Patent Application
20230181717
HIV-1 envelope glycoprotein (Env) is the sole target for neutralizing antibodies (NAbs) during natural infection. Like other class-I viral fusion proteins, HIV-1 Env is a homotrimer of gp120-gp41 heterodimers. Before infection, the trimeric Env proteins on HIV-1 virions are in the prefusion state, which is intrinsically unstable (or termed metastable) in order to undergo a rapid conformational change to mediate cell entry. In a small fraction (5-15%) of HIV-1 patients, some NAbs generated during early infection can co-evolve with viruses and become broadly neutralizing antibodies (bNAbs) over an extended period of time (e.g., more than ten years). So far, panels of bNAbs have been isolated from elite HIV-1 patients, suggesting that protective HIV-1 vaccines may be achieved by eliciting such bNAbs during immunization. Significant progresses in Env stabilization have been made in rational HIV-1 vaccine design in the recent years. Various design strategies were proposed to stabilize HIV-1 Env in “native-like” prefusion trimer structures (Ward & Wilson, Immunol Rev 2017, 275(1):21-32; Sanders & Moore, Immunol Rev 2017, 275(1):161-182). Notably, one strategy based on the analysis of Env metastability proved to be highly effective and provided a general solution to Env-based HIV-1 vaccine design. First, an HR1 bend (aa 547-569) in the gp41 ectodomain (gp41ECTO) was identified as the primary cause of HIV-1 Env metastability (Kong et al., Nat. Commun. 2016, 7:12040). An uncleaved, prefusion-optimized (UFO) design was developed to stabilize HIV-1 Env trimers by combining a redesigned HR1 bend and a GS linker at the furin cleavage site. The UFO design has been applied to diverse HIV-1 Envs with great success, producing soluble trimers with significantly higher yield, purity, and stability than the SOSIP and NFL designs. It was also demonstrated that gp41ECTO is the sole source of metastability and BG505 gp41ECTO of the UFO design (termed UFO-BG) can be used to stabilize diverse HIV-1 Envs with substantial trimer yield, purity, and stability (He et al., Sci Adv 2018, 4: aau6769). The UFO and UFO-BG designs thus provide a simple, general, and effective strategy for Env stabilization and trimer-based HIV-1 vaccine design.
It is well known that single-subunit vaccines are less effective than virus-like particles (VLPs), which induce strong immune responses due to their large size and dense antigen display. VLPs have shown exceptional success as human vaccines, as exemplified by vaccines developed for human papillomaviruses (HPV), hepatitis B virus (HBV), and hepatitis E virus (HEV). Self-assembling protein nanoparticles (SApNPs) have been considered an alternative for developing VLP vaccines without involving complicated purification methods typically required for VLPs. Development of SApNP vaccines for HIV-1 and other viral pathogens have been reported. These include, e.g., display of trimeric HIV-1 antigens such as V1V2, gp120, and gp140 on 24-meric ferritin and 60-meric E2p (He et al., Nat. Commun. 2016, 7:12041), and display of UFO and UFO-BG trimers of diverse HIV-1 Envs on 24-meric ferritin and 60-meric I3-01 (He et al., Sci Adv 2018, 4:aau6769).
Despite the substantial progresses in vaccine design, major issues remain to be addressed in the development of potent and effective HIV-1 vaccines, e.g., low immunogenicity and sporadic tier 2 neutralizing antibody responses. The present invention are intended to address these and other unmet needs in the art.
In one aspect, the invention provides methods for enhancing immunogenicity of HIV-1 nanoparticle vaccines. The methods involve (a) contacting an HIV-1 nanoparticle vaccine with an enzyme that is capable of removing or shortening the N-linked glycan chain from the vaccine polypeptide sequence, or (b) expressing a polynucleotide sequence encoding the subunit of the HIV-1 nanoparticle vaccine in a cell line expression system that produces shorter Man3-5GlcNAc2 glycans and/or lacks N-acetylglucosaminyltransferase I. In some embodiments, the entire length of the N-linked glycan chain on the HIV-1 vaccine polypeptide is trimmed. In some other embodiments, the length of the N-linked glycan chain is trimmed by about 50%, about 60%, about 70%, about 80%, or about 90%.
In some methods of the invention, the enzyme used for trimming the glycan chain is an endoglycosidase (Endo) or a peptide/N-glycosidase (PNGase). In some preferred embodiments, the employed enzyme is endoglycosidase H, F1, F2, or F3 (Endo-H, F1, F2, or F3). In some of these embodiments, the HIV-1 nanoparticle vaccine is contacted with the enzyme at room temperature, using an expressed and purified HIV-1 SApNP vaccine. In these methods, the employed HIV-1 vaccine material (protein) is preferably not denatured. In these embodiments, the enzymatic digestion can last for 1 hr, 2 hrs, 3 hrs, 4 hrs, 5 hrs, 6 hrs, or even longer. In some of these embodiments, the employed endo-H vs SApNP ratio is 12,500 units vs. 100 g to ensure complete trimming of N-linked glycans on the surface. In some methods of the invention, the enzyme trimmed HIV-1 SApNP vaccine is further subject to protein purification.
In some embodiments, the HIV-1 vaccine for glycan trimming contains a polypeptide sequence having from the N-terminus to the C-terminus (1) the subunit sequence of an HIV-1 Env-derived trimer, (2) the subunit sequence of a self-assembling nanoparticle, and (3) a locking domain subunit sequence. In some of these methods, the employed locking domain subunit sequence is fused to C-terminus of the nanoparticle subunit sequence via a linker sequence. In some embodiments, the linker sequence between the locking domain and the nanoparticle subunit contains GGGGS (SEQ ID NO:3). In some embodiments, the polypeptide sequence of the HIV-1 vaccine additionally contains a pan-reactive T-cell epitope that is fused to the C-terminus of the locking domain subunit sequence. In some of these embodiments, the employed T-cell epitope has the sequence AKFVAAWTLKAAA (SEQ ID NO:7). In some embodiments, the HIV-1 trimer subunit sequence is fused to the nanoparticle subunit sequence via a linker sequence. In some of these embodiments, the linker between the HIV-1 trimmer sequence and the nanoparticle sequence contains the sequence (GaSb)n, wherein a is an integer of 1 to 5, b is an integer of 1 to 2, and n is an integer of 1 to 5.
In various embodiments, the displaying nanoparticle scaffold of the HIV-1 vaccine contains a trimeric sequence. In some of these embodiments, the subunit sequence of the self-assembling nanoparticle contains SEQ ID NO:1 (E2p) or SEQ ID NO:2 (13-01 variant), a conservatively modified variant or a substantially identical sequence thereof. In some embodiments, the employed HIV-1 nanoparticle vaccine displays an uncleaved prefusion-optimized (UFO) HIV-1 gp140 trimer. In some of these embodiments, the UFO gp140 trimer is a chimeric trimer containing a modified gp41ECTO domain from HIV-1 strain BG505. In some of these embodiments, the subunit sequence of the UFO gp140 trimer contains the sequence shown in SEQ ID NO:4, a conservatively modified variant or a substantially identical sequence thereof.
In some embodiments, the polypeptide sequence from which the HIV-1 vaccine is formed contains from the N-terminus to the C-terminus: HIV-1 Env-derived UFO gp140 trimer subunit as shown in SEQ ID NO:4, self-assembling nanoparticle subunit as shown in SEQ ID NO:1 (E2p), the locking domain as shown in SEQ ID NO:5 (LD4), and T-cell epitope AKFVAAWTLKAAA (SEQ ID NO:7). In some of these embodiments, the polypeptide sequence further contains a first linker sequence (GGGGS)2 (SEQ ID NO:8) between the gp140 trimer subunit and the nanoparticle subunit, and/or a second linker sequence GGGGS (SEQ ID NO:3) between the nanoparticle subunit and the locking domain. In some other embodiments, the polypeptide sequence from which the HIV-1 vaccine is formed contains from the N-terminus to the C-terminus: HIV-1 Env-derived UFO gp140 trimer as shown in SEQ ID NO:4, self-assembling nanoparticle subunit as shown in SEQ ID NO:2 (13-01 variant), the locking domain as shown in SEQ ID NO:6 (LD7), and T-cell epitope AKFVAAWTLKAAA (SEQ ID NO:7). In some of these embodiments, the polypeptide sequence further contains a first linker sequence (GGGGS)2 (SEQ ID NO:8) between the gp140 trimer subunit and the nanoparticle subunit, and/or a second linker sequence GGGGS (SEQ ID NO:3) between the nanoparticle subunit and the locking domain.
In some methods of the invention, glycan trimming is achieved by the expressing the HIV-1 vaccine construct in Sf9 insect cell or HEK293F GnTI-cells.
In a related aspect, the invention provides HIV-1 Env trimer nanoparticle vaccines that are produced by a process containing the steps of: (1) expressing a polynucleotide encoding subunit of the HIV-1 nanoparticle composition to generate a self-assembling nanoparticle (SApNP) vaccine, and (2) trimming N-glycosylation chain on the expressed HIV-1 SApNP vaccine with an enzyme. In some embodiments, the enzyme employed for trimming the glycan chain is endoglycosidase H, F1, F2, or F3 (Endo-H, F1, F2, or F3). In some of these embodiments, the process further contains the step of purification of the expressed nanoparticle vaccine prior to the glycan trimming. In some related embodiments, the invention provides pharmaceutical compositions that contain a glycan-trimmed HIV-1 Env trimer nanoparticle vaccine described herein, and a pharmaceutically acceptable carrier. In a related aspect, the invention provides methods for treating or preventing HIV-1 infection in a subject. The methods entail administering to a human subject in need of treatment the pharmaceutical composition of the invention.
A further understanding of the nature and advantages of the present invention may be realized by reference to the remaining portions of the specification and claims.
A main bottleneck of HIV-1 vaccine development is the low immunogenicity of the vaccines in eliciting neutralizing antibody response in vivo. In a 2015 study, the BG505 SOSIP trimer was tested thoroughly in wildtype mice with different adjuvants, immunization routes, and slow-release devices (e.g., osmotic pumps), but failed to induce any detectable tier-2 neutralizing antibody response (Hu et al., J Virol 2015, 89: 10383-10398). In rabbits, both SOSIP and NFL trimers induced tier-2 neutralizing antibody responses that mainly target the glycan holes on the Env. In non-human primates (NHPs), these stable trimers only induced sporadic tier-2 neutralizing antibody responses. It was previously demonstrated that trimer-presenting SApNPs can induce a potent tier-2 neutralizing antibody response in wildtype mice and rabbits (He et al., Sci Adv 2018, 4: aau6769). However, despite the advancements attributed to rational trimer design and nanoparticle display, tier-2 neutralizing antibody responses are only sporadic, with most animals showing negligible or no neutralizing antibody response.
HIV-1 Env is heavily glycosylated, with ˜30 glycans per protomer and ˜90 glycans per trimer, which contribute to ˜50% of the mass and form a dense glycan shield on the surface. Broadly neutralizing antibodies (bNAbs) isolated from elite patients can be categorized based on their epitopes, including the trimeric V2 apex, V3 stem, CD4-binding site (CD4bs), gp120-gp41 interface, and the membrane-proximal external region (MPER). The V2 apex- and V3 stem-directed antibodies constitute a large portion of serum response in the cohort analysis of HIV-1 patients who have developed bNAbs. Notably, a hallmark of the V2 apex- and V3 stem-directed bNAbs is that they must interact with N-linked glycans at specific positions within or around the epitope. For example, the V2-directed bNAbs, such as PG9, PG16, and PGT145, require a Man8-9GlcNac2 glycan structure at N160 for neutralization and may involve the hybrid-type glycans at N173 and N156. The V3 stem-directed bNAbs, such as PGT121, PGT124, PGT128, and PGT135, require a Man8-9GlycNac2 glycan structure at N332 for neutralization and may involve glycans at N295, N301, and other sites. Due to the involvement of multiple glycans, the V3 stem epitope is also called a glycan supersite. Therefore, altering or trimming glycans is generally thought to impair Env binding to glycan-reactive bNAbs, as demonstrated for the PG9 and PG16 antibodies (Doores et al., J. Virol. 84:10510-21, 2010). There are reports that glycan trimming improved immunogenicity of the soluble influenza hemagglutinin trimers. See, e.g., de Vries et al., J. Virol. 86:16735-44, 2012; and Wang et al., Proc. Natl. Acad. Sci. USA 106:18137-42, 2009. However, there has been no actual evidence or subsequent reports that gly can trimming would indeed improve activities of NP-displayed influenza vaccines, let alone HIV-1 NP vaccines. Instead, because N-linked glycans have been considered in the art an integral part of Env epitope structure (See, e.g., Crispin et al., Annu. Rev. Biophys, 2018), N-linked glycans have been exploited as an important target in HIV-1 vaccine design. See, e.g., Doores, FEBS J, 282: 467:9-91, 2015; and Wagh et al., Curr. Opin. HIV AIDS, 15:267-74, 2020. Consistently, one strategy that is gaining popularity in HIV-1 vaccine design is to increase Env glycan occupancy to mimic native viral spike. See, e.g., Derking et al, Cell Rep, 35:108933, 2021.
The present invention is predicated in part on the studies undertaken by the inventors to increase the frequency of vaccine-responders (FVR) after vaccination (e.g., from ˜10% to ˜50% or greater), which would allow the generation of more effective HIV-1 vaccines. The inventors explored various approaches and surprisingly discovered that, contrary to what the consensus view in HIV-1 vaccine field would strongly suggest, a simple “glycan-trimming” step during nanoparticle-based vaccine production process can dramatically increase the FVR of UFO trimer-presenting SApNPs, rendering them highly immunogenic. It was unexpectedly observed that glycan trimming by enzymatic treatment exhibited no adverse effect on the biochemical, biophysical, and antigenic properties of UFO trimer-presenting SApNPs. As detailed herein, HIV-1 UFO trimer-presenting SApNPs can be processed enzymatically to trim N-linked glycans on the Env trimers to expose the most conserved CD4 binding site (CD4bs) and other protein epitopes. Specifically, it was observed by the inventors that glycan trimming is independent of the nanoparticle platforms and Env backbones, as exemplified with HIV-1 BG505 UFO trimer presented on an E2p (SEQ ID NO:1) and an 13-01 variant (SEQ ID NO:2) nanoparticle scaffolds. The glycan trimming significantly increased the vaccine immunogenicity and induced potent neutralizing antibody responses. Importantly, it was observed that nearly identical in vitro outcomes were obtained with two UFO trimer vaccines based on different nanoparticle scaffolds, as evidenced by results from SEC, SDS-PAGE, ns-EM, and BLI. In mouse immunization, potent neutralizing antibody response was observed for both nanoparticle scaffolds after glycan trimming, and the frequency of vaccine responders (FVR) appeared to be notably increased for the 13-01 scaffold (SEQ ID NO:2). While only BG505 UFO trimer-presenting nanoparticle vaccines were exemplified in the studies, this glycan trimming approach could be equally effective for SApNP vaccines derived from non-BG505 Env backbones as Endo-H has been widely used to trim Env glycans for crystallization.
The glycan-trimmed HIV-1 UFO trimer-presenting SApNPs of the invention can be used as prime and/or boost immunogens in preventive HIV-1 vaccines to enhance immunogenicity and increase the frequency of vaccine responders. Glycan trimming by Endo-H can be easily included as an additional step in the down-stream process and expected to deliver materials with high purity, high structural homogeneity, consistent glycan profiles, and improved antigenicity, thus enabling large-scale industrial production in a GMP facility.
Unless otherwise specified herein, compositions and methods related to the glycan trimmed HIV-1 vaccines of the invention can all be generated or performed in accordance with the procedures exemplified herein or routinely practiced methods well known in the art. See, e.g., Methods in Enzymology, Volume 289: Solid-Phase Peptide Synthesis, J. N. Abelson, M. I. Simon, G. B. Fields (Editors), Academic Press; 1st edition (1997) (ISBN-13: 978-0121821906); U.S. Pat. Nos. 4,965,343, and 5,849,954; Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press, N.Y., (3rd ed., 2000); Brent et al., Current Protocols in Molecular Biology, John Wiley & Sons, Inc. (ringbou ed., 2003); Davis et al., Basic Methods in Molecular Biology, Elsevier Science Publishing, Inc., New York, USA (1986); or Methods in Enzymology: Guide to Molecular Cloning Techniques Vol. 152, S. L. Berger and A. R. Kimmerl Eds., Academic Press Inc., San Diego, USA (1987); Current Protocols in Protein Science (CPPS) (John E. Coligan, et. al., ed., John Wiley and Sons, Inc.), Current Protocols in Cell Biology (CPCB) (Juan S. Bonifacino et. al. ed., John Wiley and Sons, Inc.), and Culture of Animal Cells: A Manual of Basic Technique by R. Ian Freshney, Publisher: Wiley-Liss; 5th edition (2005), Animal Cell Culture Methods (Methods in Cell Biology, Vol. 57, Jennie P. Mather and David Barnes editors, Academic Press, 1st edition, 1998). The following sections provide additional guidance for practicing the compositions and methods of the present invention.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by those of ordinary skill in the art to which this invention pertains. The following references provide one of skill with a general definition of many of the terms used in this invention: Academic Press Dictionary of Science and Technology, Morris (Ed.), Academic Press (1st ed., 1992); Oxford Dictionary of Biochemistry and Molecular Biology, Smith et al. (Eds.), Oxford University Press (revised ed., 2000); Encyclopaedic Dictionary of Chemistry, Kumar (Ed.), Anmol Publications Pvt. Ltd. (2002); Dictionary of Microbiology and Molecular Biology, Singleton et al. (Eds.), John Wiley & Sons (3rd ed., 2002); Dictionary of Chemistry, Hunt (Ed.), Routledge (1st ed., 1999); Dictionary of Pharmaceutical Medicine, Nahler (Ed.), Springer-Verlag Telos (1994); Dictionary of Organic Chemistry, Kumar and Anandand (Eds.), Anmol Publications Pvt. Ltd. (2002); and A Dictionary of Biology (Oxford Paperback Reference), Martin and Hine (Eds.), Oxford University Press (4th ed., 2000). Further clarifications of some of these terms as they apply specifically to this invention are provided herein.
As used herein, the singular forms “a,” “an,” and “the,” refer to both the singular as well as plural, unless the context clearly indicates otherwise. For example, “an Env-derived trimer” can refer to both single or plural Env-derived trimer molecules, and can be considered equivalent to the phrase “at least one Env-derived trimer.”
As used herein, the terms “antigen” or “immunogen” are used interchangeably to refer to a substance, typically a protein, which is capable of inducing an immune response in a subject. The term also refers to proteins that are immunologically active in the sense that once administered to a subject (either directly or by administering to the subject a nucleotide sequence or vector that encodes the protein) is able to evoke an immune response of the humoral and/or cellular type directed against that protein. Unless otherwise noted, the term “vaccine immunogen” is used interchangeably with “protein antigen” or “immunogen polypeptide”.
The term “conservatively modified variant” applies to both amino acid and nucleic acid sequences. With respect to particular nucleic acid sequences, conservatively modified variants refers to those nucleic acids which encode identical or essentially identical amino acid sequences, or where the nucleic acid does not encode an amino acid sequence, to essentially identical sequences. Because of the degeneracy of the genetic code, a large number of functionally identical nucleic acids encode any given protein. For polypeptide sequences, “conservatively modified variants” refer to a variant which has conservative amino acid substitutions, amino acid residues replaced with other amino acid residue having a side chain with a similar charge. Families of amino acid residues having side chains with similar charges have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine).
Epitope refers to an antigenic determinant. These are particular chemical groups or peptide sequences on a molecule that are antigenic, such that they elicit a specific immune response, for example, an epitope is the region of an antigen to which B and/or T cells respond. Epitopes can be formed both from contiguous amino acids or noncontiguous amino acids juxtaposed by tertiary folding of a protein.
Effective amount of a vaccine or other agent that is sufficient to generate a desired response, such as reduce or eliminate a sign or symptom of a condition or disease, such as AIDS. For instance, this can be the amount necessary to inhibit viral replication or to measurably alter outward symptoms of the viral infection, such as increase of T cell counts in the case of an HIV-1 infection. In general, this amount will be sufficient to measurably inhibit virus (for example, HIV) replication or infectivity. When administered to a subject, a dosage will generally be used that will achieve target tissue concentrations (for example, in lymphocytes) that has been shown to achieve in vitro inhibition of viral replication. In some embodiments, an “effective amount” is one that treats (including prophylaxis) one or more symptoms and/or underlying causes of any of a disorder or disease, for example to treat HIV-1 infection. In some embodiments, an effective amount is a therapeutically effective amount. In some embodiments, an effective amount is an amount that prevents one or more signs or symptoms of a particular disease or condition from developing, such as one or more signs or symptoms associated with AIDS.
As used herein, a fusion protein is a recombinant protein containing amino acid sequence from at least two unrelated proteins that have been joined together, via a peptide bond, to make a single protein. The unrelated amino acid sequences can be joined directly to each other or they can be joined using a linker sequence. As used herein, proteins are unrelated, if their amino acid sequences are not normally found joined together via a peptide bond in their natural environment(s) (e.g., inside a cell). For example, the amino acid sequences of bacterial enzymes such as B. stearothermophilus dihydrolipoyl acyltransferase (E2p) and the amino acid sequences of HIV-1 gp120 or gp41 glycoproteins are not normally found joined together via a peptide bond.
A heptad repeat (HR) refers to a structural motif that consists of a repeating pattern of seven amino acids: a b c d e f g H P H C P C. where H represents hydrophobic residues, C represents, typically, charged residues, and P represents polar (and, therefore, hydrophilic) residues.
HIV-1 envelope protein (Env) is initially synthesized as a longer precursor protein of 845-870 amino acids in size, designated gp160. gp160 forms a homotrimer and undergoes glycosylation within the Golgi apparatus. In vivo, gp160 glycoprotein is endo-proteolytically processed to the mature envelope glycoproteins gp120 and gp41, which are noncovalently associated with each other in a complex on the surface of the virus. The gp120 surface protein contains the high affinity binding site for human CD4, the primary receptor for HIV, as well as domains that interact with fusion coreceptors, such as the chemokine receptors CCR5 and CXCR4. The gp41 protein spans the viral membrane and contains at its amino-terminus a sequence of amino acids important for the fusion of viral and cellular membranes. The native, fusion-competent form of the HIV-1 envelope glycoprotein complex is a trimeric structure composed of three gp120 and three gp41 subunits. The receptor-binding (CD4 and co-receptor) sites are located in the gp120 moieties, whereas the fusion peptides are located in the gp41 components. Exemplary sequence of wildtype gp160 polypeptides are shown in GenBank, e.g., under accession numbers AAB05604 and AAD12142.
gp140 refers to an oligomeric form of HIV envelope protein, which contains all of gp120 and the entire gp41 ectodomain. As used herein, an HIV-1 gp140 trimer immunogen typically contains a gp140 domain and a modified or redesigned ectodomain of gp140 (gp41ECTO).
gp120 is an envelope protein of the Human Immunodeficiency Virus (HIV). gp120 contains most of the external, surface-exposed, domains of the HIV envelope glycoprotein complex, and it is gp120 which binds both to cellular CD4 receptors and to cellular chemokine receptors (such as CCR5). The mature gp120 wildtype polypeptides have about 500 amino acids in the primary sequence. Gp120 is heavily N-glycosylated giving rise to an apparent molecular weight of 120 kD. The polypeptide is comprised of five conserved regions (C1-05) and five regions of high variability (V1-V5). In its tertiary structure, the gp120 glycoprotein is comprised of three major structural domains (the outer domain, the inner domain, and the bridging sheet) plus the variable loops. See, e.g., Wyatt et al., Nature 393, 705-711, 1998; and Kwong et al., Nature 393, 649-59, 1998. The inner domain is believed to interact with the gp41 envelope glycoprotein, while the outer domain is exposed on the assembled envelope glycoprotein trimer.
Variable region 1 and Variable Region 2 (VT/V2 domain) of gp120 are comprised of about 50-90 residues which contain two of the most variable portions of HIV-1 (the V1 loop and the V2 loop), and one in ten residues of the V1/V2 domain are N-glycosylated.
gp41 is a proteolytic product of the precursor HIV envelope protein. It contains an N-terminal fusion peptide (FP), a transmembrane domain, as well as an ectodomain that links the fusion peptide and a transmembrane domain. gp41 remains in a trimeric configuration and interacts with gp120 in a non-covalent manner. The amino acid sequence of an exemplary gp41 is set forth in GenBank, under Accession No. CAD20975.
BG505 SOSIP.664 gp140 is an HIV-1 Env immunogen developed with the gp140 trimer from clade-A strain BG505. It contains a covalent linkage between the cleaved gp120 and gp41ECTO with an engineered disulfide bond (termed SOS). In addition, it has an I559P mutation (termed IP) to destabilize the gp41 post-fusion conformation and also a truncation of the membrane-proximal external region (MPER) at residue 664 to improve solubility. This HIV-1 immunogen has an outstanding antigenic profile and excellent structural mimicry of the native spike. Using the SOSIP trimer as a sorting probe, new bNAbs have been identified and characterized. The SOSIP design has also been extended to other HIV-1 strains and permitted the incorporation of additional stabilizing mutations. Recently, immunogenicity of SOSIP trimers in rabbits and nonhuman primates was reported, paving the way for human vaccine trials.
Immunogen is a protein or a portion thereof that is capable of inducing an immune response in a mammal, such as a mammal infected or at risk of infection with a pathogen. Administration of an immunogen can lead to protective immunity and/or proactive immunity against a pathogen of interest.
Immune response refers to a response of a cell of the immune system, such as a B cell, T cell, or monocyte, to a stimulus. In some embodiment, the response is specific for a particular antigen (an “antigen-specific response”). In some embodiments, an immune response is a T cell response, such as a CD4+ response or a CD8+ response. In some other embodiments, the response is a B cell response, and results in the production of specific antibodies.
Immunogenic composition refers to a composition comprising an immunogenic polypeptide that induces a measurable CTL response against virus expressing the immunogenic polypeptide, or induces a measurable B cell response (such as production of antibodies) against the immunogenic polypeptide.
Sequence identity or similarity between two or more nucleic acid sequences, or two or more amino acid sequences, is expressed in terms of the identity or similarity between the sequences. Sequence identity can be measured in terms of percentage identity; the higher the percentage, the more identical the sequences are. Two sequences are “substantially identical” if two sequences have a specified percentage of amino acid residues or nucleotides that are the same (i.e., 60% identity, optionally 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 99% identity over a specified region, or, when not specified, over the entire sequence), when compared and aligned for maximum correspondence over a comparison window, or designated region as measured using one of the following sequence comparison algorithms or by manual alignment and visual inspection. Optionally, the identity exists over a region that is at least about 50 nucleotides (or 10 amino acids) in length, or more preferably over a region that is 100 to 500 or 1000 or more nucleotides (or 20, 50, 200 or more amino acids) in length.
Homologs or orthologs of nucleic acid or amino acid sequences possess a relatively high degree of sequence identity/similarity when aligned using standard methods. Methods of alignment of sequences for comparison are well known in the art. Various programs and alignment algorithms are described in: Smith & Waterman, Adv. Appl. Math. 2:482, 1981; Needleman & Wunsch, J. Mol. Biol. 48:443, 1970; Pearson & Lipman, Proc. Natl. Acad. Sci. USA 85:2444, 1988; Higgins & Sharp, Gene, 73:237-44, 1988; Higgins & Sharp, CABIOS 5:151-3, 1989; Corpet et al., Nuc. Acids Res. 16:10881-90, 1988; Huang et al. Computer Appls. in the Biosciences 8, 155-65, 1992; and Pearson et al., Meth. Mol. Bio. 24:307-31, 1994. Altschul et al., J. Mol. Biol. 215:403-10, 1990, presents a detailed consideration of sequence alignment methods and homology calculations.
N-linked glycosylation is the attachment of an oligosaccharide, a carbohydrate consisting of several sugar molecules, sometimes also referred to as glycan, to a nitrogen atom (the amide nitrogen) of an asparagine (Asn) residue of a protein. This type of linkage is important for both the structure and function of many eukaryotic proteins. The N-linked glycosylation process occurs in eukaryotes and widely in archaea, but very rarely in bacteria. The nature of N-linked glycans attached to a glycoprotein is determined by the protein and the cell in which it is expressed. It also varies across species. Different species synthesize different types of N-linked glycan.
The term “subject” refers to any animal classified as a mammal, e.g., human and non-human mammals. Examples of non-human animals include dogs, cats, cattle, horses, sheep, pigs, goats, rabbits, and etc. Unless otherwise noted, the terms “patient” or “subject” are used herein interchangeably. Preferably, the subject is human.
The term “treating” or “alleviating” includes the administration of compounds or agents to a subject to prevent or delay the onset of the symptoms, complications, or biochemical indicia of a disease (e.g., an HIV infection), alleviating the symptoms or arresting or inhibiting further development of the disease, condition, or disorder. Subjects in need of treatment include those already suffering from the disease or disorder as well as those being at risk of developing the disorder. Treatment may be prophylactic (to prevent or delay the onset of the disease, or to prevent the manifestation of clinical or subclinical symptoms thereof) or therapeutic suppression or alleviation of symptoms after the manifestation of the disease.
As used herein, uncleaved pre-fusion-optimized (UFO) trimers refer to HIV-1 gp140 trimeric proteins that are formed with gp120 protein and a redesigned gp41ECTO domain, which results in more stabilized HIV-1 gp140 trimers (
Vaccine refers to a pharmaceutical composition that elicits a prophylactic or therapeutic immune response in a subject. In some cases, the immune response is a protective immune response. Typically, a vaccine elicits an antigen-specific immune response to an antigen of a pathogen, for example a viral pathogen, or to a cellular constituent correlated with a pathological condition. A vaccine may include a polynucleotide (such as a nucleic acid encoding a disclosed antigen), a peptide or polypeptide (such as a disclosed antigen), a virus, a cell or one or more cellular constituents. In some embodiments of the invention, vaccines or vaccine immunogens or vaccine compositions are expressed from fusion constructs and self-assemble into nanoparticles displaying an immunogen polypeptide or protein on the surface.
Virus-like particle (VLP) refers to a non-replicating, viral shell, derived from any of several viruses. VLPs are generally composed of one or more viral proteins, such as, but not limited to, those proteins referred to as capsid, coat, shell, surface and/or envelope proteins, or particle-forming polypeptides derived from these proteins. VLPs can form spontaneously upon recombinant expression of the protein in an appropriate expression system. Methods for producing particular VLPs are known in the art. The presence of VLPs following recombinant expression of viral proteins can be detected using conventional techniques known in the art, such as by electron microscopy, biophysical characterization, and the like. See, for example, Baker et al. (1991) Biophys. J. 60:1445-1456; and Hagensee et al. (1994) J. Virol. 68:4503-4505. For example, VLPs can be isolated by density gradient centrifugation and/or identified by characteristic density banding. Alternatively, cryoelectron microscopy can be performed on vitrified aqueous samples of the VLP preparation in question, and images recorded under appropriate exposure conditions.
A self-assembling nanoparticle refers to a ball-shape protein shell with a diameter of tens of nanometers and well-defined surface geometry that is formed by identical copies of a non-viral protein capable of automatically assembling into a nanoparticle with a similar appearance to VLPs. Known examples include ferritin (FR), which is conserved across species and forms a 24-mer, as well as B. stearothermophilus dihydrolipoyl acyltransferase (E2p), Aquifex aeolicus lumazine synthase (LS), and Thermotoga maritima encapsulin, which all form 60-mers. Self-assembling nanoparticles can form spontaneously upon recombinant expression of the protein in an appropriate expression system. Methods for nanoparticle production, detection, and characterization can be conducted using the same techniques developed for VLPs.
The invention relates to methods for producing HIV-1 nanoparticle vaccines with trimmed or shortened N-linked glycan chains, and vaccine compositions thus produced. As demonstrated herein, the HIV-1 vaccines with trimmed or shortened glycan chains have enhanced immunogenicity and neutralizing antibody inducing activities. In various embodiments, HIV-1 nanoparticle vaccines with trimmed or shortened glycan chains can be produced by either post-expression enzymatic treatment of vaccine proteins or expression of the vaccine constructs in an expression system that lacks normal glycosylation function for human proteins. Typically, the HIV-1 vaccines for glycan trimming or shortening in the practice of the present invention contain an HIV-1 Env derived trimer protein that is displayed on a self-assembling nanoparticle scaffold.
Any Env-derived HIV-1 trimer proteins can be used in the starting HIV-1 nanoparticle vaccines for glycan trimming or shortening. The Env-derived trimer protein can be obtained from various HIV-1 strains. In some embodiments, the nanoparticles present a native trimeric form of HIV-1 Env based glycoproteins or domains, e.g., gp140, gp120 or V1V2 domains. In some embodiments, the employed HIV-1 Env-derived trimer protein is an uncleaved prefusion-optimized (UFO) gp140 trimer. In some embodiments, the Env-derived trimer is from HIV-1 strain BG505, e.g., the BG505. SOSIP.664 gp140 trimer. In some preferred embodiments, the starting nanoparticles present a modified gp140 trimer immunogen, e.g., a HR1-modified gp140 trimer (“UFO trimer”) described in Kong et al., Nat. Comm. 7, 12040, 2016. The amino acid sequence of subunit of this HR1-modified gp140 trimer protein is shown in SEQ ID NO:4. In some embodiments, the HIV-1 trimeric immunogen displayed in the starting nanoparticle vaccine in the invention can be a UFO2-BG trimer. UFO2-BG trimers are chimeric gp140 trimers containing (1) the BG505 gp41 domain with a redesigned HR1 N-terminal bend and a cleavage-site linker (as described in Kong et al., Nat. Comm. 7, 12040, 2016) and (2) the gp120 protein from one of other diverse HIV-1 strains or subtypes. In addition to the redesigned gp41ECTO domain from the BG505 strain, the gp41 domain in the chimeric gp140 trimers suitable for the invention can also be a consensus gp41ECTO domain derived from the HIV-1 sequence database. Many other HIV-1 Env derived trimer sequences known in the art can also be used in the starting nanoparticle vaccines of the invention. See, e.g., WO2017/192434, WO2019/089817, and WO2019/241483. Also can be used in constructing the starting HIV-1 nanoparticle vaccines in the practice of the invention are conservatively modified variants of the various HIV-1 trimer proteins described herein, or variants with substantially identical sequences thereof.
The displaying scaffold used in the starting HIV-1 vaccines for practicing the methods of the invention can be any self-assembling nanoparticle sequence. In general, the nanoparticles employed in the invention need to be formed by multiple copies of a single subunit. In some preferred embodiments, the employed self-assembling nanoparticles are derived from ferritin (FR), E2p and I3-01 as exemplified herein. Examples of these scaffold sequences are shown in SEQ ID NOs:1 and 2. Other suitable scaffold sequences are also known in the art. See, e.g., WO2017/192434, WO2019/089817, and WO2019/241483. Two starting HIV-1 nanoparticle vaccines, which respectively utilize an E2p derived scaffold sequence (SEQ ID NO:1) and an I3-01 variant scaffold sequence (SEQ ID NO:2), are exemplified herein. In various embodiments, the starting HIV-1 nanoparticle vaccines for practicing methods of the invention can employ any of these known nanoparticle scaffolds, as well as their conservatively modified variants or variants with substantially identical (e.g., at least 90%, 95% or 99% identical) sequences.
In addition to the HIV-1 Env trimer and the displaying scaffold, the starting nanoparticle vaccines can also contain other structural components. In some embodiments, a locking domain is fused at the C-terminus to the nanoparticle sequence. The locking domain functions to stabilize the nanoparticles from the inside in displaying the immunogen protein or polypeptide (e.g., Env-derived HIV-1 trimer protein). In general, the locking domain can be any protein capable of forming a dimer. Typically, the locking domain is covalently fused to the nanoparticle subunit to which the immunogen polypeptide (e.g., subunit of an HIV-1 Env derived trimer protein) is linked. Many proteins known in the art can be employed as the locking domain in the practice of the invention. See, e.g., WO2019/241483. Two specific locking domain sequences (SEQ ID NO:5 and SEQ ID NO:6) are present in the starting HIV-1 SApNP vaccines exemplified herein.
In some embodiments, the starting HIV-1 SApNP vaccines for glycan trimming or shortening can additionally contain a T-cell epitope to promote robust T-cell responses and to steer B cell development towards bNAbs. The T-cell epitope can be located at any position in relation to the other structural components so long as it does not impact presentation of the immunogen polypeptides on the nanoparticle surface. In some preferred embodiments, the T-cell epitope is located at the C-terminus of the nanoparticle subunit, e.g., by fusing the N-terminus of the T-cell epitope to the C-terminus of the locking domain subunit sequence, as exemplified in the nanoparticle vaccines described in the Examples herein. Any T helper epitope known in the art can be used in constructing the starting vaccine compositions in the practice of the invention. See, e.g., Alexander et al., Immunity 1, 751-761, 1994; Ahlers et al., J. Clin. Invest. 108:1677-1685, 2001; Fraser et al., Vaccine 32, 2896-2903, 2014; De Groot et al., Immunol. Cell Biol. 8:255-269, 2002; and Smahel et al., Gene Ther. 21: 225-232, 2014. In some preferred embodiments, the employed T-helper epitope is the universal pan-reactive T-cell epitope peptide, AKFVAAWTLKAAA (SEQ ID NO:7).
In various embodiments, nanparticles displaying any of the immunogen polypeptides or proteins described herein (e.g., HIV-1 Env-derived trimer immunogens) can be constructed by fusing the immunogen polypeptide or subunit of multimeric immunogen protein (e.g., a trimer immunogen) to the subunit of the nanoparticle (e.g., E2p or I3-01 subunit) and the locking domain, as well as the other optional or alternative components as needed or helpful (e.g., linker moieties or foldon). To construct the nanoparticle displayed fusion vaccine immunogens of the invention, one or more linker motifs or moieties may be employed to facilitate connection and maintain structural integrity of the different components. Thus, in some embodiments, a linker motif can be employed to connect the C-terminus of the immunogen polypeptide (e.g., HIV-1 trimer protein subunit) to the N-terminus of the nanoparticle subunit. Additionally or alternatively, a second linker motif can be used to link the C-terminus of the nanoparticle subunit (or the C-terminus of the immunogen polypeptide) to the N-terminus of the locking domain. In some other embodiments, a third linker motif may be employed to connect the T-cell epitope, e.g., linking the C-terminus of the locking domain to the N-terminus of the T-cell epitope, or linking the C-terminus of the T-cell epitope to the N-terminus of the locking domain. In some embodiments, linkers can also be used to insert a neck domain or a foldon domain into the nanoparticle vaccine constructs. Typically, the linker motifs contain short peptide sequences. In various embodiments, the linkers or linker motifs can be any flexible peptides that connect two protein domains without interfering with their functions. For example, any of these linkers used in the constructs can be GC-rich peptides with a sequence of (GaSb)n, wherein a is an integer of about 1-5, b is an integer of about 0-2, and n is an integer of about 1-5. In some other embodiments, a T-cell epitope can be used as a linker or part of a linker between the C-terminus of the immunogen polypeptide and the N-terminus of the nanoparticle subunit.
The starting HIV-1 vaccine compositions in the practice of the invention can be constructed recombinantly in accordance with methods that have been described in the art, e.g., WO2019/089817; WO2019/241483; He et al., Nat. Comm. 7, 12041, 2016; Kong et al., Nat. Comm. 7, 12040, 2016; and He et al., Sci Adv. 4(11): eaau6769, 2018. As exemplification, two specific HIV-1 nanoparticle vaccine constructs are described herein. The first construct expresses a fusion polypeptide that contains from the N-terminus to the C-terminus: HIV-1 UFO BG505.SOSIP.664 gp140 subunit sequence, E2p nanoparticle subunit sequence (e.g., SEQ ID NO:1), a linker motif (GaSb)n noted above (e.g., (GGGGS)2 (SEQ ID NO: 8)), a locking domain as shown in SEQ ID NO:5 (LD4), and a T-cell epitope (e.g., the PADRE epitope shown in SEQ ID NO:7). Optionally, the immunogen polypeptide (e.g., gp140 subunit for HIV-1 vaccine) can be connected to the nanoparticle subunit (e.g., E2p) via a linker sequence, e.g., GGGGS (SEQ ID NO:3) or (GGGGS)2 (e.g., SEQ ID NO:8). The second construct expresses a fusion polypeptide that contains from the N-terminus to the C-terminus: HIV-1 UFO BG505.SOSIP.664 gp140, a linker sequence (GGGGS)2 (SEQ ID NO:8), 13-01 nanoparticle subunit sequence (SEQ ID NO:2), a second linker (GaSb)n noted above (e.g., GGGGS (SEQ ID NO:3)), a locking domain as shown in SEQ ID NO:6 (LD7), and a T-cell epitope (e.g., the epitope as shown in SEQ ID NO:7). Optionally, a dipeptide linker, GS, can be inserted between the locking domain and the T-cell epitope in any of these vaccine constructs. The antigeniciy and structural integrity of the vaccine immunogens (e.g., HIV-1 nanoparticle immunogens) can be readily analyzed via standard assays, e.g., antibody binding assays and negative-stain electron microscopy (EM). As exemplified herein, the fusion molecules can all self-assemble into nanoparticles that display immunogenic epitopes of the Env-derived trimer (e.g., gp140).
The invention provides methods for generating HIV-1 nanoparticle vaccines with trimmed or shortened N-linked glycan chains on the surface of the displayed HIV-1 trimer protein, as well as related HIV-1 vaccine compositions thus produced. In some embodiments, the methods involve post-expression trimming of the glycan chains on the vaccine proteins. As demonstrated herein, the glycan trimming step can significantly increase the vaccine immunogenicity and induce potent neutralizing antibody responses in more subjects during vaccination. In some embodiments, glycan trimming of the HIV-1 nanoparticle vaccines is achieved via enzymatic digestion. In these embodiments, the expressed and optionally purified vaccines are subject to in vitro glycan-trimming with an enzyme. Any enzyme that is capable of digesting the N-linked glycan chain on the HIV-1 trimer proteins can be employed in the practice of the invention. In general, glycan chains can be trimmed with glycosidases which catalyze the hydrolysis of glycosidic bonds to remove sugars from proteins. These enzymes are critical for glycan processing in the ER and Golgi, and each enzyme shows specificity for removing a particular sugar (e.g., mannosidase).
In some preferred embodiments, the enzyme to be used is endoglycosidase H (Endo-H), which cleaves within the chitobiose core of high mannose and some hybrid oligosaccharides from N-linked glycoproteins. Endo-H is a 29 kD protein isolated from Streptomyces plicatus or Streptomyces griseus. Structure and activities of this enzyme are well known in the art. See, e.g., Robbins et al., J. Biol. Chem. 259: 7577-83, 1984; and Trimble et al., Analy. Chem. 141: 515-22, 1984. It cleaves the bond in the diacetylchitobiose core of the oligosaccharide between two N-acetylglucosamine (GlcNAc) subunits directly proximal to the asparagine residue, generating a truncated sugar molecule with one N-acetylglucosamine residue remaining on the asparagine. It deglycosylates mannose glycoproteins, but the extent and rate of the deglycosylation depends to a high degree on the nature of the glycoproteins. The deglycosylation rate can be increased by denaturation of the glycoproteins (e.g., by carboxymethylation, sulfitolysis or by heating in the presence of sodium dodecyl sulfate). The addition of 2-mercaptoethanol can significantly increase the enzyme's activity against glycoproteins containing inter- or intra-molecular disulfide bridges, unlike detergents like Triton X-100, n-Octylglucoside, or zwitterionic detergents. In the practice of the invention, the Endo-H enzyme can be readily obtained from commercial vendors, e.g., New England BioLabs. Glycan trimming of the HIV-1 vaccine proteins with the enzyme can be performed according to the instructions of the enzyme manufacturer (e.g., New England BioLabs). Optionally, some minor modifications of the standard protocols can be implemented to ensure desired digestion of the N-linked glycan chain on the HIV-1 trimer immunogen polypeptides displayed on the nanoparticle scaffolds.
In various embodiments, the N-linked glycan chains on the displayed HIV-1 trimer protein are trimmed or shortened to different degrees. In some embodiments, the entire glycan chains are trimmed. In some of these embodiments, the Endo-H treatment can be conducted at room temperature (e.g., at 25° C.) using purified SApNP vaccine material without denaturing. In some of these embodiments, the maximum enzyme/vaccine protein ratio suggested by the enzyme manufacturer is used to ensure the most complete enzymatic digestion of N-linked glycans on the immunogen protein surface. For example, as exemplified herein with the Ep2 or I3-01 displayed HIV-1 BG505 UFO trimer nanoparticle vaccines, 12,500 units or 25 μl of the enzyme (New England BioLabs) can be used to treat 100 μg of the purified vaccine proteins. In some embodiments, a less than complete trimming of the glycan chain is desired. For example, the trimming can entail shortening of the glycan chain by about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% of its length. In some of these embodiments, a lesser enzyme/protein ratio may be used to achieve a desired degree of glycan trimming. For example, for 100 μg of the HIV-1 SApNP material (e.g., the exemplified Ep2 or 13-01 displayed HIV-1 BG505 UFO trimer SApNP vaccines), 10,000 units (20 μl), 7,500 units (15 μl), 5,000 units (10 μl), 2,500 units (5 μl), 1,250 units (2.5 μl) or even less of the exemplified Endo-H enzyme may be used. In still some other embodiments, a desired degree of glycan trimming can be achieved by adjusting the length of period for the enzymatic action. For example, to ensure proper and/or complete enzymatic processing, the reaction can last for at least 0.5 hr, 1 hr, 2 hrs, 3 hrs, 4 hrs, 5 hrs, 6, hrs, 7 hrs, 8 hrs, 9 hrs, 10 hrs, 15 hrs, 20 hrs or longer. In various embodiments, the enzymatic digestion can last from about 1 hr to about 8 hrs, from about 2 hrs to about 6 hrs, or from 3 hrs to about 4 hrs. In some embodiments, the amount of the enzyme used and the treatment time should enable a substantial reduction of the length of the glycan chains on the nanoparticle displayed HIV-1 trimer protein. In various embodiments, the enzymatic treatment should lead to a shortening of the glycan chains by at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% of their length. In these embodiments, substantially all glycan chains (e.g., at least 75%, at least 85%, at least 95% or all) present on the surface of the displayed HIV-1 trimer protein are shortened by the noted extent.
In addition to varying the condition of the enzymatic digestion (e.g., length of reaction time, amount of enzyme used and etc.), extent of glycan trimming can also be controlled by the use of different enzymes. Several classes of enzymes can be used alone, in combination, or in a particular sequential order to achieve different levels of glycan trimming by cleaving off residues from the tip of a glycan chain towards the Asp residue to which an N-linked glycan chain is attached. For example, Peptide/N-glycosidase F (PNGase F) cleaves between the innermost GlcNAc and Asparagine residues of high mannose, hybrid, and complex oligosaccharides, resulting in complete deglycosylation of an N-linked glycoproteins (100% trimming). PNGase F is sensitive to protein structure and may not cleave some or all of glycans unless the glycoprotein is fully denatured. Endoglycosidases (Endo) cleave between the N-acetylglucosamine residues within the glycan core and leave one N-acetylglucosamine residue on the Asparagine (approximately 70-90% trimming). These include, e.g., Endo-H noted above, as well as Endo-F1, F2 and F3. Endo-F1 and Endo-H cleave oligomannose and hybrid glycans, while Endo-F2 and Endo-F3 prefer to cleave complex glycans. Other enzymes, such as neuraminidase, β-galactosidase, N-acetylglucosaminidase, and fucosidases, can be used sequentially to trim a complex oligosaccharide to Man3GlcNAc2 (approximately 50-70% trimming). Therefore, glycan trimming to desirable levels can be achieved by using these enzymes in their functional conditions to cleave off residual groups from N-linked glycans. The ranges of optimal temperature, pH, and digestion time are well-documented for these enzymes.
Following glycan trimming, the processed vaccine material can be further subject to purification. Any standard or well-known protein purification methods may be employed in the practice of the invention. In some embodiments, the glycan trimmed vaccines can be purified via size-exclusion chromatography (SEC). For example, as exemplified herein, the Endo-H treated vaccines can be purified on a Superose 6 column. Additional routinely practiced protein purification techniques or other polishing steps can also be used in the purification of the glycan-trimmed HIV-1 nanoparticle vaccine compositions described herein. These include, e.g., centrifugation, separation based on charge or hydrophobicity, affinity chromatography, and immunoaffinity chromatography.
Other than enzymatic trimming of post-expression vaccine protein materials, HIV-1 nanoparticle vaccine compositions with trimmed or shortened glycan chains can also be obtained by expressing the vaccine constructs in cell lines or expressing systems without normal post-translational N-glycosylation function. For example, most prokaryotic expression systems such as E. coli cannot carry out post-translational modifications. Non-human mammalian expression systems such as CHO or NS0 cells have the machinery required to add complex, human-type glycans. However, glycans produced in these systems can differ from glycans produced in humans, as they can be capped with both N-glycolylneuraminic acid (Neu5Gc) and N-acetylneuraminic acid (Neu5Ac), whereas human cells only produce glycoproteins containing N-acetylneuraminic acid.
In some embodiments, the HIV-1 nanoparticle vaccines without normal glycan chains can be produced by the expressing the vaccine constructs in Sf9 insect cells. Proteins produced from these insect cells contain shorter Man3GlcNAc2 glycans. In some other embodiments, the HIV-1 vaccines nanoparticle vaccines without normal glycan chains can be produced by the expressing the vaccine constructs in HEK293F GnTI-cells. These cells do not have N-acetylglucosaminyltransferase I (GnTI) activity, lack complex N-glycans, and produce Man5-9GlcNAc2 glycans.
The glycan trimmed HIV-1 nanoparticle vaccines described herein and related pharmaceutical compositions can be used in prophylactic and therapeutic applications for treating or preventing HIV-1 infections. In the practice of the therapeutic methods of the invention, the subjects in need of prevention or treatment of HIV-1 infection is administered with an effective amount of the glycan trimmed vaccine or pharmaceutical composition. The administered pharmaceutical composition can be either a therapeutic formulation or a prophylactic formulation. Typically, the composition additionally includes one or more pharmaceutically acceptable vehicles and, optionally, other therapeutic ingredients (for example, antibiotics or antiviral drugs). Various pharmaceutically acceptable additives can also be used in the compositions.
For therapeutic applications, appropriate adjuvants can be additionally included in the glycan trimmed HIV-1 vaccine compositions of the invention. Examples of suitable adjuvants include, e.g., aluminum hydroxide, lecithin, Freund's adjuvant, MPL™ and IL-12. In some embodiments, the vaccine compositions can be formulated as a controlled-release or time-release formulation. This can be achieved in a composition that contains a slow release polymer or via a microencapsulated delivery system or bioadhesive gel. The various pharmaceutical compositions can be prepared in accordance with standard procedures well known in the art. See, e.g., Remington's Pharmaceutical Sciences, 19th Ed., Mack Publishing Company, Easton, Pa., 1995; Sustained and Controlled Release Drug Delivery Systems, J. R. Robinson, ed., Marcel Dekker, Inc., New York, 1978); U.S. Pat. Nos. 4,652,441 and 4,917,893; 4,677,191 and 4,728,721; and 4,675,189.
In some therapeutic applications of the invention, a glycan trimmed HIV-1 nanoparticle vaccine composition can be administered to a subject to induce an immune response to HIV-1, e.g., to induce production of broadly neutralizing antibodies to HIV-1. For subjects at risk of developing an HIV infection, a vaccine composition of the invention can be administered to provide prophylactic protection against viral infection. Depending on the specific subject and conditions, pharmaceutical compositions of the invention can be administered to subjects by a variety of administration modes known to the person of ordinary skill in the art, for example, intramuscular, subcutaneous, intravenous, intra-arterial, intra-articular, intraperitoneal, or parenteral routes. In general, the pharmaceutical composition is administered to a subject in need of such treatment for a time and under conditions sufficient to prevent, inhibit, and/or ameliorate an HIV-1 infection. The immunogenic composition is administered in an amount sufficient to induce an immune response against HIV-1. For therapeutic applications, the compositions should contain a therapeutically effective amount of the glycan trimmed HIV-1 nanoparticle immunogen described herein. For prophylactic applications, the compositions should contain a prophylactically effective amount of the glycan trimmed HIV-1 nanoparticle immunogen described herein. The appropriate amount of the immunogen can be determined based on the specific disease or condition to be treated or prevented, severity, age of the subject, and other personal attributes of the specific subject (e.g., the general state of the subject's health and the robustness of the subject's immune system). Determination of effective dosages is additionally guided with animal model studies followed up by human clinical trials and is guided by administration protocols that significantly reduce the occurrence or severity of targeted disease symptoms or conditions in the subject.
For prophylactic applications, the immunogenic composition is provided in advance of any symptom, for example in advance of infection. The prophylactic administration of the immunogenic compositions serves to prevent or ameliorate any subsequent infection. Thus, in some embodiments, a subject to be treated is one who has, or is at risk for developing, an HIV-1 infection, for example because of exposure or the possibility of exposure to the HV-1 virus. Following administration of a therapeutically effective amount of the disclosed therapeutic compositions, the subject can be monitored for an infection, symptoms associated with an HIV-1 infection, or both.
For therapeutic applications, the immunogenic composition is provided at or after the onset of a symptom of disease or infection, for example after development of a symptom of infection, or after diagnosis of the infection. The immunogenic composition can thus be provided prior to the anticipated exposure to HIV virus so as to attenuate the anticipated severity, duration or extent of an infection and/or associated disease symptoms, after exposure or suspected exposure to the virus, or after the actual initiation of an infection.
The pharmaceutical composition of the invention can be combined with other agents known in the art for treating or preventing HIV-1 infections. For example, these known agents include, e.g., antibodies or other antiviral agents such as nucleoside reverse transcriptase inhibitors, such as abacavir, AZT, didanosine, emtricitabine, lamivudine, stavudine, tenofovir, zalcitabine, zidovudine, and the like, non-nucleoside reverse transcriptase inhibitors, such as delavirdine, efavirenz, nevirapine, protease inhibitors such as amprenavir, atazanavir, indinavir, lopinavir, nelfinavir, osamprenavir, ritonavir, saquinavir, tipranavir, and the like, and fusion protein inhibitors such as enfuvirtide and the like. Administration of the pharmaceutical composition and the known anti-HIV agents can be either concurrently or sequentially.
The glycan-trimmed HIV-1 nanoparticle vaccine compositions of the invention or pharmaceutical compositions of the invention can be provided as components of a kit. Optionally, such a kit includes additional components including packaging, instructions and various other reagents, such as buffers, substrates, antibodies or ligands, such as control antibodies or ligands, and detection reagents. An optional instruction sheet can be additionally provided in the kits.
The following examples are offered to illustrate, but not to limit the present invention.
Two HIV-1 BG505 UFO trimer-presenting nanoparticle vaccine constructs were expressed and purified for glycan trimming studies. One of the SApNPs is formed of a polypeptide chain sequence containing from the N-terminus to the C-terminus: BG505 UFO trimer (SEQ ID NO:4), E2p nanoparticle subunit sequence (SEQ ID NO:1), a locking domain subunit sequence (SEQ ID NO:5), and a T-cell epitope (SEQ ID NO:7). The second SApNP is formed of a polypeptide chain sequence containing from the N-terminus to the C-terminus: BG505 UFO trimer (SEQ ID NO:4), a GS rich linker sequence (SEQ ID NO:8), 13-01 variant nanoparticle subunit sequence (SEQ ID NO:2), a locking domain subunit sequence (SEQ ID NO:6), and a T-cell epitope (SEQ ID NO:7). More detailed information about the structure, construction and activities of these HIV-1 UFO-trimer nanoparticle vaccine constructs are described in the art, e.g., WO2019/241483.
The BG505 UFO trimer-presenting SApNPs can be produced in various CHO cells. In laboratory-scale production, they can be transiently expressed in ExpiCHO cells (Thermo Fisher). In large-scale production, they can be either transiently expressed in CHO-S cells or stably expressed in CHO-K1 cells. Immunoaffinity chromatography (IAC) columns based on human antibodies PGT145 and 2G12 was used to purify SApNPs from the CHO cell supernatant, followed by size-exclusion chromatography (SEC) on a Superose 6 column with other polishing steps.
The purified SApNP material is subjected to glycan-trimming by Endo-H, which is followed by SEC purification on a Superose 6 column with other polishing steps. The Endo-H treatment is performed according to the manufacturer's instructions (New England BioLabs) with minor changes. Specifically, the treatment is conducted at room temperature (25° C.) using purified SApNP material without denaturing for 4 hr. The maximum SApNP vs. endo-H ratio (100 g vs. 12,500 units or 25 μl) in the manual is used to ensure the most complete enzymatic digestion of N-linked glycans on the surface.
Following Endo-H treatment, glycan-trimmed SApNPs can be purified from the SApNP/Endo-H/glycan mix by SEC on a Superose 6 column. In a recent study, we processed the CHO-K1-produced SApNPs with Endo-H and purified the glycan-trimmed SApNPs using a Superose 6 column (
Although a lower band was observed for the Endo-H-treated SApNPs in SDS-PAGE, a higher-precision analysis is needed to confirm the trimming effect for all the N-linked glycosylation sites in the BG505 Env sequence. To this end, we determined the site-specific glycosylation and occupancy profiles for both E2p and I3-01v9-based SApNPs, with and without Endo-H treatment (
Because the particulate structure of SApNP vaccines is the key to their superior immune response, whether Endo-H treatment has any adverse effect on the structural stability of SApNP must be investigated. To this end, we performed negative-stain electron microscopy (ns-EM) analysis on two SApNP vaccines following Endo-H treatment and SEC purification in several repeated experiments (
Following structural characterization by ns-EM, we assessed the antigenicity of glycan-trimmed SApNPs by bio-layer interferometry (BLI) on an Octet RED96 instrument using representative human neutralizing antibodies (
We performed a mouse study to determine the immunogenicity of glycan-trimmed BG505 UFO trimer-presenting SApNPs. Briefly, 4 groups of BALB/c mice, 8 mice per group, were immunized with E2p and I3-01v9-based SApNPs with 3-week intervals. Two prime-boost regimens were tested. In regimen #1 (homologous), mice received 4 doses of glycan-trimmed SApNP, whereas in regimen #2 (heterologous), mice were primed with 2 doses of glycan-trimmed SApNP and then boosted with 2 doses of wildtype SApNP. In this study, the E2p-based SApNP is formulated with AddaVax, an oil-in-water type of adjuvant, whereas the I3-01v9-based SApNP is mixed with aluminum phosphate. Serum samples before immunization and 2 weeks after each dose were collected for antigen binding assays based on enzyme-linked immunoassay (ELISA) and for neutralization assays after IgG purification.
After sample collection, purified mouse IgG were tested in TZM-bl pseudovirus neutralization assays against tier-2 BG505.T332N, other tier-2 isolates in the global virus panel, and selected tier-1 isolates. Specifically, mouse IgGs from the last time point (week 11) were tested against BG505.T332N, with a 300 g/ml starting concentration followed by a series of 3-fold dilutions (
The invention thus has been disclosed broadly and illustrated in reference to representative embodiments described above. It is understood that various modifications can be made to the present invention without departing from the spirit and scope thereof.
It is further noted that all publications, sequence accession numbers, patents and patent applications cited herein are hereby expressly incorporated by reference in their entirety and for all purposes as if each is individually so denoted. Definitions that are contained in text incorporated by reference are excluded to the extent that they contradict definitions in this disclosure.
This invention was made with government support under Contract Number AI129698 awarded by the National Institutes of Health. The government has certain rights in the invention.
