
In certain aspects the invention provides a recombinant trimer comprising three identical protomers of an envelope from Tables 1A-B. In certain aspects the invention provides an immunogenic composition comprising the recombinant trimer and a carrier, wherein the trimer comprises three identical protomers of an HIV-1 envelope listed in Tables 1A-B. In certain aspects the invention provides an immunogenic composition comprising nucleic acid encoding these recombinant HIV-1 envelopes and a carrier.
In certain aspects the invention provides a selection of HIV-1 envelopes or any suitable form of a nucleic acid encoding HIV-1 envelope for use in an immunization regimen, wherein the selections of envelopes comprises envelopes M5, M11, w20.14, w30.20, w30.12, and w136.B18 (Selection F, e.g. listed in
In certain aspects the invention provides a selection of nucleic acids encoding HIV-1 envelopes for immunization wherein the nucleic acid encodes a gp120 envelope, gp120D8 envelope, a gp140 envelope (gp140C, gp140CF, gp140CFI) as soluble or stabilized protomer of a SOSIP trimer, a gp145 envelope, a gp150 envelope, or a transmembrane bound envelope.
In certain aspects the invention provides a selection of HIV-1 envelopes for immunization wherein the HIV-1 envelope is a gp120 envelope or a gp120D8 variant. In certain embodiments a composition for immunization comprises protomers that form stabilized trimers, e.g. but not limited to SOSIP.III trimers.
In certain embodiments, the compositions for use in immunization further comprise an adjuvant.
In certain embodiments, wherein the compositions comprise a nucleic acid, the nucleic acid is operably linked to a promoter, and could be inserted in an expression vector.
In certain aspects, the invention provides a kit comprising a combination/selection of immunogens of from Tables 1A-B, wherein the polypeptide is a non-naturally occurring protomer designed to form an envelope trimer. In certain aspects, the invention provides a kit comprising a combination/selection of immunogens of from
In one aspect the invention provides a composition for a prime boost immunization regimen comprising one or more envelopes from Tables 1A-B, wherein the polypeptide is a non-naturally occurring protomer designed to form an envelope trimer, wherein the envelope is a prime or boost immunogen. In one aspect the invention provides a composition for a prime boost immunization regimen comprising one or more envelopes from
In certain aspects the invention provides methods of inducing an immune response in a subject comprising administering a composition comprising any suitable form of a nucleic acid(s) encoding an HIV-1 envelope(s) in an amount sufficient to induce an immune response from one or more of the following groups: (a) the selection of envelopes M5, M11, w20.14, w30.20, w30.12, and w136.B18 (Selection F, e.g. listed in
In certain embodiments, the methods further comprise administering HIV-1 envelope w30.25 or a nucleic acid encoding HIV-1 envelope w30.25, HIV-1 envelope w53.25 or a nucleic acid encoding HIV-1 envelope w53.25, HIV-1 envelope w53.29 or a nucleic acid encoding HIV-1 envelope w53.29.
In certain embodiments, the nucleic acid encodes a gp120 envelope, gp120D8 envelope, a gp140 envelope (gp140C, gp140CF, gp140CFI) as soluble or stabilized protomer of a SOSIP trimer, a gp145 envelope, a gp150 envelope, or a transmembrane bound envelope. In certain embodiments, the polypeptide is gp120 envelope, gp120D8 envelope, a gp140 envelope (gp140C, gp140CF, gp140CFI) as soluble or stabilized protomer of a SOSIP trimer, a gp145 envelope, a gp150 envelope, or a transmembrane bound envelope.
In certain aspects, the invention provides a method of inducing an immune response in a subject comprising administering a composition comprising envelope CH505 T/F, followed by envelope w53.16, followed by envelope w78.33 and followed by envelope w100.B6, wherein each composition comprises the envelope as a trimer. In certain embodiments of the method the selection of immunogens is administered as nucleic acids.
In certain embodiments, the methods comprise administering an adjuvant. In certain embodiments, the methods comprise administering an agent which modulates host immune tolerance. In certain embodiments, the administered polypeptide is multimerized in a liposome or nanoparticle. In certain embodiments, the methods comprise administering one or more additional HIV-1 immunogens to induce a T cell response. Non-limiting examples include gag, nef, pol, etc.
In certain aspects, the invention provides a recombinant HIV-1 Env ectodomain trimer, comprising three gp120-gp41 protomers comprising a gp120 polypeptide and a gp41 ectodomain, wherein each protomer is the same and each protomer comprises portions from envelope BG505 HIV-1 strain and gp120 polypeptide portions from a CH505 HIV-1 strain and stabilizing mutations A316W and E64K, (see e.g.
In certain aspects, the invention provides a pharmaceutical composition comprising any one of the recombinant trimers of the invention. In certain embodiments the compositions comprising trimers are immunogenic. The percent trimer in such immunogenic compositions could vary. In some embodiments the composition comprises 70%, 71%, 72%, 73%, 74%,75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% stabilized trimer.
In certain aspects the invention provides any suitable form of a nucleic acid encoding a HIV-1 envelope from the selections of envelopes listed in
To conform to the requirements for PCT patent applications, many of the figures presented herein are black and white representations of images originally created in color.
This approach has been employed to multiple CH505 Env sequences in order to make sequential vaccination regimens. A 4-valent vaccination regimen of SOSIP.II was made. The same 4—valent vaccine was made using the SOSIP.III design. A 6-valent vaccine can be made. Trimers to were analyzed for glycosylation and disulfide bond analysis and the Envs have the expected glycosylation and lack aberrant disulfide bonds.
The development of a safe, highly efficacious prophylactic HIV-1 vaccine is of paramount importance for the control and prevention of HIV-1 infection. A major goal of HIV-1 vaccine development is the induction of broadly neutralizing antibodies (bnAbs) (Immunol. Rev. 254: 225-244, 2013). BnAbs are protective in rhesus macaques against SHIV challenge, but as yet, are not induced by current vaccines.
The ability to stimulate germline B cells that give rise to broadly neutralizing antibodies (bNAbs) is a major goal for HIV-1 vaccine development. bNAbs that target the CD4-binding site (CD4bs) and exhibit extraordinary potency and breadth of neutralization are particularly attractive to elicit with vaccines. Glycans that border the CD4bs and impede the binding of germline-reverted forms of CD4bs bNAbs are potential barriers to naïve B-cell receptor engagement. In some aspects, pseudovirus neutralization was used as a means to identify Env modifications that permit native Env trimer binding to germline reverted CD4bs bNAb CH235.12 (VH1-46). Two mutations (N279K.G458Y), when combined with Man5-enrichment of N-linked glycans that are otherwise processed into complex glycans, rendered autologous CH0505TF Env highly sensitive to neutralization by CH235.12 UCA. These findings suggest a vaccine strategy to initiate and mature the CH235.12 lineage.
In some embodiments, site-directed mutagenesis was used to create mutants of autologous CH0505TF Env. Mutants were produced in 293T/17 and 293S/GnTI-cells lacking the enzyme N-acetylglucosaminyltransferase (GnTI-) to enrich for Man5 glycoforms. Naturally-glycosylated and Man5-enriched forms of parental and mutant Envs were tested for neutralization by the unmutated common ancestor (UCA), intermediates, and mature forms of CH235.12. Various trimers comprising these mutations were tested for UCA binding.
In some aspects, the paradigm of B cell lineage immunogen design (Nature Biotech. 30: 423, 2012) in which the induction of bnAb lineages is recreated is also used to identify other immunogens for use in the methods of the invention. It was recently demonstrated the power of mapping the co-evolution of bnAbs and founder virus for elucidating the Env evolution pathways that lead to bnAb induction (Nature 496: 469, 2013). From this type of work has come the hypothesis that bnAb induction will require a selection of antigens to recreate the “swarms” of sequentially evolved viruses that occur in the setting of bnAb generation in vivo in HIV infection (Nature 496: 469, 2013).
A critical question is why the CH505 immunogens are better than other immunogens. This rationale comes from three recent observations. First, a series of immunizations of single putatively “optimized” or “native” trimers when used as an immunogen have not induced bnAbs as single immunogens. Second, in all the chronically infected individuals who do develop bnAbs, they develop them in plasma after ˜2 years. When these individuals have been studied at the time soon after transmission, they do not make bnAbs immediately. Third, now that individual's virus and bnAb co-evolution has been mapped from the time of transmission to the development of bnAbs, the identification of the specific Envs that lead to bnAb development have been identified-thus taking the guess work out of envelope choice.
Two other considerations are important. The first is that for the CH103 bnAb CD4 binding site lineage, the VH4-59 and Vλ3-1 genes are common as are the VDJ, VJ recombinations of the lineage (Liao, Nature 496: 469, 2013). In addition, the bnAb sites are so unusual, we are finding that the same VH and VL usage is recurring in multiple individuals. Thus, we can expect the CH505 Envs to induce CD4 binding site antibodies in many different individuals.
Regarding the choice of gp120 vs. gp160, for the genetic immunization we would normally not even consider not using gp160. However, in acute infection, gp41 non-neutralizing antibodies are dominant and overwhelm gp120 responses (Tomaras, G et al. J. Virol. 82: 12449, 2008; Liao, HX et al. JEM 208: 2237, 2011). Recently we have found that the HVTN 505 DNA prime, rAd5 vaccine trial that utilized gp140 as an immunogen, also had the dominant response of non-neutralizing gp41 antibodies. Thus, we will evaluate early on the use of gp160 vs gp120 for gp41 dominance.
In certain aspects the invention provides a strategy for induction of bnAbs is to select and develop immunogens and combinations designed to recreate the antigenic evolution of Envs that occur when bnAbs do develop in the context of infection.
That broadly neutralizing antibodies (bnAbs) occur in nearly all sera from chronically infected HIV-1 subjects suggests anyone can develop some bnAb response if exposed to immunogens via vaccination. Working back from mature bnAbs through intermediates enabled understanding their development from the unmutated ancestor, and showed that antigenic diversity preceded the development of population breadth. See Liao et al. (2013) Nature 496, 469-476. In this study, an individual “CH505” was followed from HIV-1 transmission to development of broadly neutralizing antibodies. This individual developed antibodies targeted to CD4 binding site on gp120. In this individual the virus was sequenced over time, and broadly neutralizing antibody clonal lineage (“CH103”) was isolated by antigen-specific B cell sorts, memory B cell culture, and amplified by VH/VL next generation pyrosequencing. The CH103 lineage began by binding the T/F virus, autologous neutralization evolved through somatic mutation and affinity maturation, escape from neutralization drove rapid (clearly by 20 weeks) accumulation of variation in the epitope, antibody breadth followed this viral diversification.
Further analysis of envelopes and antibodies from the CH505 individual indicated that a non-CH103 Lineage (DH235=CH235) participates in driving CH103-BnAb induction. See Gao et al. (2014) Cell 158:481-491. For example, V1 loop, V5 loop and CD4 binding site loop mutations escape from CH103 and are driven by CH103 lineage. Loop D mutations enhanced neutralization by CH103 lineage and are driven by another lineage. Transmitted/founder Env, or another early envelope for example W004.26, triggers naïve B cell with CH103 Unmutated Common Ancestor (UCA) which develop in to intermediate antibodies. Transmitted/founder Env, or another early envelope for example W004.26, also triggers non-CH103 autologous neutralizing Abs that drive loop D mutations in Env that have enhanced binding to intermediate and mature CH103 antibodies and drive remainder of the lineage. In certain embodiments, the inventive composition and methods also comprise loop D mutant envelopes (e.g. but not limited to M10, M11, M19, M20, M21, M5, M6, M7, M8, M9) as immunogens. In certain embodiments, the D-loop mutants are included in an inventive composition used to induce an immune response in a subject. In certain embodiments, the D-loop mutants are included in a composition used as a prime.
The invention provides various methods to choose a subset of viral variants, including but not limited to envelopes, to investigate the role of antigenic diversity in serial samples. In other aspects, the invention provides compositions comprising viral variants, for example but not limited to envelopes, selected based on various criteria as described herein to be used as immunogens. In some embodiments, the immunogens are selected based on the envelope binding to the UCA, and/or intermediate antibodies. In some embodiments the immunogens are selected based on their chronological appearance and/or sequence diversity during infection.
In other aspects, the invention provides immunization strategies using the selections of immunogens to induce cross-reactive neutralizing antibodies. In certain aspects, the immunization strategies as described herein are referred to as “swarm” immunizations to reflect that multiple envelopes are used to induce immune responses. The multiple envelopes in a swarm could be combined in various immunization protocols of priming and boosting. Immune responses, including B cell and T cell responses, could be measured by any suitable assay and criteria, such as but non limited plasma neutralization, plasma binding to vaccine and/or heterologous envelopes and/or viruses could be measured.
In certain embodiments the invention provides that sites losing the ancestral, transmitted-founder (T/F) state are most likely under positive selection. From acute, homogenous infections with 3-5 years of follow-up, identified herein are sites of interest among plasma single genome analysis (SGA) Envs by comparing the proportion of sequences per time-point in the T/F state with a threshold, typically 5%. Sites with T/F frequencies below threshold are putative escapes. We then selected clones with representative escape mutations. Where more information was available, such as tree-corrected neutralization signatures and antibody contacts from co-crystal structure, additional sites of interest were considered.
Co-evolution of a broadly neutralizing HIV-1 antibody (CH103) and founder virus was previously reported in African donor (CH505). See Liao et al. (2013) Nature 496, 469-476. In CH505, which had an early antibody that bound autologous T/F virus, we studied 398 envs from 14 time-points over three years (median per sample: 25, range: 18-53). We found 36 sites with T/F frequencies under 20% in any sample. Neutralization and structure data identified 28 and 22 interesting sites, respectively. Together, six gp41 and 53 gp120 sites were identified, plus six V1 or V5 insertions not in HXB2.
The invention provides an approach to select reagents for neutralization assays and subsequently investigate affinity maturation, autologous neutralization, and the transition to heterologous neutralization and breadth. Given the sustained coevolution of immunity and escape this antigen selection based on antibody and antigen coevolution has specific implications for selection of immunogens for vaccine design.
In one embodiment, five envelopes were selected that represent envelope antigenic diversity. In another embodiment, six envelopes were selected that represent envelope antigenic diversity. In another embodiment, ten envelopes were selected that represent envelope antigenic diversity. These sets of envelopes represent antigenic diversity by deliberate inclusion of polymorphisms that result from immune selection by neutralizing antibodies. These selections represent various levels of antigenic diversity in the HIV-1 envelope. In some embodiments the selections are based on the genetic diversity of longitudinally sampled SGA envelopes. In some embodiments the selections are based on antigenic and or neutralization diversity. In some embodiments the selections are based on the genetic diversity of longitudinally sampled SGA envelopes, and correlated with other factors such as antigenic/neutralization diversity, and antibody coevolution.
Sequences/Clones
Described herein are nucleic and amino acids sequences of HIV-1 envelopes. The sequences for use as immunogens are in any suitable form. In certain embodiments, the described HIV-1 envelope sequences are gp160s. In certain embodiments, the described HIV-1 envelope sequences are gp120s. Other sequences, for example but not limited to stable SOSIP trimer designs, gp145s, gp140s, both cleaved and uncleaved, gp140 Envs with the deletion of the cleavage (C) site, fusion (F) and immunodominant (I) region in gp41—named as gp140ΔCFI (gp140CFI), gp140 Envs with the deletion of only the cleavage (C) site and fusion (F) domain—named as gp140ΔCF (gp140CF), gp140 Envs with the deletion of only the cleavage (C)—named gp140ΔC (gp140C) (See e.g. Liao et al. Virology 2006, 353, 268-282), gp150s, gp41s, which are readily derived from the nucleic acid and amino acid gp160 sequences. In certain embodiments the nucleic acid sequences are codon optimized for optimal expression in a host cell, for example a mammalian cell, a rBCG cell or any other suitable expression system.
An HIV-1 envelope has various structurally defined fragments/forms: gp160; gp140—including cleaved gp140 and uncleaved gp140 (gp140C), gp140CF, or gp140CFL gp120 and gp41. A skilled artisan appreciates that these fragments/forms are defined not necessarily by their crystal structure, but by their design and bounds within the full length of the gp160 envelope. While the specific consecutive amino acid sequences of envelopes from different strains are different, the bounds and design of these forms are well known and characterized in the art.
For example, it is well known in the art that during its transport to the cell surface, the gp160 polypeptide is processed and proteolytically cleaved to gp120 and gp41 proteins. Cleavages of gp160 to gp120 and gp41 occurs at a conserved cleavage site “REKR.” (SEQ ID NO: 1) See Chakrabarti et al. Journal of Virology vol. 76, pp. 5357-5368 (2002) see for example
The role of the furin cleavage site was well understood both in terms of improving cleave efficiency, see Binley et al. supra, and eliminating cleavage, see Bosch and Pawlita, Virology 64 (5):2337-2344 (1990); Guo et al. Virology 174: 217-224 (1990); McCune et al. Cell 53:55-67 (1988); Liao et al. J Virol. April; 87(8):4185-201 (2013).
Likewise, the design ofgp140 envelope forms is also well known in the art, along with the various specific changes which give rise to the gp140C (uncleaved envelope), gp140CF and gp140CFI forms. Envelope gp140 forms are designed by introducing a stop codon within the gp41 sequence. See Chakrabarti et al. at
Envelope gp140C refers to a gp140 HIV-1 envelope design with a functional deletion of the cleavage (C) site, so that the gp140 envelope is not cleaved at the furin cleavage site. The specification describes cleaved and uncleaved forms, and various furin cleavage site modifications that prevent envelope cleavage are known in the art. In some embodiments of the gp140C form, two of the R residues in and near the furin cleavage site are changed to E, e.g., RRVVEREKR (SEQ ID NO: 2) is changed to ERVVEREKE (SEQ ID NO: 3), and is one example of an uncleaved gp140 form. Another example is the gp140C form which has the REKR site (SEQ ID NO: 1) changed to SEKS (SEQ ID NO: 4). See supra for references.
Envelope gp140CF refers to a gp140 HIV-1 envelope design with a deletion of the cleavage (C) site and fusion (F) region. Envelope gp140CFI refers to a gp140 HIV-1 envelope design with a deletion of the cleavage (C) site, fusion (F) and immunodominant (I) region in gp41. See Chakrabarti et al. Journal of Virology vol. 76, pp. 5357-5368 (2002) see for example
In certain embodiments, the envelope design in accordance with the present invention involves deletion of residues (e.g., 5-11, 5, 6, 7, 8, 9, 10, or 11 amino acids) at the N-terminus. For delta N-terminal design, amino acid residues ranging from 4 residues or even fewer to 14 residues or even more are deleted. These residues are between the maturation (signal peptide, usually ending with CX, X can be any amino acid) and “VPVXXXX . . . ”. In case of CH505 T/F Env as an example, 8 amino acids (italicized and underlined in the below sequence) were deleted: MRVMGIQRNYPQWWIWSMLGFWMLMICNGMWVTVYYGVPVWKEAKTTLFCASDA KAYEKEVHNVWATHACVPTDPNPQE . . . (rest of envelope sequence is indicated as “. . . ”) (SEQ ID NO: 5). In other embodiments, the delta N-design described for CH505 T/F envelope can be used to make delta N-designs of other CH505 envelopes. In certain embodiments, the invention relates generally to an immunogen, gp160, gp120 or gp140, without an N-terminal Herpes Simplex gD tag substituted for amino acids of the N-terminus of gp120, with an HIV leader sequence (or other leader sequence), and without the original about 4 to about 25, for example 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 amino acids of the N-terminus of the envelope (e.g. gp120). See WO2013/006688, e.g. at pages 10-12, the contents of which publication is hereby incorporated by reference in its entirety.
The general strategy of deletion of N-terminal amino acids of envelopes results in proteins, for example gp120s, expressed in mammalian cells that are primarily monomeric, as opposed to dimeric, and, therefore, solves the production and scalability problem of commercial gp120 Env vaccine production. In other embodiments, the amino acid deletions at the N-terminus result in increased immunogenicity of the envelopes.
In certain embodiments, the invention provides envelope sequences, amino acid sequences and the corresponding nucleic acids, and in which the V3 loop is substituted with the following V3 loop sequence TRPNNNTRKSIRIGPGQTFY ATGDIIGNIRQAH (SEQ ID NO: 6). This substitution of the V3 loop reduced product cleavage and improves protein yield during recombinant protein production in CHO cells.
In certain embodiments, the CH505 envelopes will have added certain amino acids to enhance binding of various broad neutralizing antibodies. Such modifications could include but not limited to, mutations at W680G or modification of glycan sites for enhanced neutralization.
In certain aspects, the invention provides composition and methods which use a selection of sequential CH505 Envs, as gp120s, gp 140s cleaved and uncleaved, gp145s, gp150s and gp160s, stabilized and/or multimerized trimers, as proteins, DNAs, RNAs, or any combination thereof, administered as primes and boosts to elicit immune response. Sequential CH505 Envs as proteins would be co-administered with nucleic acid vectors containing Envs to amplify antibody induction. In certain embodiments, the compositions and methods include any immunogenic HIV-1 sequences to give the best coverage for T cell help and cytotoxic T cell induction. In certain embodiments, the compositions and methods include mosaic and/or consensus HIV-1 genes to give the best coverage for T cell help and cytotoxic T cell induction. In certain embodiments, the compositions and methods include mosaic group M and/or consensus genes to give the best coverage for T cell help and cytotoxic T cell induction. In some embodiments, the mosaic genes are any suitable gene from the HIV-1 genome. In some embodiments, the mosaic genes are Env genes, Gag genes, Pol genes, Nef genes, or any combination thereof. See e.g. U.S. Pat. No. 7,951,377. In some embodiments the mosaic genes are bivalent mosaics. In some embodiments the mosaic genes are trivalent. In some embodiments, the mosaic genes are administered in a suitable vector with each immunization with Env gene inserts in a suitable vector and/or as a protein. In some embodiments, the mosaic genes, for example as bivalent mosaic Gag group M consensus genes, are administered in a suitable vector, for example but not limited to HSV2, would be administered with each immunization with Env gene inserts in a suitable vector, for example but not limited to HSV-2.
In certain aspects the invention provides compositions and methods of Env genetic immunization either alone or with Env proteins to recreate the swarms of evolved viruses that have led to bnAb induction. Nucleotide-based vaccines offer a flexible vector format to immunize against virtually any protein antigen. Currently, two types of genetic vaccination are available for testing—DNAs and mRNAs.
In certain aspects the invention contemplates using immunogenic compositions wherein immunogens are delivered as DNA. See Graham B S, Enama M E, Nason M C, Gordon I J, Peel S A, et al. (2013) DNA Vaccine Delivered by a Needle-Free Injection Device Improves Potency of Priming for Antibody and CD8+ T-Cell Responses after rAd5 Boost in a Randomized Clinical Trial. PLoS ONE 8(4): e59340, page 9. Various technologies for delivery of nucleic acids, as DNA and/or RNA, so as to elicit immune response, both T-cell and humoral responses, are known in the art and are under developments. In certain embodiments, DNA can be delivered as naked DNA. In certain embodiments, DNA is formulated for delivery by a gene gun. In certain embodiments, DNA is administered by electroporation, or by a needle-free injection technologies, for example but not limited to Biojector® device. In certain embodiments, the DNA is inserted in vectors. The DNA is delivered using a suitable vector for expression in mammalian cells. In certain embodiments the nucleic acids encoding the envelopes are optimized for expression. In certain embodiments DNA is optimized, e.g. codon optimized, for expression. In certain embodiments the nucleic acids are optimized for expression in vectors and/or in mammalian cells. In non-limiting embodiments these are bacterially derived vectors, adenovirus based vectors, rAdenovirus (e.g. Barouch D H, et al. Nature Med. 16: 319-23, 2010), recombinant mycobacteria (e.g. rBCG or M smegmatis) (Yu, J S et al. Clinical Vaccine Immunol. 14: 886-093, 2007; ibid 13: 1204-11, 2006), and recombinant vaccinia type of vectors (Santra S. Nature Med. 16: 324-8, 2010), for example but not limited to ALVAC, replicating (Kibler K V et al., PLoS One 6: e25674, 2011 Nov. 9.) and non-replicating (Perreau M et al. J. virology 85: 9854-62, 2011) NYVAC, modified vaccinia Ankara (MVA)), adeno-associated virus, Venezuelan equine encephalitis (VEE) replicons, Herpes Simplex Virus vectors, and other suitable vectors.
In certain aspects the invention contemplates using immunogenic compositions wherein immunogens are delivered as DNA or RNA in suitable formulations. Various technologies which contemplate using DNA or RNA, or may use complexes of nucleic acid molecules and other entities to be used in immunization. In certain embodiments, DNA or RNA is administered as nanoparticles consisting of low dose antigen-encoding DNA formulated with a block copolymer (amphiphilic block copolymer 704). See Cany et al., Journal of Hepatology 2011 vol. 54 j 115-121; Arnaoty et al., Chapter 17 in Yves Bigot (ed.), Mobile Genetic Elements: Protocols and Genomic Applications, Methods in Molecular Biology, vol. 859, pp293-305 (2012); Arnaoty et al. (2013) Mol Genet Genomics. 2013 August; 288(7-8):347-63. Nanocarrier technologies called Nanotaxi® for immunogenic macromolecules (DNA, RNA, Protein) delivery are under development. See for example technologies developed by incellart.
In certain aspects the invention contemplates using immunogenic compositions wherein immunogens are delivered as recombinant proteins. Various methods for production and purification of recombinant proteins, including trimers such as but not limited to SOSIP based trimers, suitable for use in immunization are known in the art. In certain embodiments recombinant proteins are produced in CHO cells.
The immunogenic envelopes can also be administered as a protein boost in combination with a variety of nucleic acid envelope primes (e.g., HIV-1 Envs delivered as DNA expressed in viral or bacterial vectors).
Dosing of proteins and nucleic acids can be readily determined by a skilled artisan. A single dose of nucleic acid can range from a few nanograms (ng) to a few micrograms (μg) or milligram of a single immunogenic nucleic acid. Recombinant protein dose can range from a few μg micrograms to a few hundred micrograms, or milligrams of a single immunogenic polypeptide.
Administration: The compositions can be formulated with appropriate carriers using known techniques to yield compositions suitable for various routes of administration. In certain embodiments the compositions are delivered via intramascular (IM), via subcutaneous, via intravenous, via nasal, via mucosal routes, or any other suitable route of immunization.
The compositions can be formulated with appropriate carriers and adjuvants using techniques to yield compositions suitable for immunization. The compositions can include an adjuvant, such as, for example but not limited to, alum, poly IC, MF-59 or other squalene-based adjuvant, ASOIB, or other liposomal based adjuvant suitable for protein or nucleic acid immunization. In certain embodiments, the adjuvant is GSK AS01E adjuvant containing MPL and QS21. This adjuvant has been shown by GSK to be as potent as the similar adjuvant AS01B but to be less reactogenic using HBsAg as vaccine antigen [Leroux-Roels et al., IABS Conference, April 2013]. In certain embodiments, TLR agonists are used as adjuvants. In other embodiment, adjuvants which break immune tolerance are included in the immunogenic compositions.
In certain embodiments, the compositions and methods comprise any suitable agent or immune modulation which could modulate mechanisms of host immune tolerance and release of the induced antibodies. In non-limiting embodiments modulation includes PD-1 blockade; T regulatory cell depletion; CD40L hyperstimulation; soluble antigen administration, wherein the soluble antigen is designed such that the soluble agent eliminates B cells targeting dominant epitopes, or a combination thereof. In certain embodiments, an immunomodulatory agent is administered in at time and in an amount sufficient for transient modulation of the subject's immune response so as to induce an immune response which comprises broad neutralizing antibodies against HIV-1 envelope. Non-limiting examples of such agents is any one of the agents described herein: e.g. chloroquine (CQ), PTP1B Inhibitor—CAS 765317-72-4—Calbiochem or MSI 1436 clodronate or any other bisphosphonate; a Foxo1 inhibitor, e.g. 344355|Foxo1 Inhibitor, AS1842856—Calbiochem; Gleevac, anti-CD25 antibody, anti-CCR4 Ab, an agent which binds to a B cell receptor for a dominant HIV-1 envelope epitope, or any combination thereof. In non-limiting embodiments, the modulation includes administering an anti-CTLA4 antibody. Non-limiting examples are ipilimumab and tremelimumab. In certain embodiments, the methods comprise administering a second immunomodulatory agent, wherein the second and first immunomodulatory agents are different.
There are various host mechanisms that control bNAbs. For example highly somatically mutated antibodies become autoreactive and/or less fit (Immunity 8: 751, 1998; PloS Comp. Biol. 6 e1000800, 2010; J. Thoret. Biol. 164:37, 1993); Polyreactive/autoreactive naïve B cell receptors (unmutated common ancestors of clonal lineages) can lead to deletion of Ab precursors (Nature 373: 252, 1995; PNAS 107: 181, 2010; J. Immunol. 187: 3785, 2011); Abs with long HCDR3 can be limited by tolerance deletion (JI 162: 6060, 1999; JCI 108: 879, 2001). BnAb knock-in mouse models are providing insights into the various mechanisms of tolerance control of MPER BnAb induction (deletion, anergy, receptor editing). Other variations of tolerance control likely will be operative in limiting BnAbs with long HCDR3s, high levels of somatic hypermutations.
Various antibodies names are used throughout the application. Below is listing of antibodies names correlation: CH490=CH235.6; CH491=CH235.7; CH492=CH235.8; CH493=CH235.9; CH555=CH235.10; CH556=CH235.11; CH557=CH235.12. CH and DH prefixes are used interchangeably, e.g. CH235 and DH235.
It is readily understood that the envelope glycoproteins referenced in various examples and figures comprise a signal/leader sequence. It is well known in the art that HIV-1 envelope glycoprotein is a secretory protein with a signal or leader peptide sequence that is removed during processing and recombinant expression (without removal of the signal peptide, the protein is not secreted). See for example Li et al. Control of expression, glycosylation, and secretion of HIV-1 gp120 by homologous and heterologous signal sequences. Virology 204(1):266-78 (1994) (“Li et al. 1994”), at first paragraph, and Li et al. Effects of inefficient cleavage of the signal sequence of HIV-1 gp120 on its association with calnexin, folding, and intracellular transport. PNAS 93:9606-9611 (1996) (“Li et al. 1996”), at 9609. Any suitable signal sequence could be used. In some embodiments the leader sequence is the endogenous leader sequence. Most of the gp120 and gp160 amino acid sequences include the endogenous leader sequence. In other non-limiting examples the leaders sequence is human Tissue Plasminogen Activator (TPA) sequence, human CD5 leader sequence (e.g. MPMGSLQPLATLYLLGMLVASVLA (SEQ ID NO: 7)). Most of the chimeric designs include CD5 leader sequence. A skilled artisan appreciates that when used as immunogens, and for example when recombinantly produced, the amino acid sequences of these proteins do not comprise the leader peptide sequences.
Nomenclature for trimers: chim.6R.DS.SOSIP.664 is SOSIP.I CHIM.6R.SOSIP.664 is SOSIP.II; CHIM.6R.SOSIP.664V4.1 is SOSIP.III. Additional trimer designs are listed inter alia in Tables 1A-B,
The specific mutations in any one of the designs could be incorporated in any suitable envelope. For example, using as a guide the CH505 T/F designs in Tables 1A-B, CH505 M envelope can be designed as any trimer.
The invention provides various envelopes and selection of envelopes for use as immunoges, wherein the various envelope sequences and design further comprise change of amino acid position 458 form a Gly (G) to a large amino acid, e.g. but not limited to G458Y, and wherein in some embodiments the envelope has a glycosylation profile similar to the glycosylation profile of an envelope grown in GnTI−/− cells. Amino acid position G458 is with reference to the CH505 T/F envelope and a skilled artisan can readily determine the corresponding position and amino acid in other envelopes. Any one of the envelopes of the invention could be designed and expressed as described in the specification.
The invention is described in the following non-limiting examples.
HIV-1 sequences, including envelopes, and antibodies from HIV-1 infected individual CH505 were isolated as described in Liao et al. (2013) Nature 496, 469-476 including supplementary materials; See also Gao et al. (2014) Cell 158:481-491.
Recombinant HIV-1 Proteins
HIV-1 Env genes for subtype B, 63521, subtype C, 1086, and subtype CRF_01, 427299, as well as subtype C, CH505 autologous transmitted/founder Env were obtained from acutely infected HIV-1 subjects by single genome amplification, codon-optimized by using the codon usage of highly expressed human housekeeping genes, de novo synthesized (GeneScript) as gp140 or gp120 (AE.427299) and cloned into a mammalian expression plasmid pcDNA3.1/hygromycin (Invitrogen). Recombinant Env glycoproteins were produced in 293F cells cultured in serum-free medium and transfected with the HIV-1 gp140- or gp120-expressing pcDNA3.1 plasmids, purified from the supernatants of transfected 293F cells by using Galanthus nivalis lectin-agarose (Vector Labs) column chromatography, and stored at −80° C. Select Env proteins made as CH505 transmitted/founder Env were further purified by superose 6 column chromatography to trimeric forms, and used in binding assays that showed similar results as with the lectin-purified oligomers.
ELISA
Binding of patient plasma antibodies and CH103, and DH235(CH235), See Gao et al. (2014) Cell 158:481-491, clonal lineage antibodies to autologous and heterologous HIV-1 Env proteins was measured by ELISA as described previously. Plasma samples in serial threefold dilutions starting at 1:30 to 1:521,4470 or purified monoclonal antibodies in serial threefold dilutions starting at 100 μg ml-1 to 0.000 μg ml-1 diluted in PBS were assayed for binding to autologous and heterologous HIV-1 Env proteins. Binding of biotin-labelled CH103 at the subsaturating concentration was assayed for cross-competition by unlabeled HIV-1 antibodies and soluble CD4-Ig in serial fourfold dilutions starting at 10 μg ml-1. The half-maximal effective concentration (EC50) of plasma samples and monoclonal antibodies to HIV-1 Env proteins were determined and expressed as either the reciprocal dilution of the plasma samples or concentration of monoclonal antibodies.
Surface Plasmon Resonance Affinity and Kinetics Measurements
Binding Kd and rate constant (association rate (Ka)) measurements of monoclonal antibodies and all candidate UCAs to the autologous Env C. CH05 gp140 and/or the heterologous Env B.63521 gp120 are carried out on BlAcore 3000 instruments as described previously. Anti-human IgG Fc antibody (Sigma Chemicals) is immobilized on a CMS sensor chip to about 15,000 response units and each antibody is captured to about 50-200 response units on three individual flow cells for replicate analysis, in addition to having one flow cell captured with the control Synagis (anti-RSV) monoclonal antibody on the same sensor chip. Double referencing for each monoclonal antibody—HIV-1 Env binding interactions is used to subtract nonspecific binding and signal drift of the Env proteins to the control surface and blank buffer flow, respectively. Antibody capture level on the sensor surface is optimized for each monoclonal antibody to minimize rebinding and any associated avidity effects. C.CH505 Env gp140 protein is injected at concentrations ranging from 2 to 25 μg ml-1, and B.63521 gp120 was injected at 50-400 μg ml-1 for UCAs and early intermediates IA8 and IA4, 10-100 μg ml-1 for intermediate IA3, and 1-25 μg ml-1 for the distal and mature monoclonal antibodies. All curve-fitting analyses are performed using global fit of to the 1:1 Langmuir model and are representative of at least three measurements. All data analysis was performed using the BlAevaluation 4.1 analysis software (GE Healthcare).
Neutralization Assays
Neutralizing antibody assays in TZM-bl cells are performed as described previously. Neutralizing activity of plasma samples in eight serial threefold dilutions starting at 1:20 dilution and for recombinant monoclonal antibodies in eight serial threefold dilutions starting at 50 μg ml-1 are tested against autologous and herologous HIV-1 Env-pseudotyped viruses in TZM-bl-based neutralization assays using the methods known in the art. Neutralization breadth of CH103 is determined using a panel of 196 of geographically and genetically diverse Env-pseudoviruses representing the major circulated genetic subtypes and circulating recombinant forms. HIV-1 subtype robustness is derived from the analysis of HIV-1 clades over time. The data are calculated as a reduction in luminescence units compared with control wells, and reported as IC50 in either reciprocal dilution for plasma samples or in micrograms per microlitre for monoclonal antibodies.
The GenBank accession numbers for 292 CH505 Env proteins are KC247375-KC247667, and accessions for 459 VHDJH and 174 VLJL sequences of antibody members in the CH103 clonal lineage are KC575845-KC576303 and KC576304-KC576477, respectively.
Binding of Sequential Envelopes to CH103 and CH235 CD4 Binding Site bnAb Lineages Members.
The binding assay was an ELISA with the envelope protein bound to the well surface of a 96 well plate, and the antibody in questions incubated with the envelope bound to the plate. After washing, an enzyme- labeled anti-human IgG antibody was added and after incubation, washed away. The intensity of binding was determined by the intensity of enzyme-activated color in the well.
Combinations of Antigens Derived from CH505 Envelope Sequences for Swarm Immunizations
Provided herein are non-limiting examples of combinations of antigens derived from CH505 envelope sequences for a swarm immunization. Without limitations, these selected combinations comprise envelopes which provide representation of the sequence and antigenic diversity of the HIV-1 envelope variants which lead to the induction and maturation of the CH103 and CH235 antibody lineages. The identification of bnAb lineage (CH103) and envelopes which bind preferentially to various members of this lineage provides a direct strategy for the selection of Envs (out of millions possible envelopes naturally occurring in an HIV-1 infected individual) that might have engaged UCA and participated in bnAb development, and thus could serve as immunogens in a vaccine formulation. The identification of helper lineage (CH235) and envelopes which bind preferentially to various members this lineage provides a direct strategy for the selection of Envs (out of millions possible envelopes naturally occurring in an HIV-1 infected individual) that might have engaged UCA and participated in bnAb development, and thus could serve as immunogens in a vaccine formulation.
The selection includes priming with a virus which binds to the UCA, for example a T/F virus or another early (e.g. but not limited to week 004.3, or 004.26) virus envelope. In certain embodiments the prime could include D-loop variants. In certain embodiments the boost could include D-loop variants. In certain embodiments, these D-loop variants are envelope escape mutants not recognized by the UCA. Non-limiting examples of such D-loop variants are envelopes designated as M10, M11, M19, M20, M21, M5, M6, M7, M8, M9, M14 (TF_M14), M24 (TF_24), M15, M16, M17, M18, M22, M23, M24, M25, M26. See Gao et al. (2014) Cell 158:481-491.
Non-limiting embodiments of envelopes selected for swarm vaccination are shown as the selections described below. A skilled artisan would appreciate that a vaccination protocol can include a sequential immunization starting with the “prime” envelope(s) and followed by sequential boosts, which include individual envelopes or combination of envelopes. In another vaccination protocol, the sequential immunization starts with the “prime” envelope(s) and is followed with boosts of cumulative prime and/or boost envelopes. In certain embodiments, the sequential immunization starts with the “prime” envelope(s) and is followed by boost(s) with all or various combinations of the envelopes in the selection. In certain embodiments, the prime does not include T/F sequence (W000.TF). In certain embodiments, the prime includes w004.03 envelope. In certain embodiments, the prime includes w004.26 envelope. In certain embodiment the prime includes M11. In certain embodiments the prime includes M5. In certain embodiments, the immunization methods do not include immunization with HIV-1 envelope T/F. In certain embodiments, the immunization methods do not include a schedule of four valent immunization with HIV-1 envelopes T/F, w053.16, w078.33, and w100.B6.
In certain embodiments, there is some variance in the immunization regimen; in some embodiments, the selection of HIV-1 envelopes may be grouped in various combinations of primes and boosts, either as nucleic acids, proteins, or combinations thereof.
In certain embodiments the immunization includes a prime administered as DNA, and MVA boosts. See Goepfert, et al. 2014; “Specificity and 6-Month Durability of Immune Responses Induced by DNA and Recombinant Modified Vaccinia Ankara Vaccines Expressing HIV-1 Virus-Like Particles” J Infect Dis. 2014 Feb. 9. [Epub ahead of print].
HIV-1 Envelope selection A (five envelopes): M11; w020.14; w030.28; w078.15; w053.31
HIV-1 Envelope selection B (six envelopes): M11; M5; w020.14; w030.28; w078.15; w053.31
HIV-1 Envelope selection C (ten envelopes): M11; M5; w020.14; w030.28; w078.15; w053.16; w030.21; w078.33; w100.B6; w053.31.
HIV-1 Envelopes selection D (six envelopes): M5, M11, 20.14, 30.28, 30.23, 136.B18.
HIV-1 Envelopes selection E (six envelopes): M5, M11, 20.14, 30.20, 30.23, 136.B18.
HIV-1 Envelopes selection F (six envelopes—P186 study): M5, M11, 20.14, 30.20, 30.12, 136.B18.
HIV-1 envelope selection G (EnvSeq-2): M5, 30.25; 53.25; 53.29.
HIV-1 envelope selection H (EnvSeq-3): M5, 30.20; 20.14, 30.12.
HIV-1 envelope selection I: T/F, 53.16, optionally 78.33, 100.B6, or any other suitable envelope, wherein each envelope comprises G458mutation, e.g. G458Y.
Selections using M5 as a prime, e.g. but not limited to D, E, F, G or H are expected to engage receptors and drive progression of CH235 lineage of antibodies.
The selections of CH505-Envs were down-selected from a series of 400 CH505 Envs isolated by single-genome amplification followed for 3 years after acute infection, based on experimental data. The enhanced neutralization breadth that developed in the CD4-binding site (bs) CH103 antibody lineage that arose in subject CH505 developed in conjunction with epitope diversification in the CH505's viral quasispecies. It was observed that at 6 months post-infection there was more diversification in the CD4bs epitope region in this donor than sixteen other acutely infected donors. Population breadth did not arise in the CH103 antibody lineage until the epitope began to diversify. A hypothesis is that the CH103 linage drove viral escape, but then the antibody adapted to the relatively resistant viral variants. As this series of events was repeated, the emerging antibodies evolved to tolerate greater levels of diversity in relevant sites, and began to be able to recognize and neutralize diverse heterologous forms for the virus and manifest population breadth. In certain embodiments, six envs are selected from CH505 sequences to reflect diverse variants for making Env pseudoviruses, with the goal of recapitulating CH505 HIV-1 antigenic diversity over time, making sure selected site (i.e. those sites reflecting major antigenic shifts) diversity was represented.
Specifically, for CH505 the virus and envelope evolution were mapped, and the CH103 CD4 binding-site bnAb evolution. In addition, 135 CH505 varied envelope pseudotyped viruses were made and tested them for neutralization sensitivity by members of the CH103 bnAb lineage (e.g,
In certain embodiments, the envelopes are selected based on Env mutants with sites under diversifying selection, in which the transmitted/founder (T/F) Env form vanished below 20% in any sample, i.e. escape variants; signature sites based on autologous neutralization data, i.e. Envs with statistically supported signatures for escape from members of the CH103 bnAb lineage; and sites with mutations at the contact sites of the CH103 antibody and HIV Env. In this manner, a sequential swarm of Envs was selected for immunization to represent the progression of virus escape mutants that evolved during bnAb induction and increasing neutralization breadth in the CH505 donor.
In certain embodiments, additional sequences are selected to contain five additional specific amino acid signatures of resistance that were identified at the global population level. These sequences contain statistically defined resistance signatures, which are common at the population level and enriched among heterologous viruses that CH103 fails to neutralize. When they were introduced into the TF sequence, they were experimentally shown to confer partial resistance to antibodies in the CH103 lineage. Following the reasoning that serial viral escape and antibody adaptation to escape is what ultimate selects for neutralizing antibodies that exhibit breadth and potency against diverse variants, in certain embodiments, inclusion of these variants in a vaccine may extend the breadth of vaccine-elicited antibodies even beyond that of the CH103 lineage. Thus the overarching goal will be to trigger a CH103-like lineage first using the CH505TF modified M11, that is well recognized by early CH103 ancestral states, then vaccinating with antigenic variants, to allow the antibody lineage to adapt through somatic mutation to accommodate the natural variants that arose in CH505. In certain embodiments, vaccination regimens include a total of five sequences (Selection A) that capture the antigenic diversity of CH505. In another embodiment, additional antigenic diversity is added (Selection B and C), to enable the induction of antibodies by vaccination that may have even greater breadth than those antibodies isolated from CH505.
In some embodiments, the CH505 sequences that represent the accumulation of viral sequence and antigenic diversity in the CD4bs epitope of CH103 in subject CH505 are represented by selection A, selection B, or selection C.
M11 is a mutant generated to include two mutations in the loop D (N279D+V281G relative to the TF sequence) that enhanced binding to the CH103 lineage. These were early escape mutations for another CD4bs autologous neutralizing antibody lineage, but might have served to promote early expansion of the CH103 lineage.
In certain embodiments, the two CH103 resistance signature-mutation sequences added to the antigenic swarm are: M14 (TF with S364P), and M24 (TF with S375H+T202K+L520F+G459E). They confer partial resistance to the TF with respect to the CH103 lineage. In certain embodiments, these D-loop mutants are administered in the boost.
Immunization Protocols in Subjects with Swarms of HIV-1 Envelopes.
Immunization protocols contemplated by the invention include envelopes sequences as described herein including but not limited to nucleic acids and/or amino acid sequences of gp160s, gp150s, gp145, cleaved and uncleaved gp140s, stabilized trimers, e.g. but not limited to SOSIP trimers, gp120s, gp41s, N-terminal deletion variants as described herein, cleavage resistant variants as described herein, or codon optimized sequences thereof. A skilled artisan can readily modify the gp160 and gp120 sequences described herein to obtain these envelope variants. The swarm immunization selections can be administered in any subject, for example monkeys, mice, guinea pigs, or human subjects.
In non-limiting embodiments, the immunization includes a nucleic acid which is administered as DNA, for example in a modified vaccinia vector (MVA). In non-limiting embodiments, the nucleic acids encode gp160 envelopes. In other embodiments, the nucleic acids encode gp120 envelopes. In other embodiments, the boost comprises a recombinant gp120 envelope. The vaccination protocols include envelopes formulated in a suitable carrier and/or adjuvant, for example but not limited to alum. In certain embodiments the immunizations include a prime, as a nucleic acid or a recombinant protein, followed by a boost, as a nucleic acid or a recombinant protein. A skilled artisan can readily determine the number of boosts and intervals between boosts.
In some embodiments, the immunization methods comprise immunization prime with a nucleic acid, for example but not limited to priming two times with DNA. In some embodiments the nucleic acid prime is administered one, two, three or four times. In some embodiments the two DNA prime is administered via electroporation (DNA-EP). In some embodiments, the primer and boost is administered as RNA. The primes are followed by boost with sequential envelopes. The boosting envelopes could be in any suitable form, e.g. but not limited to gp140s, as soluble or stabilized SOSIP trimers.
Table 6 shows a non-limiting example of an immunization protocol using a selection of HIV-1 envelopes
Table 7 shows a non-limiting example of an immunization protocol using a selection of HIV-1 envelopes
In certain embodiments, after administering a prime with M11, subsequent immunizations include all other envelopes as nucleic acids and/or proteins.
Table 8 shows a non-limiting example of an immunization protocol using a swarm of HIV-1 envelopes
Table 9 shows a non-limiting example of an immunization protocol using a swarm of HIV-1 envelopes
In certain embodiments, after administering a prime with M11 and optionally with M5, subsequent immunizations include all other envelopes as nucleic acids and/or proteins.
Table 10 shows a non-limiting example of immunization protocol using a selection of ten HIV-1 envelopes
Table 11 shows a non-limiting example of immunization protocol using a selection of six HIV-1 envelopes
Table 12 shows a non-limiting example of immunization protocol using a selection of six HIV-1 envelopes
In certain embodiments, after administering a prime with M11 and optionally with M5, subsequent immunizations include sequential or cumulative addition of the other envelopes as nucleic acids and/or proteins.
Table 13 shows a non-limiting example of immunization protocol using a selection of four HIV-1 envelopes
In certain embodiments an immunization protocol could prime with a bivalent or trivalent Gag mosaic (Gag 1 and Gag 2, Gag 1, Gag 2 and Gag3) in a suitable vector.
Env Mixtures of the CH505 Virus are Expected to Induce the Beginning of CD4 Binding Site BnAb Lineages CH103 and CH235
The combinations of envelopes described in Examples 2-4 will be tested in any suitable subject. Suitable animal models include without limitation mice, including humanized mice, guinea pigs, or non-human primates (NHPs). For example an animal is administered with the following antigens, as DNA and/or proteins, in any suitable for, in the following immunization schedule: loop D mutant M5 and/or M11. That will give the best CH103 UCA binder (M11) and the best CH235 UCA binder (M5). Immunization 2: week 020.14. Immunization 3: Week 030.28. Immunization 4: week 078.15. Immunization 5: week 100.B6. Immunization 5: swarm of all six envelopes. Adjuvant is a TLR-4 agonist (GLA-synthetic monophosphoryl lipid A) in stable emulsion from Infectious Disease Research Institute, Seattle Wash.
In another embodiment, the prime is M5 and M11. The boost includes 20.14, 30.20, 30.12, and 136.B18, sequentially or additively.
Immunization Elicits Heterologous and Autologous Tier 2 Neutralizing Antibodies.
While improved breadth of vaccine-induced neutralizing antibody responses against tier 2 viruses are needed for a protective HIV-1 vaccine, elicitation of bnAbs by vaccination has proven challenging.
This example shows elicitation of heterologous and autologous tier 2 neutralizing antibodies with sequential Env vaccination in rhesus macaques. See also
Co-evolution studies of the CH103 lineage of antibodies and viruses from the same infected person CH505 provides a roadmap for how bnAbs develop during natural infection (Liao et al. Nature 2014; Bonsignori et al. Cell 2016).
This animal study compared the immunogenicity of CH505 gp140C oligomers to CH505-CD40 conjugates. We hypothesize that a roadblock to bnAb induction by vaccination is the lack of B cell stimulation by antigen presenting cells (dendritic cells and monocytes), and that bNAbs, similar to those in the CH103 bnAb lineage, can be induced by vaccination with sequential Envs from CH505 (TF, w053.16, w078.33 and w100.B6). In this experiment the T/F envelope was administered as a DNA prime. In some animals the boosting envelopes (TF, w053.16, w078.33 and w100.B6) were administered as gp140C envelopes. In some animals these envelopes were targeted to antigen presenting cells by a CD40 antibody—human anti-CD40 IgG4 was linked to the CH505 gp140C.
It is possible that the reduced immunogenicity of the anti-CD40 IgG4-CH505 Env regimen is due to anti-drug antibodies in rhesus macaques.
This example shows that: DNA-EP prime and gp140C oligomer boosts induced autologous tier 2 neutralization in 1 of 4 macaques; heterologous tier 2 neutralization of 9/12 tier 2 isolates was also elicited in the same macaque; and that CD4 binding site directed plasma IgG was present in wildtype Env immunized macaques. RSC3-reactive B cells were sorted from macaques and the binding and neutralization screening is ongoing.
This example demonstrated that sequential Env immunogens , including the sequential immunogens used in this study could induce heterologous Tier 2 neutralizatoin. One alternative to increase the response rate of bnAb induction is the use of sequential near-native soluble CH505 trimers (e.g. but not limited to SOSIP based trimers as described herein). Immunization with CH505 stabilized trimers while modulating immune tolerance with immune checkpoint inhibitors is also underway.
In some embodiments, the immunization methods could comprise immunization prime with a nucleic acid, for example but not limited to priming two times with DNA, In some embodiments the nucleic acid prime is administered one, two, three or four times. In some embodiments the two DNA prime is administered via electroporation (DNA-EP). In some embodiments the nucleic acid encodes any suitable form of the envelope. In some embodiments, the primer and boost is administered as RNA. The primes are followed by boost with sequential envelopes. The boosting envelopes could be in any suitable form, e.g. but not limited to gp140s, as soluble or stabilized SOSIP trimers, e.g. but not limited to SOSIP.III.
Over the past five years, the HIV vaccine development field has realized that immunization with a single HIV envelope protein will not be successful at inducing bnAbs1,2. Moreover, with evidence for a role of host immune tolerance control mechanisms in limiting the induction of bnAbs1,3, the biology of bnAbs has begun to be elucidated. The role of the structure of the Env immunogen is undoubtedly important, as the Env must contain sufficiently native bnAb epitopes to bind in optimal affinities to the unmutated common ancestor (UCA, naïve B cell receptors) of bnAb lineages2,4. Thus, the concept of B cell lineage immunogen design has arisen, whereby lineages of bnAbs are elucidated, and Envs chosen for sequential immunizations based on optimized affinity of Env immunogens for BCRs at sequential steps of the affinity maturation pathway of bnAb lineages2
While Envs have been designed for reacting with UCAs of heterologous bnAb lineages4,5, we have taken the approach of defining, in select HIV-infected individuals who make bnAbs, the natural sequence of Envs that induced the bnAb lineages in order to make immunogen down selection an evidence-based decision. While such immunogens are designed for the UCA and intermediate antibodies of one particular bnAb lineage, they hold promise for inducing bnAb lineages in multiple individuals because of the remarkable conserved usage of VH and VL genes of bnAbs and the restricted nature of antibody motifs for many bnAb types, particularly for the gp41 membrane proximal region6, the CD4 binding site7 and the V1V2-glycan site1,8-10.
Two Types of CD4 Binding Site Antibodies
There are several types of CD4 binding site (bs) bnAbs two of which are a) heavy chain complementarity determining region 3 (HCDR3) binders and b) CD4 mimicking bnAbs7. HCDR3 binding CD4 binding site bnAbs approach the CD4 binding site with the HCDR3 and other VH and VL loops with multiple loop-based interactions. Several different VHs and VLs are used by HCDR3 binding bnAbs with VH3 and VH4 the most common. In contrast, CD4 mimicking bnAbs have restricted VH usage and either use VH1-2*02 or VH1-46. When VH1-2*02 is used, the light chain LCDR3 must be five amino acids in length. However, when VH1-46 is used, the LCDR3 can be of normal (10-13 aa) in length. Both VH1-2*02 and VH1-46 CD4 mimicking antibodies approach the CD4 binding site in a highly homologous manner to the approach of CD4, and structural analysis of such bnAbs demonstrates both structural similarity to CD4, as well as near identical structures to each of these types of antibodies7. Finally, HCDR3 binders are less broad and potent than CD4 mimicking antibodies, with HCDR3 binders neutralizing ˜50% of isolates (e.g., CH103, CH98) while CD4 mimickers neutralizing 90-95% of isolates (e.g., CH235.12, VRC01)7. Thus, both types of antibodies are desirable to induce with vaccination as components of a polyclonal bnAb response.
The CH505 African HIV-infected individual that makes both types of CD4bs bnAbs over 6 years (See Liao et al. (2013) Nature 496, 469-476 including supplementary materials; See also Gao et al. (2014) Cell 158:481-491; Example 8)
Thus, from African individual CH505, we have isolated both sequential Envs and bnAbs over time, and mapped the co-evolution of two bnAb lineages, the CH103 CD4 binding site HCDR3 binder bnAb lineage11 and the CH235 CD4 mimicking CD4bs VH1-46 bnAb lineage12. The CH103 HCDR3 binder type of CD4 binding site antibody achieved 55% maximum breadth and 4.5 mcg inhibitory concentration 50 (IC50) neutralization of cross-clade HIVs11. In contrast, the CH235 CD4 mimicking CD4 binding site antibody achieved 90% neutralization and neutralizing IC50 of 0.7 mcg/ml. Here, we will describe the work of development of sequential Env regimens to induce both of these types of bnAb lineages, and propose here the new sequential Envs to specifically initiate CH235-like CD4 mimicking bnAb lineages.
The EnvSeq-1 Sequential Vaccine from CH505 Designed to Induce HCDR3-Type of CD4 Binding Site bnAbs
We have developed a 4-valent immunogen comprised of CH505 envelopes that have been designed to trigger the CH103 lineage UCA to clonally expand and start off CH103-like CD4bs HCDR3-binder types of B cell lineages (TF; w053.16; w078.33; w100.B6 the EnvSeq-1 vaccine, see WO2014042669 incorporated by reference in its entirety). In SPR assays, the transmitted/founder (T/F) Env gp120 reacted with the UCA of the CH103 lineage with a KD of ˜200 nM. Studies in CH103 VH+VL knock-in mice and Rhesus macaques using EnvSeq-1 have been completed and demonstrate proof of concept that sequential CH505 gp120s can initiate bnAb B cell clonal lineages in the setting of vaccination. The EnvSeq-1 vaccine binds to CH103 precursors in CH103 bnAb knock-in mice and can expand them with immunization in adjuvant. In Rhesus macaques, the gp120 EnvSeq-1 vaccine can induce antibodies with the characteristics of precursors of CD4 binding site bnAbs. These characteristics include antibodies that differentially bind CH505 Env but not Env with an isoleucine deletion at aa 371 that disrupts the CD4 binding site, antibodies that use similar VH4 and V13 genes to the human CH103 bnAb, and antibodies that neutralize the tier lb T/F variant CH505 4.3 as well as some tier 2 viruses.
Utility of gp120s as Sequential Envs
Whether a native trimer is needed for this purpose or if a highly antigenic Env subunit will suffice is yet unknown, but studies in mice in basic B cell biology have demonstrated that what is important for B cell survival in the germinal center (GC) is the optimal affinity of the immunogen for the GC B cell receptor (BCR)13,14. A key question is whether gp120 or gp140 trimers are preferred immunogens in a sequential regimen. Emerging data have demonstrated that gp120s or their fragments can engage bnAb UCAs and expand CD4bs bnAb precursors5,15,16. In contrast, recent data with soluble individual trimers have demonstrated that they have only induced autologous tier 2 neutralizing antibodies against glycan-bare spots and not bnAb epitopes17,18. Thus, it is appropriate at this time to continue to study gp120 immunogens in man to test the hypothesis that sequential immunogens can initiate bnAb lineages. Whether boosting later in the immunization sequence with a trimeric Env will be needed will be tested in future studies.
The EnvSeq-2 Sequential Vaccine from CH505 is Designed to Induce CD4 Mimicking-Type of CD4 Binding Site bnAbs
In this application we propose to extend the test of sequential Env immunizations in man for initiation of broadly neutralizing antibodies to test in a human Phase I clinical trial of a new series of CH505 Envs (the EnvSeq-2 vaccine) specifically designed to induce a broader and more potent bnAb type, the CH235-like VH1-46 utilizing CD4 mimicking broad neutralizing antibody with 90% breadth and 0.6 mcg/ml inhibitory concentration 50 (IC50).
Design of a Sequential Immunogen (EnvSeq-2) to Initiate VH1-46 CD4 Mimicking CD4 Binding Site Antibody Lineages
Provided herein is a new set of immunogens based on the recent work describing the sequence of events that occurred with the development of CD4 mimicking CD4 binding site bnAb lineage, CH23512.
From this work, a natural mutant of the CH505 T/F Env called CH505.M5 was found with one amino acid difference than the CH505 T/F strain, i.e., a single N279K change, that occurred very early on after infection; M5 binds to the CH235 UCA (˜0.5 micromolar)3. Thus, M5 is the initiating Env for CD4 mimicking CD4 binding site antibodies in the context of the EnvSeq-2 vaccine.
Next, a set of 6 mutations at amino acids 97, 275, 278, 279, 281, and 471 in the Env binding site to the CH235 lineage (
Importantly, the later CH235 antibody lineage members acquired the ability to recognize viruses with these 6 Env mutations, presumably due to the selection imposed by exposure to the resistance mutations in vivo. These late Ch235 antibodies (such as the most potent CH235.12 antibody) had expanded breadth due to selection for recognition of these 6 mutations.
These chosen Envs in EnvSeq-2 vaccine are not associated with the best binding of the antibodies at intermediate steps as was done for design of the EnvSeq-1 vaccine above. Rather, as the increase in breadth at in the heterologous panel coincided with a gained capacity to recognize resistance mutations, Envs were selected based on their potential to expand CH235 antibody lineage recognition in order to tolerate these 6 key and common neutralization resistance-Env mutations. Nonetheless the selected Envs indeed had capacity to sequentially bind to lineage members (
Finally, the fifth hypervariable loop (V5) region length was also a strong signature for recognition of CH505 viruses by CH235 antibodies, and early lineage members could only bind and neutralize short V5s. Longer V5s were selected by the early antibodies, and later antibodies could recognize viruses with longer V5s, which are more representative of the heterologous tier 2 HIV virus population. Thus, a final key criterion for selection of sequential Envs in the EnvSeq-2 vaccine was progressive lengthening of V5 (Table 14). Thus, the EnvSeq-2 Envs are associated with development of heterologous breadth from the CH235 UCA->CH235->CH235.9->CH235.12.
The EnvSeq-2 set of immunogens are currently begin produced in non-GMP in pre-production runs, and during year 1 of the Staged Vaccine Contract, will be tested in vitro in recombinant protein immunizations in both VH+VL humanized mice and rhesus macaques. In addition, a second set of CH505 immunogens chosen based on affinity of binding to members of the CH235 antibody lineage will be tested in similar immunization studies (a vaccine called EnvSeq-3,
The optimal immunogen of the two sets of sequential Envs following comparison of EnvSeq-2 versus EnvSeq-3 will be chosen for GMP production in preclinical studies based on the following criteria:
In summary, provided are two selections of CH505 envelopes—
Four CH505 Vaccine Candidates Based on the Evolution of Breadth of the CH235 Lineage, Targeting the CD4bs
The mutant called CH505.M5 is the starting point for identifying CH505 vaccine candidates. CH505.M5 is one amino acid different than the CH505 TF strain, with a single N279K change, that occurred very early and conferred resistance to the cooperating CH103 lineages.
Identification of Signature Sites in the Contact Surface of the Antibody (<8.5 A)
Mutational patterns in the signature sites in the contact surface of the antibody are determined (in the global Tier II panel, as well as in our subjects). These sites are related to heterologous and autologous neutralization sensitivity/resistance signatures. The pattern of critical interest is the set of mutations (in this case, 6 positions with mutations that are common in the circulating population) that were associated with a high degree of resistance in the heterologous population to early CH235 lineage members, but that were less restrictive for late lineage members. These amino acids were also associated with a high degree of resistance to early antibodies among CH505's Envs, and so escape in the autologous population. Later lineage members acquired the ability to recognize these mutations, presumably due to the selection imposed by exposure to the resistance mutations in vivo. These late antibodies then had expanded breadth at the population level, presumably due to selection for recognition of these mutations.
These amino acids are not associated with the best binding of the antibodies at intermediate steps (earlier hypotheses for selecting Envs was to simply pick those that bound best to intermediate linage members). As the increase in breadth in the heterologous panel coincides with a gained capacity to recognize resistance mutations, Envs are picked based on their potential to expand Ab recognition to tolerate common resistance mutations and also to require Envs that had at least some capacity to bind to lineage members, but placing emphasis on covering common signatures, not on highest binders.
Hypervariable V5 region length was also a strong signature for recognition, and early lineage members could only see short V5's. Longer V5s were selected by the early antibodies, and later antibodies could recognize viruses with longer V5s, which are more representative of the heterologous population.
The mutations conferring viral escape (or relative resistance) from early lineage antibodies are educating the later antibodies.
Later antibodies in the lineage gain breadth at the population level because they evolved the capacity to recognize particular resistance conferring amino acids that arose in vivo.
Envs that are associated with jump in breadth from the UCA->CH235->CH235.9->CH235.12 are defined. The amino acids that are statistically most closely associated with distinct increases in breadth, the heterologous signatures, are identified. These signatures are related back to cycles of escape/recognition in vivo—exposure to these signature amino acids seems to trigger the increase breadth.
Mutations that are common in the circulating population and are heterologous signatures are shown on the right of
Envs from CH505 that carried the signature mutations were picked, requiring at least some binding of later antibodies to the antigens and that they carried modest increases in V5 length relative to M5 (
Although CH235.12 binds Envs that carry K97E and G471E with low affinity, the differential capacity to recognize heterologous Envs between CH235.9 and CH235.12 is very strongly associated with CH235.12's ability to recognize Envs that have an E in either one of those 2 positions, so including them here may enable selection of antibodies that can recognize these quite common mutations at the population level, that restrict CH235's early lineage member's breadth (
A main difference between the choice of CH505 immunogens in
The immunogens of the invention, for example Selection F (M5, M11, 20.14, 30.20, 30.12, 136.B18) could be tested in any suitable non-human animal model. Immune responses, including B cell and T cell responses to the vaccine, could be measured by any suitable assay and criteria, such as but non limited plasma neutralization, plasma binding to vaccine and/or heterologous envelopes and/or viruses could be measured. Animals studies with various forms of the selected immunogens are contemplated: gp160 mRNA of M5, M11, 20.14, 30.20, 30.12, 136.B18 (NHP #141), 6-valent M5, M11, 20.14, 30.20, 30.12, 136.B18 as SOSIP trimers (NHP #142), mRNA of 6-valent stabilized SOSIP trimers of M5, M11, 20.14, 30.20, 30.12, 136.B18 (NHP #140), gp145DNA of CH505M5 and CH505M11 as a prime and a subsequence boost(s), followed by 6-valent M5, M11, 20.14, 30.20, 30.12, 136.B18 SOSIP trimers (e.g. NHP #139). In some embodiments the SOSIP trimer is SOSIP v4.1. Any other trimer design is contemplated. Any suitable adjuvant could be used. Studies could be performed in any suitable animal model. Studies could be performed in adults and neonates.
In any of the methods of the invention, the mRNA immunogens are delivered by a lipid nanoparticle (LNP) technology. The LNPs comprises four different lipids that could self assemble to 80-100 nm size particles.
This protocol describes NHP immunization study with M5, M11, 20.14, 30.20, 30.12, 136.B18 envelopes and SIVGag. In some embodiments the below vaccination regimen could be carried out with the proteins delivered as trimers, for example but not limited to SOSIP.III trimers.
Non-limiting example of an immunization protocols with Selection F (M5, M11, 20.14, 30.20, 30.12, 136.B18). In this example the immunogens are delivered as mRNA formulated in nanoparticles. In some embodiments the stabilized trimers are of the design SOSIP.III.
Materials needed: Formulate mRNA for 6 monkeys. 6 doses×50 ug/nhp=300 ug of each mRNA construct.
Collections of Plasma, Serum, and PBMC: Collect all plasma and serum in 250 uL aliquots and save all PBMCs. CBC collection: 850 uL from each animal
Animal studies using the above protocols could be carried out with the immunogens of Selection G (EnvSeq-2), or Selection H (EnvSeq-3).
Animal studies with envelopes CH505 T/F, as stable trimers are also contemplated. Non-limiting examples of such studies include: CH505 T/F as gp145 nucleic acid prime (once or twice), followed by sequential SOSIP 4.1 trimers of CH505 T/F, CH505 w53.16, CH505 w78.33, CH505 w100.B6. In some embodiments there is no nucleic acid prime and immunization regimen comprises sequential SOSIP 4.1 trimers of CH505 T/F, CH505 w53.16, CH505 w78.33, CH505 w100.B6. In some embodiments the nucleic acid is mRNA. In some embodiments the nucleic acid is DNA. In some embodiments the DNA is administered via electroporation. In some embodiments of these studies, animals could be boosted with CH505 w136.B8.
Antibodies with ontogenies from VH1-2 or VH1-46-germline genes dominate the broadly neutralizing response against the CD4-binding site (CD4bs) on HIV-1. Here we define with longitudinal sampling from time-of-infection the development of a VH1-46-derived antibody lineage that matured to neutralize 90% of HIV-1 isolates. Structures of lineage antibodies CH235 (week 41 from time-of-infection, 18% breadth), CH235.9 (week 152, 77%) and CH235.12 (week 323, 90%) demonstrated the maturing epitope to focus on the conformationally invariant portion of the CD4bs. Similarities between CH235 lineage and five unrelated CD4bs lineages in epitope focusing, length-of-time to develop breadth, and extraordinary levels of somatic hypermutation suggested commonalities in maturation among all CD4bs antibodies. Fortunately, the required CH235-lineage hypermutation appeared substantially guided by the intrinsic mutability of the VH1-46 gene, which closely resembled VH1-2. We integrated our CH235-lineage findings with a second broadly neutralizing lineage and HIV-1 co-evolution to suggest a vaccination strategy for inducing both lineages. See Cell. 2016 Apr. 7; 165(2):449-63. GenBank Accession numbers of the CH235UCA heavy and light chains are KU570032.1 and KU570045.1
Accession Numbers
Coordinates and structure factors for CH235, CH235.9 and CH235.12 in complex with HIV-1 gp120 have been deposited with the Protein Data Bank (PDB ID 5F9W, 5F9O and 5F96). Next-generation sequencing data have been deposited with the NCBI Sequence Reads Archive (SRP067168). Antibody heavy and light chains have been deposited with GenBank (KU570032-KU570053).
Antibodies Names Correlation: See supra.
This example shows that stabilized HIV-1 Env trimer immunogens show enhanced antigenicity for broadly neutralizing antibodies, and are not recognized by non-neutralizing antibodies. See also
A stabilized chimeric SOSIP.III design was used to generate 10 CH505 trimers. The CH505 TF SOSIP.III bound the CH103 UCA. Binding affinity of the CH103 lineage to the CH505 TF SOSIP.III correlates with neutralization potency against CH505 TF virus. This design was applicable to diverse viruses from multiple clades.
These results indicate that the native trimer on virions could have initiated the CH103 lineage during natural infection. CH103 recognizes all three protomers on the Env trimer. The SOSIP.III mimicked the native trimer on the virion in that stronger binding to it correlated with neutralization potency for the CH103 lineage. The SOSIP.III design enables soluble mimics of the native trimer to be tested as sequential immunogens in CH505 B cell lineage design vaccination. These trimers enable our efforts to utilize B cell lineage design with trimeric immunogens.
Elicitation of neutralizing antibodies is one goal for antibody-based vaccines. Neutralizing antibodies target the native trimeric HIV-1 Env on the surface virions. The trimeric HIV-1 envelope protein consists of three protomers each containing a gp120 and gp41 heterodimer. Recent immunogen design efforts have generated soluble near-native mimics of the Env trimer that bind to neutralizing antibodies but not non-neutralizing antibodies. The recapitulation of the native trimer could be a key component of vaccine induction of neutralizing antibodies. Neutralizing Abs target the native trimeric HIV-1 Env on the surface of viruses (Poignard et al. J Virol. 2003 January; 77(1):353-65; Parren et al. J Virol. 1998 December; 72(12):10270-4; Yang et al. J Virol. 2006 November; 80(22):11404-8.). The HIV-1 Env protein consists of three protomers of gp120 and gp41 heterodimers that are noncovalently linked together (Center et al. J Virol. 2002 August; 76(15):7863-7.). Soluble near-native trimers preferentially bind neutralizing antibodies as opposed to non-neutralizing antibodies (Sanders et al. PLoS Pathog. 2013 September; 9(9): e1003618).
Sequential Env vaccination has elicited broad neutralization in the plasma of one macaque (Example 5B). The overall goal of our project is to increase the frequency of vaccine induction of bnabs in the plasma of primates with sequential Env vaccination. We hypothesized that vaccination with sequential immunogens that target bnAb B cell lineage and mimic native trimers will increase the frequency of broadly neutralizing plasma antibodies. One goal is increase the frequency of vaccine induction of bnAb in the plasma of primates by sequential Env vaccination. It is expected that vaccination with sequential immunogens that target bnAb B cell lineages and mimic the native trimers on virions will increase the frequency of broadly neutralizing plasma antibodies.
Previous work has shown that CH505 derived soluble trimers are hard to produce. From a study published by Julien et al in 2015 (Proc Natl Acad Sci USA. 2015 Sep. 22; 112(38): 11947-11952.) it was shown that while CH505 produced comparable amounts of protein by transient transfection, only 5% of the CH505 protein formed trimer which 5 times lower than the gold standard viral strain BG505. Provided here are non-limiting embodiments of well-folded trimers for Env immunizations.
Near-native soluble trimers using the 6R.SOSIP.664 design are capable of generating autologous tier 2 neutralizing plasma antibodies in the plasma (Sanders et al. 2015), which provides a starting point for designing immunogens to elicit broadly neutralizing antibodies. While these trimers are preferentially antigenic for neutralizing antibodies they still possess the ability to expose the V3 loop, which generally results in strain-specific binding and neutralizing antibodies after vaccination. Using the unliganded structure the BG505.6R.SOSIP.664 has been stabilized by adding cysteines at position 201 and 433 to constrain the conformational flexibility such that the V3 loop is maintained unexposed (Kwon et al. Nat Struct Mol Biol. 2015 July; 22(7): 522-531.).
Immunogen design. Provided are engineered trimeric immunogens derived from multiple viruses from CH505. We generated chimeric 6R.SOSIP.664, chimeric disulfide stabilized (DS) 6R.SOSIP.664 (Kwon et al Nat Struct Mol Biol. 2015 July; 22(7): 522-531.), chimeric 6R.SOSIP.664v4.1 (DeTaeye et al. Cell. 2015 Dec. 17; 163(7):1702-15. doi: 10.1016/j.cell.2015.11.056), and chimeric 6R.SOSIP.664v4.2 (DeTaeye et al. Cell. 2015 Dec. 17; 163(7):1702-15. doi: 10.1016/j.cell.2015.11.056). The 6R.SOSIP.664 is the basis for all of these designs and is made as a chimera of C.CH0505 and A.BG505. The gp120 of C.CH505 was fused with the BG505 inner domain gp120 sequence within the alpha helix 5 (α5) to result in the chimeric protein. The chimeric gp120 is disulfide linked to the A.BG505 gp41 as outlined by Sanders et al. (PLoS Pathog. 2013 September; 9(9): e1003618). These immunogens were designed as chimeric proteins that possess the BG505 gp41 connected to the CH505 gp120, since the BG505 strain is particularly adept at forming well-folded, closed trimers (
Recombinant envelopes as trimers could be produced and purified by any suitable method. For a non-limiting example of purification methods see Ringe R P, Yasmeen A, Ozorowski G, Go E P, Pritchard L K, Guttman M, Ketas T A, Cottrell C A, Wilson I A, Sanders R W, Cupo A, Crispin M, Lee K K, Desaire H, Ward A B, Klasse P J, Moore J P. 2015. Influences on the design and purification of soluble, recombinant native-like HIV-1 envelope glycoprotein trimers. J Virol 89:12189 -12210. doi:10.1128/JVI.01768-15.
Multimeric Envelopes
Presentation of antigens as particulates reduces the B cell receptor affinity necessary for signal transduction and expansion (See Baptista et al. EMBO J. 2000 Feb. 15; 19(4): 513-520). Displaying multiple copies of the antigen on a particle provides an avidity effect that can overcome the low affinity between the antigen and B cell receptor. The initial B cell receptor specific for pathogens can be low affinity, which precludes vaccines from being able to stimulate and expand B cells of interest. In particular, very few naïve B cells from which HIV-1 broadly neutralizing antibodies arise can bind to soluble HIV-1 Envelope. Provided are envelopes, including but not limited to trimers as particulate, high-density array on liposomes or other particles, for example but not limited to nanoparticles. See e.g. He et al. Nature Communications 7, Article number: 12041 (2016), doi:10.1038/ncomms12041; Bamrungsap et al. Nanomedicine, 2012, 7 (8), 1253-1271.
To improve the interaction between the naïve B cell receptor and CH505 SOSIP trimer protein we created to two constructs that can be presented on particles. The first construct was made by fusing HIV-1 Envelope trimer CH505 to ferritin (See
Another approach to multimerize expression constructs uses staphylococcus Sortase A transpeptidase ligation to conjugate CH505 envelope trimers to cholesterol. The CH505 trimers can then be embedded into liposomes via the conjugated cholesterol. To conjugate the CH505 trimer to cholesterol either a C-teminal LPXTG tag (SEQ ID NO: 396) or a N-terminal pentaglycine repeat tag (SEQ ID NO: 307) was added to the CH505 envelope trimer gene. Cholesterol was also synthesized with these two tags. Sortase A was then used to covalently bond the tagged CH505 envelope to the cholesterol. The sortase A-tagged trimer protein can also be used to conjugate the trimer to other peptides, proteins, or fluorescent labels.
The invention provides design of envelopes and trimer designs wherein the envelope comprises a linker which permits addition of a lipid, such as but not limited to cholesterol, via a Sortase A reaction. See e.g. Tsukiji, S. and Nagamune, T. (2009), Sortase-Mediated Ligation: A Gift from Gram-Positive Bacteria to Protein Engineering. ChemBioChem, 10: 787-798. doi:10.1002/cbic.200800724; Proft, T. Sortase-mediated protein ligation: an emerging biotechnology tool for protein modification and immobilisation. Biotechnol Lett (2010) 32: 1. doi:10.1007/s10529-009-0116-0; Lena Schmohl, Dirk Schwarzer, Sortase-mediated ligations for the site-specific modification of proteins, Current Opinion in Chemical Biology, Volume 22, October 2014, Pages 122-128, ISSN 1367-5931, dx.doi.org/10.1016/j.cbpa.2014.09.020; Tabata et al. Anticancer Res. 2015 August; 35(8):4411-7.
The lipid modified envelopes and trimers could be formulated as liposomes. Any suitable liposome composition is contemplated.
Non-limiting embodiments of envelope designs for use in Sortase A reaction are shown in
Design of Trimers with Readthrough Codons
The development of clonal cell lines that highly express trimeric HIV-1 Envelope will facilitate manufacturing of high quality proteins for clinical and research purposes. However, it is challenging to identify the cells that express trimeric protein among the many cells making various forms of HIV-1 Envelope with in the cell population. To identify cells expressing trimeric HIV-1 Envelope protein, we designed an expression construct that simultaneously produces both secreted Envelope protein as well as membrane anchored Envelope protein. The secreted Envelope protein can be purified using standard methods and results in unaltered soluble envelope. The membrane-anchored Envelope protein serves to mark the cells within a population of cells that expresses trimeric Envelope. More specifically, the trimeric Envelope expressing cells are sorted by fluorescence-activated cell sorting using a HIV-1 trimer specific antibody. The sorted cells can then be used to initiate clonal populations of cells that have been phenotypically shown to express the protein of interest.
The expression construct is designed by taking advantage of the amber stop codon UAG in messenger RNA. The codon UAG usually signifies the end of the polypeptide sequence, but at a low rate the ribosome can readthrough this stop codon and continue to elongate the polypeptide chain. We incorporated this stop codon into our protein construct followed by the natural BG505 gp41 transmembrane and cytoplasmic tail sequence ended with two stop codons. Therefore, when the stop codon is readthrough a membrane-anchored gp120/gp41 heterodimer is formed. Loughran et al. (2014) identified that the efficiency of readthrough could be increased by flanking the amber stop codon with the nucleotides CTA. Readthrough could be even further augmented with the addition of CTAG nucleotides after the amber stop codon. We engineered expression constructs with both modifications to ensure an optimal ratio of membrane-anchored and secreted trimeric Envelope protein. Since the CTAG creates a shift in reading frame we added GC nucleotides after the CTAG motif to preserve the original reading frame. The addition of CTAGGC results in the membrane anchored protein having a leucine and glycine residue expressed before the transmembrane domain.
Germline B cell stimulation is a key initial step in the ability of HIV vaccines to elicit broadly neutralizing antibodies (bNAbs). Several bNAb lineages are known to target the CD4 binding site of HIV-1 envelope glycoprotein gp120, and these lineages are of particular interest for vaccines. Here we describe specific modifications of HIV-1 gp120 and gp140 to trigger germline activation and drive subsequent B cell maturation of CD4bs bNAbs. These modifications are two-fold: 1) site-specific mutagenesis of a glycine residue at position 458 of gp120, changing this residue to a tyrosine (G458Y mutation) and 2) biosynthesis of the G458Y mutated envelope glycoproteins in cells lacking the enzyme N-acetylglucosaminyltransferase, resulting in an enrichment of Man5 glycoforms of N-linked glycans that would otherwise be processed into complex-type glycans. Together these modifications permit the envelope glycoproteins of HIV-1 strain CH0505 to interact with germline forms of the CD4bs bNAb CH235.
We began these studies by testing the potency of CD4bs bNAbs and other HIV-1 bNAbs against viruses that were produced in either 293T or 293s/GnTI−/− cells. The latter cells were used to produce Man5-enriched glycoforms of pseudoviruses, with the rationale that a relatively small Man5 glycan would replace larger complex-type glycans that naturally exist and contribute to CD4bs masking. The oligosaccharide composition of HIV-1 Env consists mostly of under-processed high mannose (Man5-9 GlcNac2) glycans because steric constraints imposed by the highly glycosylated and trimeric structure Env impede the actions of α-mannosidases that are needed for complete processing (1-4). The smaller fraction of fully processed glycans exists mainly as sialylated bi-, tri- and tetra-antennary complex-type glycans (5-7), some of which border the CD4bs (5, 8). Importantly, nascent Env glycans that are trimmed by α-mannosidases and progress to complex-type glycans will remain as under-processed Man5 glycans in the absence of the enzyme UDP-N-acetylglucosamine:α-D-mannoside-β1,2-N-acetylglucosaminyltransferase (GnTI) (9), which is responsible for attachment of GlcNAc to Man5GlcNAc2 in the medial-Golgi as a requisite step for complete processing. HIV-1 Env proteins produced in 293s/GnTI−/− cells are known to be enriched for Man5 glycans, although as expected under-processed high mannose glycoforms (Man6-9) also exist (9, 10). There is at least one report of improved potency of mature CD4bs bNAbs against viruses produced in GnTI−/− cells (11).
Shown in
Despite the improved potency of many mature CD4bs bNAbs against Man5-enriched virus, germline-reverted forms of these bNAbs possessed no detectable neutralizing activity against either form of the virus (
We examined parental 426c and three variants of this virus containing a single mutation that removes the 276 glycan (426c.SM), a double mutation that removes 460 and 463 glycans (426c.DM), or a triple mutation that removes all three glycans (426c.TM). To preserve infectivity, the V1-V3 deletion that was introduced in the purified protein to facilitate exposure of the CD4bs remained intact in the Env-pseudotyped viruses. The neutralization phenotype of these viruses was extensively characterized with HIV-1 sera, a panel of mAbs that preferentially neutralize Tier 1 viruses, and a panel of bNAbs (Table 20, left columns). Loss of 1, 2 or 3 glycans had little or no effect on HIV-1 sera and did not render the virus sensitive to mAbs that preferentially neutralize Tier 1 viruses. Thus the glycan-deleted viruses maintained a Tier 2 phenotype. The viruses all resist neutralization by the MPER bNAb 2F5, the V2-glycan bNAbs CH01, PG9, PG16 and PGDM1400, the V3-glycan bNAbs PGT121 and PGT128, the glycan bNAb 2G12 and the CD4bs bNAbs HJ16 and b12. All four viruses were sensitive to the MPER bNAbs 4E10 and DH511.2_K3, the V3-glycan bNAb 10-1074 and the gp120/gp41 bNAbs PGT151 and VRC34.1, and these bNAbs were not affected by glycan deletion.
The only bNAbs clearly affected by glycan deletion were the CD4bs bNAbs VRC01, 3BNC117, VRC-CH31 and CH103 (boxed in red in Table 20). In particular, VRC01 and 3BNC117 were approximately 10-100 times more potent against 426c.TM than against the parental virus. Enhanced potency of 3BNC117 required all 3 glycans to be removed. VRC01 also required removal of all 3 glycans for maximum potency but unlike 3BNC117 it exhibited moderately enhanced potency seen against the single and double mutants. VRC-CH31 exhibited potent activity against the parental virus and double mutant but was inactive against the single and triple mutant, indicating a strict requirement for the presence of the N276 glycan. For CH103, modest neutralizing activity was seen against the double and triple mutant, while the parental and single mutant resisted neutralization at the highest concentration tested (40 μg/ml). All four viruses were resistant to CH235. Thus, overall the glycan-deleted variants of 426c provided little or no advantage for detecting CH103 and CH235 when produced in 293T cells.
Despite a nearly 100-fold improved potency of VRC01 against 426c.TM, we were unable to detect neutralization of this virus by germline-reverted VRC01. Part of the reason may due to the fact that the virus contains an intact V1-V3 region, whereas this region was deleted in the 426c.TM gp140 antigen that bound germline-reverted VRC01. Because V1-V3-deleted Env-pseudotyped viruses are non-infectious, we sought to determine whether Man5-enrichment would serve as an alternative strategy to further unmask the CD4bs on 426c.TM and enable detection of neutralizing activity by germline-reverted VRC01.
When parental 426c Env and the single, double and triple glycan-deleted variants of this Env were made as pseudoviruses in GnTI−/− cells and assayed in TZM-bl cells, all four viruses were infectious and maintained a Tier 2 neutralization phenotype (Table 20, columns on the right). Notably, they were also remarkably sensitive to neutralization by several CD4bs bNAbs (VRC01, 3BNC117, VRC-CH31 and CH103) compared to their 293T-grown counterparts (Table 20 and
We tested whether the 426c glycan mutants produced in GnTI−/− cells would permit detection of neutralization by a germline-reverted form of CD4bs bNAbs. As shown in
We tested near germline forms (mature HCDR3) of several additional VRC01-class bNAbs (VRC03, VRC04, VRC07, VRC18b, VRC20, VRC23 and VRC-CH31) and found that Man5-enriched 426c.TM permits detection of neutralization by near germline VRC07 (IC50=1.6 μg/ml) and VRC20 (IC50=4.6 μg/ml) (
We further showed that neutralization of Man5-enriched 426c.TM by near germline VRC01-class bNAbs is completely abolished when a VRC01 escape mutation (D279K) (16) is introduced (
While Man5-enriched glycoforms of glycan-deleted 426c Envs were useful for detecting near germline forms of VRC01-class bNAbs, they were not capable of detecting neutralization by germline and early intermediates of other CD4bs bNAb lineages, including CH103 and CH235. We investigated targeted glycan-deleted variants of the autologous transmitted/founder Env (CH0505TF) that evolved and gave rise to CH103 and its CH235 helper lineage (18, 19). As seen in Table 21, CH0505TF lacking four glycans at positions 197, 461/462, 276 and 362 (CH0505TF.gly4) demonstrated >1,000-fold enhanced sensitivity to early intermediates of the CH103 lineage compared to parental CH0505TF. Interestingly, Man5-enrichment showed only minor enhancement in sensitivity to these intermediates, with the exception of germline CH103 that was only detected with Man5-enriched CH0505TF.gly4. Intermediates of CH235 were detected at various levels with parental CH0505TF, CH0505TF.gly4 and CH0505TF.gly3.197 viruses, and this level of detection was much greater with Man5-enriched (GnTI−/−) versions of the viruses. No neutralization was detected with CH235 UCA.
We next sought to identify site-directed mutations that would allow us to map the epitopes of the activity detected with the CH103 and CH235 intermediates. Although these epitopes are well-characterized, the identification of diagnostic mutants would facilitate epitope mapping of polyclonal sera (e.g., vaccine sera) to determine whether positive neutralizing activity is related to these lineages. We began by testing the UCAs, intermediates and mature forms of CH235 for neutralizing activity against a G458Y mutant of CH0505TF. This mutation was chosen because it is a known escape mutation for VRC01-class bNAbs (20). CH0505TF was chosen because it was the only virus neutralized by early intermediate CH235_I4_v2_4A (Table 21). Surprisingly, rather than render the viruses less sensitive to neutralization, the presence of this mutation rendered the virus more susceptible to neutralization by the CH235 lineage, an effect that was more pronounced with Man5-enriched virus (Table 22). Even more remarkable, the combination of G458Y and Man5-enrichment now permitted detection of neutralization by three inferred UCAs of CH235 (Table 22,
Non-limiting example of additional possible mutations at position 458 are as follows:
G458F
G458W
G458M
G458Q
G458R (R is 2nd most frequent in LANL db)
G458K
G458H
G458N.
Without being bound by any specific theory, these mutations are expected to improve contacts like TYR at 458. These amino acid changes are selected based on size to increase potential contacts to I50 in CH235 UCA CDRH2.
Binding and/or affinity of antibodies to HIV-1 Env proteins G458Mut GnTI−/− cells produced, can be measured by any suitable method, for example but not limited to ELISA, SPR, and the like. See Example 1 and Example 8.
Any suitable GnTI−/− cell line could be use. See Bussow, K. in Current Opinion in Structural Biology 2015, 32:81-90; Chang et al. Structure. 2007 March; 15(3): 267-273. Glycosylation patterns of the envelopes produced in GnTI−/− cells could be determined by any suitable method.
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For CH235 UCA Nomenclature see Example 13. Sequences of Different CH235UCAs are Referenced in Example 8 and Shown in
Envelope Modifications that Permit Neutralization of HIV-1 by Germline-Reverted Forms of Broadly Neutralizing Antibodies to the CD4 Supersite
The ability to stimulate germline B cells that give rise to broadly neutralizing antibodies (bNAbs) is a major goal for HIV-1 vaccine development. BNAbs that target the CD4-binding site (CD4bs) of HIV-1 and exhibit extraordinary potency and breadth of neutralization are particularly attractive to elicit with vaccines. Glycans that border the CD4bs and impede the binding of germline-reverted forms of CD4bs bNAbs are potential barriers to naïve B cell receptor engagement. Targeted deletion of a subset of these glycans by sequon mutation has permitted binding but not neutralization, suggesting additional barriers exist. We produced HIV-1 in cells lacking the enzyme N-acetylglucosaminyltransferase (GnTI-) to enrich for Man5 glycoforms of N-linked glycans that would otherwise be processed into complex-type glycans. Our rationale was that small Man5 would replace larger complex-type glycans to further reduce steric barriers to germline CD4bs bNAb binding without disrupting native Env conformation. Targeted glycan-deleted HIV-1 produced in GnTI-cells was infectious and susceptible to potent neutralization by several germline-reverted VRC01-class bNAbs; neither glycan modification alone was sufficient for neutralization. Neutralization also was observed for germline-reverted and early intermediates of CH235/CH235.12 (VH1-46) and CH103 (VH4-59). Neutralization by germline-reverted CH235/CH235.12 required both Man5 enrichment and mutation of G458 in the V5 region of gp120 without targeted glycan deletion. These findings advance our understanding of the restrictions imposed by glycans in the elicitation of CD4bs bNAbs and provide a conceptual framework for improved vaccine designs.
Summary
Induction of broadly neutralizing antibodies (bNAbs) is a high priority for HIV-1 vaccines. Although these antibodies are made in HIV-1-infected individuals, it has not been possible to induce them with current vaccine immunogens. One reason for this is that the immunogens are not able to engage appropriate germline B cells to initiate the response. Here we show that glycans on the HIV-1 envelope can be modified in ways that should allow the envelope to stimulate germline B cells that give rise to a class of bNAbs targeting the CD4-binding site (CD4bs) of envelope gp120. These modifications involve the removal of select glycans, together with changes in the composition of other glycans, with the aim of exposing the CD4bs in a native conformation. An additional modification involves a glycine to tyrosine mutation (G458Y) in the CD4bs of gp120, which does not alter glycan composition. Inferred germline and early intermediates of certain CD4bs bNAbs exhibited neutralizing activity only when targeted glycan removal, or the G458Y mutation, was combined with an enrichment of Man5 glycoforms on HIV-1 Env-pseudotyped viruses. Our findings suggest that such modifications, and reverse-engineered versions of them, have potential to initiate and mature CD4bs bNAb responses.
Introduction
The CD4-binding site (CD4bs) of HIV-1 envelope glycoproteins (Env) is essential for virus entry [1] and is susceptible to some of the most potent broadly neutralizing antibodies (bNAbs) described to date, neutralizing up to 98% of circulating strains [2-10]. These bNAbs also prevent and SHIV infection in nonhuman primates [11-16] and produce transient reductions in plasma viremia in infected humans [17, 18] and macaques [19, 20]. Such features make CD4bs bNAbs highly attractive for vaccine development. Unfortunately, although the human immune system is clearly capable of making these antibodies in the setting of chronic infection, all efforts to elicit them with vaccines in non-human primates and humans have failed [21].
A major roadblock is the high levels of somatic hypermutation required to bind an epitope that is conformationally masked and sterically occluded by surrounding glycans [7, 9, 22, 23]. Mature CD4bs bNAbs resemble CD4 in their mode of binding and contact the CD4-binding loop while avoiding or accommodating potential clashes with loop D and the fifth variable (V5) regions of gp120, often contacting both of these latter regions [2, 22, 24]. Few immunoglobulin gene families appear to give rise to CD4bs bNAbs, most notably VH1-2 and the closely related VH1-46, both of which are utilized by the most potent CD4bs bNAbs (e.g., VRC01, 3BNC117, N6, CH235.12). Binding of these bNAbs is mediated by the heavy and light chains and is dominated by the heavy-chain second complementarity determining region (CDRH2) when either VH1-2 or VH1-46 are utilized [2, 5, 10]. Other CD4bs bNAbs (e.g., CH103, VRC13, VRC16 and HJ16) make use of multiple additional VH gene families, and their binding involves a CDRH3-dominated mode of recognition [6, 10].
Part of the reason why current immunogens fail to induce these bNAbs is that they do not bind germline-reverted forms of CD4bs bNAbs [7, 9, 22, 25-29] and therefore are unlikely to engage cognate naïve B cell receptors (BCRs). Weak germline binding has been detected against autologous Envs but it is not clear that this weak binding will provide an adequate stimulus to naïve B [30, 31].
Relationships between antibody structure and function are serving as a basis to reverse-engineer improved germline-targeting immunogens for the VRC01 class of CD4bs bNAbs. Notably, germline-reverted forms of these bNAbs are less positively charged [32] and their CDRH3 might play a more dominant role [33] than the mature bNAbs; both of these features could potentially influence interactions with complex-type glycans. Germline binding has been detected by introducing Env mutations that selectively remove glycans in the vicinity of the CD4bs that are predicted to clash with germline forms of the bNAbs. Targeted removal of three glycans from clade C strain 426c gp140ΔV1-V3, one at N276 in loop D that contacts the light chains of VRC01 and NIH45-46 [22, 34], and two at N460 and N463 in V5 that modulate VRC01 sensitivity [35], permit nanomolar affinity binding of germline-reverted forms of VRC01 and NIH45-46 [27]. These mutations also permit activation of B cells expressing germline-reverted BCRs of VRC01 and NIH45-46 in vitro [27], and they activate germline-reverted BCR of 3BNC60 in transgenic mice [36]. Deletion of glycan N276 is also one central design feature of engineered outer domain, germline-targeting (eOD-GT) immunogens that bind germline forms of the VRC01 class of bNAbs and activate germline-reverted BCR in knock-in mice [26, 37, 38].
HIV-1 Env is one of the most heavily glycosylated proteins known, with a glycan content that accounts for approximately 50% of its molecular mass [39]. A majority of these glycans exist as under-processed Man5-9GlcNac2 glycoforms owing to steric constrains imposed by the dense clustering of glycans and the trimerization of gp120-gp41 heterodimers that impede the actions of a-mannosidases required for complex glycan formation [40-43]. A predominance of high mannose glycans is seen with multiple forms of Env produced in different cell types [44-51], where a higher abundance of Man5GlcNac2 is present on virions and membrane associated Env than on recombinant gp120 and gp140 proteins [40, 44, 47]. The smaller proportion of fully processed glycans exists mainly as sialylated bi-, tri- and tetra-antennary complex-type glycans [4, 47, 52, 53], a portion of which surround the CD4bs [4, 54].
Complex-type glycans are arrested at Man5GlcNac2 in the absence of the enzyme N-acetylglucosaminyltransferase (GnTI) [55], which is responsible for attachment of GlcNAc to Man5GlcNAc2 in the medial-Golgi as a requisite step for complete processing. There is at least one report of improved neutralization potency of mature CD4bs bNAbs against Envs produced in GnTI-cells [56]. Here we converted complex-type glycans into smaller Man5GlcNac2 in the context of other Env modifications to reduce steric barriers to germline bNAbs without disrupting native Env conformation. We examined this by requiring neutralization of Env-pseudotyped viruses as proof germline bNAb engagement of native functional Env.
Results
Enhanced neutralization potency of mature CD4bs bNAbs against Envs produced in GnTI-cells
Multiple BNAbs were assessed for neutralizing activity against Env-pseudotyped viruses produced in either 293T or 293S GnTI-cells. The latter cells were used to generate Man5-enriched Env, with the rationale that relatively small Man5 would replace larger complex-type glycans that contribute to CD4bs masking. Initially, three mature CD4bs bNAbs (VRC01, 3BNC117 and VRC-CH31) were assayed against Envs from strains CE1176 and WITO. Greater potency (often >10-fold) was seen against GnTI-Envs for all three bNAbs (
Complementarity of Man5-enrichment and targeted glycan deletion for neutralization by mature CD4bs bNAbs
We next examined a combination of GnTI-production and targeted deletion of one or more glycans surrounding the CD4bs. Mutants of 426c Env were used that lacked glycan N276 (426c.SM), two glycans at N460 and N463 (426c.DM), or all three glycans (426c.TM) [27]. A fourth mutant, 426c.TM4, lacked all three glycans except that glycan N276 was removed by introducing S278R [36]. TM4 also contained a G471S mutation that facilitates germline bNAb binding to eOD-GT6 [26].
The glycan-deleted Envs, whether produced in 293T or GnTI-cells, maintained a tier 2 neutralization phenotype with HIV-1 sera and were mostly resistant to mAbs that preferentially neutralize Tier 1 Envs (non-neutralizing Abs) (Table 24). Envs produced in GnTI-cells were more sensitive to HIV-1 sera than their 293T-grown counterpart, especially the TM and TM4 mutants, but still within the Tier 2 spectrum.
As reported previously for NIH45-46 [27], glycan deletion increased the susceptibility of 426c Env to neutralization by mature CD4bs bNAbs when the virus was produced 293T cells (Table 24,
GnTI-production enhanced the susceptibility of parental 426c Env to neutralization by mature VRC01, 3BNC117, VRC-CH31 and CH103 compared to when the Env was produced in 293T cells, and this susceptibility was further enhanced against one or more glycan-deleted variants of 426c Env, demonstrating the complementary nature of glycan deletion and GnTI-production for these mature bNAbs (
Neutralization by germline-reverted forms of VRC01-class bNAbs requires a combination of Man5-enrichment and targeted glycan deletion
Germline-reverted and early intermediates of CD4bs bNAbs were evaluated for an ability to neutralize GnTI-version of targeted glycan deleted 426c Envs. These tests included near-germline forms of several VRC01-class bnAbs, which possess a mature HCDR3 region for which the germline form could not be inferred with existing sequences. They also included fully reverted germline forms of VRC-CH31, CH103 and CH235/CH235.12. Mature CH235 and CH235.12 are members of the same lineage and exhibit 18% and 90% neutralization breadth, respectively, against a multiclade panel of 199 viruses [2]. Their unmutated common ancestor (UCA) is referred to here as CH235 UCA2.
GnTI-versions of the 426c SM, TM and TM4 Envs were remarkably sensitive to neutralization by germline-reverted VRC01, with IC50s of 0.99, 2.5 and 0.44 μg/ml, respectively (
Germline forms of other VRC01-class bNAbs also neutralized GnTI-versions of the TM and TM4 Envs (
Attempts were made to detect neutralization by germline reverted and intermediates of the VRC01-like bNAb, VRC-CH31. Here, 426c.DM was used because the absence of glycan N276 in the single and triple glycan mutant Envs renders 426c resistant to mature VRC-CH31 (
Neutralization by Germline-Reverted CH103 and Intermediates of CH103 and CH235
The lack of susceptibility of Man5-enriched versions of glycan-deleted 426c Envs to neutralization by germline-reverted and intermediates of CH103 and CH235 (Table 24) led us to test glycan-deleted variants of the autologous transmitted/founder Env (CH0505TF) that evolved and gave rise to CH103 and its CH235-helper lineage [6, 30]. One CH0505TF mutant lacked four glycans at N197, N461/462, N276 and N362 (gly4), whereas the others lacked three glycans by adding back glycans N197 (gly3.197), N276 (gly3.276) or N461 (gly3.461) [62]. CH0505TF naturally lacks glycan N362.
As reported previously [62], 293T versions of parental CH0505TF and all four glycan mutants were sensitive to mature CH103, CH235 and CH235.12, with the gly4, gly3.276 and gly3.461 Envs often being 10-1000 times more sensitive than the parental and gly3.197 Envs (
Notably, GnTI-versions of the gly4 and gly3.461 Envs were moderately sensitive to neutralization by germline-reverted CH103 (IC50=6.4 and 10.2 μg/ml, respectively), whereas 293T versions of these Envs were not neutralized (
Neutralization by CH235 UCA2 Requires a Combination of Man5-Enrichment and Mutation of G458 in gp120
We were interested in developing diagnostic mutants to map the neutralizing activity detected with intermediates of the CH103 and CH235 lineages. Two known CD4bs bNAb resistance mutations, N280D (loop D) and G458Y (V5 proximal), were introduced into CH0505TF and assayed as 293T-produced Envs against a panel of mature bNAbs (Table 23). N280D and G458Y were strong resistance mutations for VRC01 and 3BNC117. N280D was a strong resistance mutation for CH235, N6 and VRC-CH31. Neither mutation had a strong impact on CH103, although a 3-fold reduction in neutralization was seen with G458Y. To design a better resistance mutation for CH103, additional point mutations were investigated that in crystal structures are contacts for CH103 but not CD4 (to maintain infectivity). Three mutations in V5 (N461A, N462A and T463A) had no effect but a fourth mutation in the CD4-binding loop (S365P) conferred resistance to CH103 (Table 23). The S365P mutation also conferred partial resistance to VRC-CH31 (Table 23). No mutation reduced the neutralizing activity of CH235.12.
The N280D, G458Y and S365P mutants of CH0505TF were used as GnTI-Envs for mapping (Table 23 and Table 25). S365P was an effective resistance mutation for CH103 intermediates but was only modestly effective for mature CH103. G458Y conferred partial resistance to CH103 intermediates (more complete resistance was seen with the 293T version of this mutant Env, Table 25). N280D was an effective resistance mutation for the one intermediate and two mature forms of CH235 that neutralized the parent virus.
Surprisingly, the G458Y mutation in the context of CH0505TF Env produced in GnTI-cells conferred a high level of susceptibility to neutralization by CH235 UCA2 and all intermediates of this lineage (
Additional amino acid substitutions at position 458 were tested for an effect similar to tyrosine. CH0505TF Env was sensitive to neutralization by CH235 UCA2 when position 458 was occupied by phenylalanine (F), tryptophan (W), arginine (R), cysteine (C) and leucine (L), although tyrosine remained superior (
To gain insight into the G458Y impact on CH235 UCA2, the crystal structure of gp120 in complex with CH235 [2] was examined. As shown in
We asked whether CH0505TF.G458Y GnTI-Env existed in a more open trimer conformation that is associated with a highly sensitive Tier 1 neutralization phenotype [68-70]. The GnTI-version of CH0505TF.G458Y Env was only 3 times more sensitive to HIV-1 sera than the parental Env grown in either GnTI- or 293T cells (Table 25). It was also resistant to a panel of antibodies that show preference for Tier 1 Envs (non-neutralizing Abs in Table 25). Moreover, the GnTI-version of a highly neutralization sensitive Tier 1 variant of CH0505TF Env (CH0505.w4.3) was not neutralized by CH235 UCA2, and was not more sensitive to the intermediates and mature forms of CH235 compared to the GnTI-version of parental CH0505TF Env (Table 25). Overall, the structural determinants that permit neutralization of Man5-enriched CH0505TF.G458Y Env by CH235 UCA2 may be less subtle than the open trimer conformation that leads to a Tier 1 neutralization phenotype.
Discussion
Part of the reason why current vaccine immunogens fail to induce bNAbs is that they are unable to stimulate appropriate germline-encoded B cell receptors. To overcome this limitation, researchers are identifying natural and engineered Env proteins that bind germline-reverted forms of the bNAbs as partial mimics of the naïve B cell receptors [6, 26, 27, 36-38]; such proteins are in early stages of development and it is unclear whether they will initiate correct antibody lineages in humans and wild-type animal models. We sought Env modifications that would permit neutralization by germline forms of CD4bs bNAbs as stringent proof of native envelope engagement by the antibodies. One previous report described weak neutralization by germline-reverted CH103 against an early autologous Tier 1 Env [30], which was also observed here (IC50=24 μg/ml, Table 25). Another report described neutralization of 426c.SM and TM by VRC01-class bNAb NIH45-46 but only at high antibody concentrations (IC50˜100 μg/ml) [27]. We describe Env modifications that permit far greater neutralization potency by germline forms of several CD4bs bNAbs, including VRC01-class (VH1-2) (IC50=0.03 μg/ml), CH235/CH235.12 (VH1-46) (IC50=0.16 μg/ml), and to a lesser extent CH103 (VH4-59) (IC50=6.4 μg/ml). This was accomplished by using either targeted glycan deletion or mutation of gp120 position 458, combined with Man5-enrichment of N-linked glycans that would otherwise be fully processed into complex-type glycans.
Man5-enrichment in GnTI-cells was hypothesized to reduce steric barriers to germline bNAb binding without disrupting native Env conformation. That Man5-enriched Envs were infectious is consistent with previous reports [45, 54] and indicates that native conformation was indeed preserved. Several mature CD4bs bNAbs were more potent against Man5-enriched Envs than wild type Envs, while most bNAbs to epitopes outside the CD4bs were not affected (Tables 24 and 25). One exception is PGT151 (gp120-gp41 epitope), which was negatively impacted by Man5-enrichment. This agrees with previous indications that PGT151 requires one or more complex-type glycans [58, 59]. Another exception was the increased potency of V2-apex bNAbs CH01 and PG9 against glycan-deleted, Man5-enriched variants of CH0505TF (Table 25). Further studies are warranted to determine whether Man5-enrichment might be a viable approach to initiate V2-apex bNAbs.
It was necessary to couple Man5-enrichment with targeted glycan deletion in 426c Env to achieve neutralization by germline-reverted forms of VRC01-class bNAbs. A simple explanation for why both modifications were necessary is that not all complex-type glycans acting as steric barriers to germline binding were removed by targeted deletion. Indeed, the lower glycan density created by targeted sequon removal has potential to relieve steric constraints on a-mannosidases and result in an increased number of fully processed complex-type glycans [40-43]. Any additional complex-type glycans generated in this way should remain arrested as smaller ManS glycoforms when produced in GnTI-cells, thereby affording a lower barrier to germline binding.
A remarkable finding was that mutation of G458 in the V5 region of gp120 (a CD4 contact residue) enabled germline-reverted and several intermediates of CH235/CH235.12 to potently neutralize Man5-enriched CH0505TF Env. Y458 was most effective but other amino acids also permitted neutralization. Mutation of this site, usually to negatively charged aspartic acid (G458D), confers resistance to certain VRC01-class bNAbs [61, 63-67] and was shown here as a G458Y mutation to confer resistance to VRC01 and 3BNC117. Neutralization by germline-reverted and early intermediates of CH235/CH235.12 required both Man5-enrichment and mutation of G458 without the need for targeted glycan deletion. At the molecular level, G458Y mutation restores a potential contact site in the CDRH2 region of germline-reverted CH235/CH235.12 that is lost when a tryptophan (W50) in the mature CDRH2 is reverted to isoleucine in the UCA. Since G458 is highly conserved (>95%) among circulating group M Env sequences [61], and was present in all viral sequences examined from the CH235/CH235.12 donor [30], it seems unlikely that Y458 (or another substitution at this site) contributed to the natural response that gave rise to CH235/CH235.12 in this individual. Indeed, the rarity of non-G at this position may be part of an evasion mechanism to disfavor the production of CH235/CH235.12-like bNAbs. Nonetheless, Man5-enriched CH0505TF.G458Y Env with all sequons intact may be a potent stimulator of germline CH235/CH235.12-like antibodies, and it remains possible that such variants exited in the donor at a low frequency that went undetected. Similarly, heterogeneity in Env sequon location and occupation, and in the composition of glycans at occupied sites [49, 51, 52] make it possible that other CD4bs bNAb responses in HIV-1 infected individuals are driven in part by a subpopulation of Envs that are both Man5-enriched and lack key sequons.
The Env modifications reported here suggest new avenues to pursue for immunogen design. For example, immunogens could be tailored to initiate the CH235/CH235.12 lineage by priming with Man5-enriched CH0505TF.Y458 Env protein produced in GnTI-cells and boosting with reverse engineered immunogens that contain G458 and a full complement of complex-type glycans. It will also be of interest to investigate existing VRC01 germline-targeting immunogens, such as 426c core [27, 36] and eOD-GT8 [38], that are produced in GnTI-cells. Success may depend on combining these modifications with other design features, such as closely mimicking native Env structure to assure correct angle of antibody approach [71], and circumventing immunologic tolerance [72]. Notably, it has not been possible to accurately infer the germline version of the CDRH3 region of VRC01-class bNAbs with existing sequences. Thus, while detection of neutralizing activity by the germline form of VRC01 used here is encouraging, additional Env modifications might be needed to adequately engage true VRC01-class germline B cells.
The modified Envs described here have additional value by enabling detection of early precursors of CD4bs bNAbs induced by candidate immunogens. Detection would be based on functional neutralizing activity in a high throughput assay and would complement other technologies, such as antigen-specific memory B cell sorting and immunoglobulin sequence analyses. Until the technology is refined to capture a wider range of CD4bs bNAb precursors, negative neutralizing activity would not necessarily mean that precursors are absent. Additional efforts are needed to be more inclusive of the full range of CD4bs bNAbs and to enable detection of early precursors of bNAbs to other epitopes in neutralization assays. The insights provided here should facilitate these efforts as they relate to both immune monitoring and immunogen design.
Methods
Cells
TZM-bl, 293T/17 and 293S/GnTI-cells were maintained in Dulbecco's Modified Eagle's Medium (DMEM) containing 10% fetal bovine serum (FBS) and gentamicin (50 μg/ml) in vented T-75 culture flasks (Corning-Costar). Cultures were incubated at 37° C. in a humidified 5% CO2-95% air environment. Cell monolayers were split 1:10 at confluence by treatment with 0.25% trypsin, 1 mM EDTA.
Antibodies and HIV-1 Sera
The monoclonal antibodies used in this study have been previously described: CD4bs bNAbs VRC01, VRC03, VRC04, VRC07, VRC-18b, VRC20, VRC23, 12A12 [8-10, 24], 3BNC117, 3BNC60 [7], VRC-CH31 [73], N6 [5], HJ16 [3] and IgG1b12 [74]; high mannose glycan-specific bNAb 2G12 [75]; gp41 membrane proximal external region (MPER)-specific bNAbs 2F5, 4E10 [76], 10E8 [77] and DH511.2_K3 [78]; V2-apex bNAbs PG9, PG16 [79], CH01 [73] and PGDM1400 [80]; V3-glycan bNAbs PGT121, PGT128 and 10-1074 [56, 81]; gp41-gp120 interface bNAbs PGT151 [58] and VRC34.01 [60]. VRC01, VRC34.01 and 10E8 were produced by the Vaccine Research Center, NIH. N6 was obtained from Dr. Mark Connors. 3BNC117, 3BNC60 and 10-1074 were obtained from Dr. Michel Nussenzweig. VRC-CH31 and CH01 were produced by Catalent Biologics (Madison, Wis.). DH511.2_K3 was produced by the Human Vaccine Institute, Duke University Medical Center. HJ16 was obtained from Dr. Davide Corti. IgG1b12, 2G12, 2F5, 4E10, PG9 and PG16 were purchased from Polymun Scientific (Klosterneuburg, Austria). PGDM1400, PGT121, PGT128 and PGT151 were a kind gift from Dr. Dennis Burton.
In addition to these mature bNAbs we utilized UCAs, intermediates and mature forms of CH103, CH235/CH235.12 [2, 30] and VRC-CH31 [10], which were produced by the Human Vaccine Institute, Duke University Medical Center, Durham, N.C. The unmutated common ancestor (UCA) sequence for the CH235/CH235.12 lineage used in this study differs by one amino acid from the UCA described previously [2]. The UCA used here, which we refer to as CH235 UCA2, has a methionine in the 4th position of the light chain in place of a leucine in the previously described UCA version. Other antibodies included germline-reverted forms of the VRC01-class bNAbs VRC01, VRC03, VRC04, VRC07, VRC18b, VRC20, VRC23, 12A12 and 3BNC117 [9, 10, 24, 27], which were produced at the Vaccine Research Center, NIH. These latter germline-reverted antibodies possess a mature HCDR3 region, which could not be inferred with existing sequences.
Neutralization Tier phenotyping was performed with serum pools from individuals in southern Africa (South Africa, Malawi and Tanzania) who participated in a CHAVI study of chronic HIV-1 infection (CHAVI samples 0406, 0060, 0642, 0293, 0598, 0537, 0468, 0461, 0382 and 0134). These study subjects had all been infected for at least three years. Samples from 6-10 time points collected over 8-60 months were pooled on a per-subject basis and heat-inactivated for 30 minutes at 56° C. For deeper interrogation of neutralization phenotype, a set of monoclonal antibodies was used that show a strong preference for Tier 1 viruses. This set included V3-specific antibodies 2219, 2557, 3074, 3869, 447-52D and 838-D, and the CD4bs antibodies 654-30D, 1008-30D, 1570D, 729-30D and F105, all produced by Drs. Susan Zolla-Pazner and Miroslaw K. Gorny at New York University and the Veterans Affairs Medical Center, New York, N.Y.
Pseudotyping Envs
Full-length functional HIV-1 Envs were used for virus pseudotyping. Previous reports described Envs for strains CE1176 [82], WITO [83], TRO.11 [83], CH0505TF and CH0505.w4.3 [2]. Glycan deleted Envs CH0505TF.gly4, CH0505TF.gly197, CH0505TF.gly3.276 and CH0505TF.gly3.461 were described by Zhou et al. [62]. Envs for 426c and the glycan deleted variants 426c.SM, 426c.DM and 426c.TM were described by McGuire et al. [27]. In some cases N280D, G458Y and S365P mutations were introduced by site-directed mutagenesis as described [84].
Transfection
Env-pseudotyped viruses were produced in either 293T/17 or 293S GnTI-cells (American Type Culture Collection) as described [85]. 293S GnTI-cells lack the enzyme N-acetylglucosaminyltransferase and have been shown to yield HIV-1 Envs that contain Man6-9 glycoforms and are enriched for under-processed Man5 glycoforms in place of complex glycans [45, 54]. Env-pseudoviruses were generated by transfecting exponentially dividing 293T/17 or 293 S/GnTI-cells (5×106 cells in 12 ml growth medium in a T-75 culture flask) with 4 μg of rev/env expression plasmid and 8 μg of an env-deficient HIV-1 backbone vector (pSG3ΔEnv), using Fugene 6 transfection reagent. Cells were washed after 3-8 hours and incubated in fresh growth medium without transfection reagents. Pseudovirus-containing culture supernatants were harvested 2 days after transfection, filtered (0.45 μm), and stored at −80° C. in 1 ml aliquots. Infectivity was quantified in TZM-bl cells by performing serial fivefold dilutions of pseudovirus in quadruplicate wells in 96-well culture plates in a total volume of 100 μl of growth medium for a total of 11 dilution steps. Freshly trypsinized cells (10,000 cells in 100 μl of growth medium containing 75 μg/ml DEAE-dextran) were added to each well, and the plates were incubated at 37° C. in a humidified 5% CO2-95% air environment. After a 48-hour incubation, 100 μl of culture medium was removed from each well and 100 μl of Britelite reagent was added to the cells. After a 2-min incubation at room temperature to allow cell lysis, 150 μl of cell lysate was transferred to 96-well black solid plates (Corning-Costar) for measurements of luminescence using a Victor 3 luminometer (Perkin-Elmer Life Sciences, Shelton, Conn.). A dilution of virus that results in 50,000-250,000 relative luminescence units (RLUs) was used for neutralization assays.
Neutralization Assay
Neutralization assays were performed in TZM-bl cells (NIH AIDS Research and Reference Reagent Program) as described [85]. Briefly, a pre-titrated dose of Env-pseudotyped virus was incubated with serial 3-fold dilutions of test sample in duplicate in a total volume of 150 μl for 1 hr at 37° C. in 96-well flat-bottom culture plates. Freshly trypsinized cells (10,000 cells in 100 μl of growth medium containing 20 μg/ml DEAE dextran) were added to each well. One set of control wells received cells+virus (virus control) and another set received cells only (background control). After 48 hours of incubation, the cells were lysed by the addition of Britelite (PerkinElmer Life Sciences) and three quarters of the cell lysate was transferred to a 96-well black solid plate (Costar) for measurement of luminescence. Neutralization titers are either the serum dilution (ID50) or antibody concentration (IC50) at which relative luminescence units (RLU) were reduced by 50% compared to virus control wells after subtraction of background RLUs.
Structural Modeling and Analysis
Structural modeling of mutations in the CH235 gp120 complex (PDB: 5F9W) [2] was performed with the PyMOL Molecular Graphics System, Version 1.8 Schrödinger, LLC (http://www.pymol.org) using the mutagenesis wizard and placing mutated residues in the rotamer state corresponding to the minimum strain value. Hydrophobicity scores were assigned to amino acids using the Wimley-White whole-residue octanol scale [86]. For position 458 mutants that had neutralization curves that did not reach 50% neutralization at the highest concentration (10 mg/ml), the IC50 value was set to 25 for the regression analysis.
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>50
>25
>25
>25
>25
>25
>17
>25
1.2
0.16
0.08
0.03
<0.02
<0.02
<0.02
1Highlight values in the top section of the table are the most dramatic cases of resistance-mediating effects.
2Highlighted values in the bottom section of the table are the remarkable neutralization potencies seen with UCAs and intermediates of CH235.
0.37
0.07
0.016
0.005
0.064
<0.005
<0.005
<0.005
1GMT, geometric mean titer of polyclonal sera
Several CH235UCAs were deduced, made and used in experiments throughout this application.
Table 28 shows a summary of the different CH235UCAs. Sequences are referenced in Examples 8 and 11, and shown in
In some experiments, e.g. experiments depicted in Examples 10 and 11 CH235 UCA forms were recombinantly expressed and purified without size exclusion chromatography step.
Some experiments in Example 13 compared the properties of the SEC-purified antibody and non-SEC purified CH235UCAtkLL_v3 antibody. In some embodiments, the SEC purification affects binding and neutralization properties. For example, SEC purified CH235UCA antibody shows reduced neutralization and binding, whether or not the viruses are produced in GnTI−/− cells. See
Experiments in Example 13 are conducted with SEC purified antibody unless noted otherwise. In some of the figures, and in Examples 13 the size exclusion chromatography purified antibody is referred to as purified antibody.
Germline-Targeting and Reverse Engineering to Elicit CH235.12 Lineage BNAbs
This example provides some strategies and non-limiting embodiments of immunogens to induce broad neutralizing antibodies, including CH235 lineage of antibodies.
The ability to stimulate germline B cells that give rise to broadly neutralizing antibodies (bNAbs) is a major goal for HIV-1 vaccine development. bNAbs that target the CD4-binding site (CD4bs) and exhibit extraordinary potency and breadth of neutralization are particularly attractive to elicit with vaccines. Glycans that border the CD4bs and impede the binding of germline-reverted forms of CD4bs bNAbs are potential barriers to naïve B-cell receptor engagement. We used pseudovirus neutralization as a means to identify Env modifications that permit native Env trimer binding to germline reverted CD4bs bNAb CH235.12 (VH1-46). Two mutations (N279K.G458Y), when combined with Man5-enrichment of N-linked glycans that are otherwise processed into complex glycans, rendered autologous CH0505TF Env highly sensitive to neutralization by CH235.12 UCA. These findings suggest a vaccine
Example 8 described a bnAb, CH235.12, which has ˜90% breadth, and uses VH1-46 chain. The deduced UCA for this lineages, CH235UCA does not neutralize wild type virus. Without bound by specific theory, virus modifications that permit neutralization would be candidate germline-targeting immunogens. This information also suggests reverse-engineering strategies to mature the response.
In some aspects, the goal was to identify Env modifications that permit neutralization by germline-reverted CD4bs bNAbs. In some embodiments, the hypothesis was that conversion of bulky complex-type glycans to smaller Man5GlcNac2 glycoforms will reduce steric barriers to germline BNAb binding without disrupting native Env conformation.
Previous work has explored glycan modifications and has shown that deletion of a subset of glycans surrounding the CD4bs is a feature that has permitted binding and BCR activation by germline-reverted forms of VRC01-class BNAbs. See McGuire et al., J Exp Med, 210:655-663, 2013; McGuire et al., Nat Comm 7:10618, 2016; Jardine et al., Science 340, 711-716, 2013; Jardine et al., Science 349, 156-161, 2015; Jardine et al., Science 351, 1458-1463, 2016.
See also Zhou, T. et al. Cell Reports 19:719-732, 2017 where inter alia CH0505TF; CH0505TF.gly4 (deleted N197, N276, N461, naturally lacks N362); CH0505TF.gly3.197; CH0505TF.gly3.276; CH0505TF.gly3.461 were studied. Man5-enriched versions of these viruses were not neutralized by CH235UCA. Man5-enriched CH0505TF was highly sensitive to CH235 intermediates. Glycan deletion did not improve neutralization by CH235 intermediates
Induction of VH1-46 utilizing CD4 binding site (CD4bs) ANC131, CH235-class broadly reactive neutralizing antibodies (bnAbs) is desirable because the affinity matured antibodies of this class are quite broad and potent, are not autoreactive, nor have long HCDR3 regions, and, in the case of CH235, do not have difficult to induce insertions or deletions that need to occur en route to bnAb breadth (Cell 165: 449-463, 2016). However, there are only a few of these bnAbs described and only one bnAb lineage isolated from the time of acute infection to bnAb breadth, CH235 lineage (Cell 165: 449-463, 2016). Moreover, Envs that bind to the CH235 UCA at high affinity have not been available. Here, we show that deletion of certain glycans and inclusion of a G458Y mutation creates a CH505 M5 Envelope from a low affinity binding Env to a high affinity binding Env for the CH235 UCA.
Effect of Affinity of Immunizing Antigens on Induction of Germinal Center (GC) Responses
The affinity of stimulating antigens has a profound effect on the outcome of the germinal center response. High affinity antigens can prevent a B cell from staying in the germinal center, and promote rapid maturation of a B cell to a short-lived plasma cell (Journal of Exp. Med. 203: 1081, 2006). Recent data suggest that affinities from high microM to low nM can activate bnAb precursors, but the key is what the affinity of sequential Env immunogens must be to retain stimulated bnAb B cell lineages in the germinal center. To this end, we have selected and produced at the Duke Human Vaccine Institute (DHVI) CGMP facility the M5 gp120 that has an apparent affinity for the CH235 UCA of 4.6 microM while the mature CH235 bnAb has an affinity of 8.0 nM for the M5 gp120 Env (
For additional immunization strategies see also
Design of the CH505 M5 G458Y Stabilized SOSIP Trimer that Targets the CH235 UCA at Various Affinity
To design an additional “high affinity” immunogen capable of binding to the CH235 UCA at nM affinity, mutations that might increase binding of the CH235 UCA to Env based on the CH235-Env co-crystal structure (Cell 165: 449-463, 2016) were studied. The CH505 M5 Env expressed as a stabilized (4.1) SOSIP trimer bound to the CH235 UCA with an apparent Kd of 231 nM (
Non-limiting examples of neutralization of envelopes comprising G458Mut are shown in
Non-limiting examples of neutralization of envelopes comprising amino acids other than lysine (K) at Env position 279 are shown in
Multimerization of CH505 M5 G458Y Env
It remains to be determined if multimerization of Env immunogens will be required for optimal immunogenicity. Multimerization strategies are more complicated and purification of trimer multimers will require considerable pre-production work. We have developed methods for expressing and purifying the CH505 M5 G458Y Env.
Any of the immunogens of the invention could be tested for Ca2+ flux in a suitable cell line comprising a desired antibody, e.g. but not limited to CH235UCA2.
Animal Studies
The immunogens of the invention could be studied in various animal models. In some embodiments, the immunogenicity will be studied in an animal model comprising CH235UCA VH and/or VL chains knocked into an animal, e.g. a mouse. Any suitable animal could be used including rabbits, mice, and non-human primates.
In one example, CH235UCA knock in mice are immunized as follows:
Group 1: CH505 M5 SOSIPsG458Y grown in GnTI−/− cells (×4)×5 mice
Group 2: M5 gp120delta8 (×4)×4 mice
Adjuvant for both groups is GLA-SE. The immunogenicity in these animals will be analyzed by any suitable assay including neutralization, ELISA, etc.
Animal studies wherein the immunogens of the invention are administered as mRNA, for example but not limited as modified mRNAs formulated in LNPs, or self-replicating mRNAs formulated in LNPs.
Table 29 shows a summary of the sequence Evolution of CH235 Lineage: SHM, Timing, and Conformity of CH235-Lineage Development from UCA to Antibody with 90% Breadth. VH-gene mutability accounts for the majority of positional conformity of CH235 lineage. (SEQ ID NOS 314-323, respectively). SEQ ID NOS 314-323 are included in the Sequence Listing which is submitted electronically herewith in ASCII format and is hereby incorporated by reference in its entirety and forms part of the specification. See also FIG. 43C of U.S. Provisional Application No. 62/511,226 filed May 25, 2017 and U.S. Provisional Application No. 62/565,952 filed Sep. 29, 2017.
Table 30 shows a summary of CH235 Lineage: Sequences and Neutralization Fingerprint Dendrogram. Sequences (SEQ ID NOS 324-385, respectively) and antibodies isolated from 17 time points from 6 to 323 weeks post-transmission and comparison of mutation patterns to other IGHV1-46 (1B2530 and 8ANC131) and IGHV1-2 (VRC01, VRC-CH31 and VRC-PG04) derived broadly neutralizing antibodies. IGHV1-46*01 is used as reference for IGHV1-46 derived antibodies and IGHV1-2*02 is used as reference for the three VRC01-class antibodies. SEQ ID NOS 324-385 are included in the Sequence Listing which is submitted electronically herewith in ASCII format and is hereby incorporated by reference in its entirety and forms part of the specification. See also FIG. 48A of U.S. Provisional Application No. 62/511,226 filed May 25, 2017 and U.S. Provisional Application No. 62/565,952 filed Sep. 29, 2017.
Table 31 shows a summary of sequence Similarity Between VH1-2 and VH1-46 Broadly Neutralizing Antibodies and Mutability of Germline Genes. Amino acid alignment of 8ANC131 (SEQ ID NO: 387) and CH235 (SEQ ID NO: 388) to the IGHV1-46 (SEQ ID NO: 386) germline gene was performed. SEQ ID NOS 386-388 are included in the Sequence Listing which is submitted electronically herewith in ASCII format and is hereby incorporated by reference in its entirety and forms part of the specification. See also FIG. 50A of U.S. Provisional Application No. 62/511,226 filed May 25, 2017 and U.S. Provisional Application No. 62/565,952 filed Sep. 29, 2017.
Table 32 shows a summary of sequence probability distribution of the number of sharing mutation positions for each pair of antibodies (SEQ ID NOS 389-395, respectively, in order of appearance). SEQ ID NOS 389-395 are included in the Sequence Listing which is submitted electronically herewith in ASCII format and is hereby incorporated by reference in its entirety and forms part of the specification. See also FIG. 50B of U.S. Provisional Application No. 62/511,226 filed May 25, 2017 and U.S. Provisional Application No. 62/565,952 filed Sep. 29, 2017.
Table 33 shows primers designed with the online Agilent Quikchange primer designer tool (www.thermofisher.com) (SEQ ID NOS 8-15, respectively, in order of appearance).
Table 34 shows designed PCR primers. PCR amplifications performed with a common 5′ primer II A (Clontech) and an Ig gene specific 3′ primer (SEQ ID NO: 16) using KAPA HIFI qPCR kit (Kapa Biosystems). PCR amplification performed with primers with 454 sequencing adapters
This application claims the benefit of and priority to U.S. Provisional Application No. 62/511,226 filed May 25, 2017 and U.S. Provisional Application No. 62/565952 filed Sep. 29, 2017, the contents of each of which are hereby incorporated by reference in their entireties.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2018/034772 | 5/25/2018 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 62511226 | May 2017 | US | |
| 62565952 | Sep 2017 | US |
