Patent Application
20190135876
The present application is being filed along with a Sequence Listing in electronic format. The Sequence Listing is provided as a file entitled 388512013700SeqList, which was created Oct. 12, 2018 and is 17,500 bytes in size. The information in the electronic format of the Sequence Listing is incorporated by reference in its entirety.
In general, the field of the invention is the treatment of infectious disease. More specifically, the field is prophylaxis and treatment of respiratory syncytial virus (RSV) infection. Epitopes of broadly neutralizing monoclonal antibodies defined by high resolution structural analysis enable design of optimized immunogens and screening tools for discovery of treatments. Further, the field includes treatment of defective host immune function by mimicry of respiratory syncytial virus.
RSV is a negative-strand RNA virus with 10 genes encoding 11 proteins, which has resisted effective management for over 60 years in part because infection does not provide robust immunity {Broadbent, L. et al. Influenza Other Respir Viruses (2015) 9:169-78}. To date, no vaccine has been approved despite several substantial attempts {Jorquera, P. A. and Tripp, R. A. Expert Rev Respir Med (2017) 11(8):609-615}. Over 50% of infants in the US are infected during their first year, with nearly 5% requiring hospitalization {American Academy of Pediatrics Committee on Infectious Diseases, American Academy of Pediatrics Bronchiolitis Guidelines. Pediatrics (2014) 134:e620-38}. Severe RSV disease in infancy is an established risk factor for childhood asthma-like symptoms {Gelfand, E. W. Curr Opin Immunol (2012) 24(6):713-9}. The only care available for RSV infection is supportive. Preterm infants (<29 weeks gestational age) have been the focus for prophylaxis with a humanized mouse mAb (palivizumab, marketed by MedImmune as Synagis®), an expensive treatment which reduces morbidity but not mortality {Meissner, H. C. and Kimberlin, D. W. Pediatrics (2013) 132:915-8}. Palivizumab has not been shown to be safe and effective for post-infection treatment {Malley, R. et al. J Infect Dis (1998) 178:1555-61}. Global incidence of RSV infection in young children is less well documented than in the US but is believed to be more than double that of US, with higher mortality rates {Nair H., et al. Lancet (2010) 375(9725):1545-1555}. In addition, up to 12% of medically attended acute respiratory illness in older adults is attributed to RSV infection with 6-8% of these cases being lethal. Hospitalizations last 3 to 6 days, with a substantial fraction admitted to the intensive care unit {Colosia, A. D., et al. PLoS ONE. (2017) 12(8):e0182321}. RSV infections are also common in immunocompromised patients with mortality of over 25% {Shah, D. P., et al. Blood (2014) 123(21):3263-3268}.
RSV has two major surface glycoproteins, F and G. The sole marketed mAb against RSV (Synagis®, described above) is only approved for prophylactic use in premature infants, and is directed against the F protein. This mAb is broadly useful due to conservation of the F protein sequence among strains. By contrast, the G protein overall is quite variable, although a region in the middle of the sequence is highly conserved. Two subtypes of RSV, A and B, circulate alternately at ˜1-2-year intervals, with comparable incidence worldwide.
Initial attempts at prophylaxis for RSV by vaccination with formalin-inactivated RSV proved counterproductive, leading to enhanced disease and pulmonary eosinophilia {Kim, H. W., et al. Am J Epidemiol (1969) 89:422-434}. U.S. Pat. No. 8,173,131 discloses compositions that include the CX3C chemokine motif in the RSV G protein for prevention and treatment of RSV infection, both as interfering agents for modulating RSV infection by tying up the relevant receptor or for inducing immunity. This motif is required for successful infection by RSV {Jeong, K. I., et al. PLoS One (2015) 10(6):e0130517}. U.S. Pat. No. 8,846,056 discloses immunogenic peptides from RSV G protein as vaccine components, specifically including residues 164-176 or 155-206. U.S. Pat. No. 9,321,830 discloses mAbs useful in treating RSV infections that bind to conserved linear sequences of the G protein of RSV in the region including residues 167-176; as these antibodies were derived from the natural human immune repertoire, they are expected to be minimally immunogenic when administered to a human subject. About 15% of the RSV G protein is secreted due to use of an alternative translation start site at codon 48 that eliminates the cytoplasmic domain and a portion of the transmembrane domain region {Hendricks, D. A., et al. J Virol (1988) 62:2228-33}. Deletion of this start site considerably reduces virulence {Stobart, C. C., et al. Nat Commun (2016) 7:13916}, {Arnold, R., et al Virology (2004) 330:384-397}. This is significant since high affinity for antigen is needed for neutralizing soluble factors {Tabrizi, M., et al. AAPS J (2010) 12:33-43}, and therefore mAbs with low pM affinity such as those disclosed in U.S. Pat. No. 9,321,830 are advantageous.
Collarini, E. J., et al. J Immunol (2009) 183:6338-45 describes high affinity, broadly neutralizing mAbs that bind to the RSV G protein central conserved region (CCR) as well as antibodies with varying affinities including 3D3 (1.1 pM), 2B11 (10 pM), 3G12 (580 pM), 5D8 (4.4 nM). The epitopes defined by these mAbs are of particular interest since human antibodies are particularly favorable from both an efficacy perspective (having been cloned from healthy donors) and a safety perspective (reduced chance of off-target reactivity that would create toxicity). The mAb 3D3 has shown broad neutralizing activity both in vitro and in rodent models; the epitope for 3D3 defined at the level of short linear peptides is highly conserved across nearly all circulating strains. An additional mAb, 2D10, is of interest since no linear peptide epitope could be defined for it although it is active in viral neutralization assays in vitro, albeit with lower potency than 3D3 {U.S. Pat. No. 8,273,354}. These antibodies as well as 3G12 are employed in determining the utility described above.
The contents of these documents and all documents cited herein are incorporated herein by reference.
A recombinant fusion protein comprising the central region (residues 131-230) of the G proteins of both RSV A and B subtypes was shown to be an effective immunogen in mice {Lee, J. Y. and Chang, J. PLoS One (2017) 12:e0175384}. A G protein peptide, residues 148-198 emulsified in DMSO and PBS, has also been tested in mice as an immunogen and found to be effective at inducing antibodies that both neutralize infection and block G protein binding to CX3CR1 {Choi, Y., et al. Viral Immunol (2012) 25(3):193-203}. Similarly, vaccination with nanoparticles that incorporate the G protein residues 169-198 induced protection in mice challenged with RSV {Jorquera, P. A., et al. PLoS One (2013) 8:e74905}. Fine scale optimization of peptides from this region has also been attempted, with insertion of one extra residue into the G protein at residues 182-186 greatly reducing the deleterious effects of G protein on the host immune response {Boyoglu-Barnum, S., et al. J Virol (2017) 91(10) pii: e02059-16}.
Although these results are encouraging, no RSV G protein vaccine has been approved. Repeated infection is common for this virus, unlike many others. The immunosuppressive properties of the G protein may be responsible for this effect. Criteria defining quality of an immunogen, for which further improvements are useful, include: uniformity of response (titer and affinity) across a diverse human population; stability (particularly important for use in countries lacking an effective refrigerated supply chain); specificity (active against all circulating strains), and safety (in particular, lack of deleterious pharmacological activity on the CX3C chemokine receptor); and duration of response. Design of improved vaccine components is one of the aspects of the present invention, based ultimately on interaction of conformational epitopes of the G protein with antibodies of known affinity.
Despite the important role of the RSV G protein in RSV infection and disease, almost no structural information has been described for this protein. Only the NMR solution structure of the 16 amino acid RSV G cysteine noose has been determined {Sugawara, M., et al. J Pept Res (2002) 60:271-282}.
The structures of peptides from the CCR of the G protein complexed with mAbs 3D3, 2D10 and 3G12 have now been determined at high resolution by x-ray crystallography and establish that amino acids 161-197, (SEQ ID NO:1) that includes the key functional region of RSV G, is located at the apex of the G glycoprotein, rendering it accessible to antibody binding.
The present invention relates to compositions related to epitopes on the G protein from respiratory syncytial virus (RSV) revealed by crystallographic studies of high affinity, broadly neutralizing monoclonal antibodies (mAbs) bound to peptides derived from the conserved central region (CCR) of the G protein that is known to interact with host cell factors. These compositions include peptides and other binding moieties that mimic specifically portions of the central conserved region (CCR) of the G protein that also includes a region that is known to interact with host cell factors, including the CX3C receptor (CX3CR1). More specifically, RSV G protein is organized as an N-terminal cytosolic region, a transmembrane region, and a variable ectodomain consisting of two mucin-like domains separated by a non-glycosylated central conserved region (CCR). The CCR contains four cysteine residues that form a cysteine noose, formed by disulfide bonds between a.a. 173-186 that further comprises a cystine loop at a.a. 176-182 and a CX3C chemokine motif (a.a. 182-186). Specific peptides or peptidomimetics derived from the epitopes in this region may be used as immunogens or as tools for discovery of binding agents capable of neutralizing RSV. The invention also comprises epitope mimics that accentuate immunogenicity while minimizing pharmacological activity or vice versa.
A deleterious pharmacological activity of a G protein vaccine is interaction with CX3CR1, which leads to undesirable side effects such as inflammation. Peptide-based vaccines that include a functional CX3CR1 binding site may thus stimulate this undesirable result. As shown below, the three dimensional structure of the interaction of G protein with high affinity antibodies permits the identification of conserved residues of the CCR that can be modified to inactivate the CX3CR1 binding site and decrease or obliterate this effect without compromising the immunogenicity of the vaccine. As used herein, “modified peptide” and “mutant” are used interchangeably.
Thus, in one aspect, the invention is directed to mutants of the G protein or of peptides comprising all or a portion of the CCR thereof that are immunogenic but lack the ability to activate CX3CR1. These mutants can be designed by identifying amino acids that are contained within the CCR of the G protein and which do not participate in the binding of high affinity antibodies and substituting for them amino acids with side chains of different shape or size or charge, thus inhibiting the binding of the RSV G mutant to the receptor without interfering with the immunogenicity of the peptide or protein. In particular, the invention is directed to a peptide (including full length RSV G protein) that contains at least one amino acid substitution at position 162, 164, 166, 177, 187, and/or 193 of the RSV G protein and that shows reduced chemotactic activity as compared to wild type RSV G protein.
In another aspect, the invention relates to a peptide having the amino acid sequence of residues 161-197 of respiratory syncytial virus (RSV) G protein (SEQ ID NO:1) or the amino acid sequence of positions 162-172 (SEQ ID NO:2) or of positions 169-198 (SEQ ID NO:3) or of positions 157-197 (SEQ ID NO:4) or of positions 148-197 (SEQ ID NO:5) or of positions 161-195 (SEQ ID NO:6), each chemically stabilized to retain the conformation exhibited upon binding to antibody.
An alternative immunogen is a molecule that comprises at least two covalently linked components, wherein said components are peptides of the amino acid sequence SEQ ID NO:2 and/or the amino acid sequence of SEQ ID NO:3 or wherein each of said components is the corresponding mutant or peptidomimetic of SEQ ID NO:2 and/or SEQ ID NO:3.
Peptide embodiments of the invention such as those that mimic soluble RSV G antigens or peptides that are binding moieties can be prepared recombinantly. Peptides that mimic antigens may thus be generated easily to facilitate comprehensive mutational analysis to identify variants within the CCR that can reduce or enhance immunogenicity or provide activation or inhibition of the CX3CR1 receptor.
In another aspect, the invention provides a mutant or peptidomimetic of the peptide of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6 that has enhanced immunogenicity as compared to the respective peptide of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6, including embodiments wherein the conformation of said mutant is chemically stabilized.
In some applications, reduced immunogenicity is advantageous, thus the invention also includes mutant or peptidomimetic of the peptides of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6 that has reduced immunogenicity as compared to the respective peptide of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6 including embodiments wherein the conformation of said mutant is chemically stabilized.
Agents that either inhibit or activate the C3XCR1 receptor, but have low immunogenicity can enhance or suppress immune responses generally (including those unrelated to RSV infection). Thus in another aspect the invention is directed to a mutant or peptidomimetic of peptides of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6 that stimulates or inhibits the chemokine receptor CX3CR1 responsive to fractalkine, especially, wherein this mutant or peptidomimetic has reduced immunogenicity as compared to the respective peptide of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6. A suitable in vitro functional analysis interaction of a candidate moiety of the host chemokine receptor CX3CR1 is also disclosed.
Also disclosed is a method for assessing fidelity of test compounds such as peptidomimetics and mutant peptide variants to the disclosed conformational epitope. The method includes measuring the relative binding strength of the peptidomimetics or mutants to mAbs that vary in affinity for the native protein. Agents that bind preferentially to mAbs with high affinity for the native protein are more likely to induce such antibodies than agents that preferentially bind to mAbs with weaker affinity or that have weak affinity for the optimal mAb.
Thus another aspect of the invention is a method to identify immunogens useful in vaccines which method comprises contacting a candidate molecule with mAb 3D3, mAb 2D10 or mAb 3G12 or an antigen-binding fragment thereof and with at least one binding moiety that binds with low affinity to the RSV G protein, whereby a candidate molecule that preferentially binds to 3D3, mAb 2D10 or mAb 3G12 is identified as having said desirable properties as an immunogen. The invention also includes molecules thus identified which may be aptamers or members of a combinatorial library of small molecules or of peptides.
In yet another aspect, the conformational epitope mimics, whether recombinant peptides or peptidomimetics, provide useful tools for discovery of homogeneous compositions of non-immunoglobulin binding moieties with activity similar to the known broadly neutralizing mAbs. Thus the invention includes a method to identify a binding moiety that has the characteristics of strain independence, high affinity for the conserved region of the RSV G protein and neutralizing activity which method comprises contacting a candidate binding moiety with a conformationally restrained form of a peptide having the amino acid sequence of any one of SEQ ID NOs:1-6 as shown in
The invention further includes methods to provide prophylactic or therapeutic treatment with respect to RSV infection in a subject which method comprises administering to a subject in need of such treatment pharmaceutical or veterinary composition including the immunogens or binding moieties of the invention. The invention also includes methods to treat immune mediated inflammatory diseases, chronic pain and peripheral neuropathy which method comprises administering to a subject in need of such treatment compounds of the invention that interact with the C3XC receptor. These, too, may be included in pharmaceutical or veterinary compositions.
For the first time, high resolution structural data have been obtained for the interaction of high affinity, broadly neutralizing monoclonal antibodies (mAbs) and peptides derived from the conserved central region (CCR) of RSV G protein. These results provide a foundation for rational engineering of an immunogen as has been shown for other viruses {Sharon, J., et al. Immunology (2014) 142(1):1-23}. The novel structures define two neighboring conformational epitopes on RSV G CCR, that include helices, disulfide bonds, and polar and hydrophobic interactions between discontinuous amino acids. These results illuminate why linear RSV G epitope peptides and misfolded RSV G are not likely to be fully effective as antigens; for example, an early attempt to target the CCR of the G protein with a recombinant protein vaccine (BBG2Na) showed only a moderate ability to induce neutralizing antibodies in healthy, young adults and a more recent effort also using recombinant G protein failed to establish efficacy in elderly adults {Rezaee, F., et al. Curr Opin Virol (2017) 24:70-78}. Mapping of sequence conservation onto the RSV G structure defines a large three-dimensional region on the RSV surface that is highly conserved.
These conformational features of the disclosed peptides or mutants can be stabilized by use of chemical crosslinkers or non-natural amino acids {Robinson, J. A. J Pept Sci (2013) 19(3):127-40}.
As shown in Example 5 the Fab of 3D3 complexed to RSV G[162-172] (SEQ ID NO:2) was determined to 2.40 Å-resolution. The RSV G[162-172] peptide contains a short helix and projects several hydrophobic residues, including Phe163, Phe165, Phe168, Phe170 and Pro172, into a ˜700 Å2 groove formed by heavy-chain complementarity-determining regions (CDRs) 1, 2, and 3 and light-chain CDRs 1 and 3. Surprisingly, the distal six amino acids of the extended heavy-chain CDR3 formed no molecular contacts with the linear epitope peptide. A larger fragment of RSV G (RSV G[161-197]) (SEQ ID NO:1) was produced in E. coli and the structure of that complex determined to 2.40 Å-resolution. Additional interactions with 3D3 included heavy-chain CDR3 contacts with the RSV G cysteine noose (residues 173-186) as well as additional interactions between heavy-chain CDRs 1 and 2 and RSV G residues 189-190. Altogether, 3D3 binds to RSV G at a discontinuous, conformational epitope comprising ˜1,060 Å2, designated as antigenic site γ1.
The mAb 2D10 also binds RSV G but its epitope could not be characterized by linear epitope mapping. A recombinant single-chain variable fragment (scFv) of 2D10 forms stable complexes with a synthetic RSV G peptide (RSV G[169-198] SEQ ID NO:3), and as also shown in Example 5 the crystal structure of the complex was determined to 1.56 Å-resolution. The mAb 2D10 uses a twisted heavy-chain CDR3, heavy-chain CDR2, and light-chain CDR3 to bind to a ˜550 Å2 epitope on the RSV G cysteine noose. The CX3C chemokine motif, which forms a short helix in the cysteine noose, is buried by 2D10 binding. Although the 2D10 epitope is comprised mainly of residues 177-188, and is thus technically continuous, the cysteine noose comprises two nested disulfide bonds that induce strong conformational character to this epitope, designated as antigenic site γ2.
The three dimensional conformations of the three peptides used for these studies superimpose nearly identically. A diverse set of RSV G sequences was used to map conservation level onto this consensus RSV G structure. Despite overall high variability of full-length RSV G (53% identity between subtypes RSV A and B), the 37 amino acid fragment RSV G[161-197] contains 24 invariant residues (70% identity between subtypes RSV A and B). Notably, in the CX3C motif only one of the three “X” amino acids, Ile185, is highly conserved, implying that this motif alone does not comprise the CX3CR1-binding site, but the invariant cysteines in the CX3C motif stabilize a three-dimensional surface of highly conserved amino acids that form extensive atomic interactions across the entire region. Many aspects of the invention are derived from these findings.
Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art to which this disclosure belongs.
“Protein”, “peptide” and “polypeptide” are used interchangeably and to refer to chains of naturally occurring amino acids coupled through amide bonds such that they can be synthesized by recombinant methods regardless of the length of the chain. “Peptidomimetics” include unnatural or synthetic amino acids, including D and L isomers and amino acid analogs linked by amide linkages or other bonds, e.g., ester, ether, etc. “Peptidomimetics” also include organic molecules not obviously analogous to peptides, including, for example, aptamers.
As used herein, “binding moiety” includes antibodies and alternative non-immunoglobulin binding moieties as set forth hereinbelow. “Antibodies” include immunoreactive fragments of traditional antibodies and their various fragmented forms that still retain immunospecificity such as Fab, F(abab2, Fv fragments, single-chain antibodies in which the variable regions of heavy and light chain are directly bound without some or all of the constant regions. Also included as “antibodies” are bispecific antibodies which contain a heavy and light chain pair derived from one antibody source and a heavy and light chain pair derived from a different antibody source. Similarly, since light chains are often interchangeable without destroying specificity, antibodies composed of a heavy chain variable region that determines the specificity of the antibody may be combined with a heterologous light chain variable region. Chimeric antibodies with constant and variable regions derived, for example, from different species are also included.
For the variable regions of mAbs, as is well known, the critical amino acid sequences are the CDR sequences arranged on a framework which framework can vary without necessarily affecting specificity or decreasing affinity to an unacceptable level. Definition of these CDR regions is accomplished by art-known methods. Specifically, the most commonly used method for identifying the relevant CDR regions is that of Kabat as disclosed in Wu, T. T., et al., J. Exp. Med. (1970) 132:211-250 and in the book Kabat, E. A., et al. (1983) Sequence of Proteins of Immunological Interest, Bethesda National Institute of Health, 323 pages. Another similar and commonly employed method is that of Chothia, published in Chothia, C., et al., J. Mol. Biol. (1987) 196:901-917 and in Chothia, C., et al., Nature (1989) 342:877-883. An additional modification has been suggested by Abhinandan, K. R., et al., Mol. Immunol. (2008) 45:3832-3839. The mAbs described herein include the CDR regions as defined by any of these systems or other recognized systems known in the art.
The specificities of the binding of mAbs are defined, as noted, by the CDR regions mostly those of the heavy chain, but complemented by those of the light chain as well (the light chains being somewhat interchangeable). Therefore, the mAbs of the invention may contain the three CDR regions of a heavy chain and optionally the three CDR's of a light chain that matches it. Because binding affinity is also determined by the manner in which the CDR's are arranged on a framework, the mAbs may contain complete variable regions of the heavy chain containing the three relevant CDR's as well as, optionally, the complete light chain variable region comprising the three CDR's associated with the light chain complementing the heavy chain in question. This is true with respect to the mAbs that are immunospecific for a single epitope as well as for bispecific antibodies or binding moieties that are able to bind two separate epitopes.
The invention also includes binding moieties that mimic the binding characteristics of mAbs. mAb mimics include aptamers {Yu, Y., et al. Int J Mot Sci (2016) 17(3):358} and protein mimics of antibodies or fragments thereof (alternative scaffolds) such as camelids, anticalins, ankyrin repeat proteins {Azhar A., et al. Int J Blot Macromol (2017) 102:630-641}.
Bispecific binding moieties may be formed by covalently linking two different binding moieties with different specificities. Multiple technologies now exist for making a single antibody-like molecule that incorporates antigen specificity domains from two separate antibodies (bi-specific antibody). Suitable technologies have been described by MacroGenics (Rockville, Md.), Micromet (Bethesda, Md.) and Merrimac (Cambridge, Mass.). (See, e.g., Orcutt, K. D., et al., Protein Eng. Des. Sel. (2010) 23:221-228; Fitzgerald, J., et al., MAbs. (2011) 1:3; Baeuerle, P. A., et al., Cancer Res. (2009) 69:4941-4944). For example, the CDR regions of the heavy and optionally light chain derived from one monospecific mAb may be coupled through any suitable linking means to peptides comprising the CDR regions of the heavy chain sequence and optionally light chain of a second mAb. If the linkage is through an amino acid sequence, the bispecific binding moieties can be produced recombinantly and the nucleic acid encoding the entire bispecific entity expressed recombinantly. As was the case for the binding moieties with a single specificity, the invention also includes the possibility of binding moieties that bind to one or both of the same epitopes as the bispecific antibody or binding entity/binding moiety that actually contains the CDR regions. The invention further includes bispecific constructs which comprise the complete heavy and light chain sequences or the complete heavy chain sequence and at least the CDR's of the light chains or the CDR's of the heavy chains and the complete sequence of the light chains.
In particular, the invention is directed to a mutant or peptidomimetic of a peptide having the amino acid sequence of residues 161-197 of respiratory syncytial virus (RSV) G protein (SEQ ID NO:1) or of positions 169-198 (SEQ ID NO:3), or of positions 157-197 (SEQ ID NO:4), or of positions 148-197 (SEQ ID NO:5), or of positions 161-195 (SEQ ID NO:6) that has diminished activity with respect to activating the chemokine receptor responsive to fractalkine as compared to the respective peptide of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6; that binds mAb 3D3, and/or 2D10 and/or 3G12; and/or wherein said mutant or peptidomimetic elicits antibodies immunoreactive with RSV G protein. In some embodiments the elicited antibodies have sub-nM affinity for an epitope of RSV G protein conserved between A and B strains of the virus.
In some embodiments the peptidomimetic or peptide is chemically stabilized to retain the conformation exhibited upon binding to antibody and/or contains at least one substitution for amino acid 162, 164, 166, 177, 187, 192 and/or of 193 the RSV G protein.
In another embodiment the invention includes a mutant or peptidomimetic of peptide of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6 that stimulates or inhibits the chemokine receptor responsive to fractalkine as compared to the respective peptide of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6. In some embodiments the mutant or peptidomimetic has reduced immunogenicity as compared to the respective peptide of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5 or SEQ ID NO:6.
Any proteins or peptides of the invention may be produced recombinantly using known techniques. The invention also includes nucleic acid molecules comprising nucleotide sequences encoding them, as well as vectors or expression systems that comprise these nucleotide sequences, cells containing expression systems or vectors for expression of these nucleotide sequences and methods to produce the peptides by culturing these cells and recovering the binding moieties produced. Any type of cell typically used in recombinant methods can be employed including prokaryotes, yeast, mammalian cells, insect cells and plant cells. Also included are human cells (e.g., muscle cells or lymphocytes) transformed with one or more recombinant molecules that encode the relevant peptides.
As used herein, “a” or “an” means “at least one” or “one or more.”
Although variable overall, RSV G (298 residues) contains a ˜40 amino acid central conserved region (CCR) that is highly conserved, devoid of glycosylation, and has been shown to play key roles in both virus infection and viral pathogenesis. Specifically, RSV G CCR contains a CX3C chemokine motif that facilitates binding to the human chemokine receptor CX3CR1 to promote RSV infection in human airway epithelial cells as well as modulating signaling that affects trafficking of CX3CR1+ immune cells resulting in airway congestion. For example, treatment with mAbs against the CCD of RSV G protein was associated with a reduction in total lung leukocytes in comparison to isotype control treated mice at day 5 post-inoculation, while treatment with anti-F mAb (Synagis) did not reduce total BAL cells {Caidi, H., et al. Antiviral Research (2018) 154:149-157}.
There are no structural or sequence similarities between RSV G and fractalkine/CX3CL1, the only known ligand for CX3CR1, aside from the presence of a CX3C motif and its two disulfide bonds, as diagrammed in
Alternatively, enhancement of the activity of the CX3CR1 binding motif can be used to create a novel stimulator of this receptor. This is useful for treating diseases such as ulcerative colitis. In mice, CX3CR1 is implicated in preventing the disease-associated translocation of commensal bacteria to mesenteric lymph nodes. CX3CR1-knockout mice and mice deficient in fractalkine both displayed increased translocation of bacteria and markedly increased disease severity in a model of dextran sulfate sodium (DSS)-induced colitis {Medina-Contreras, O., et al. J Clin Invest (2011) 121(12):4787-95}. In addition, CX3CR1 has been shown to be an important regulator of beta-cell function and insulin secretion {Lee, Y. S., et al. Cell (2013) 153(2):413-425}, and the RSV G protein pharmacological motif mimic could thus also be developed as a therapeutic to treat diabetes.
The ability of the stabilized forms of SEQ ID NOs: 1-6 or the mutants or peptidomimetics thereof and their specially constrained forms can be tested for their ability to activate or inhibit the CX3C receptor using, for example, the chemotaxis assay set forth in Example 4 hereinbelow. However, any suitable method for assay could also be used. For use in therapy, it is advantageous for these entities to have relatively low immunogenicity and this too can be tested, for example, using the assays set forth in Example 3, but any suitable test may be used.
Three design goals dominate optimization of a G protein immunogen, each of which is substantially facilitated by the novel structural information.
First, the pharmacological activity of the G protein is deleterious in the context of RSV infection and it is thus preferable to minimize that activity in the immunogen. As noted above, this activity is centered around the C3XC receptor and successful mutants or peptidomimetics can be assessed using the chemotaxis assay, among other assays. The crystallographic studies described in the present invention permit identification of amino acids whose substitution would be useful in diminishing interaction with the C3XC receptor while retaining immunogenic properties which are the second desirable characteristic of a vaccine. Specifically, it has been found that residues 162, 164, 166, 177 and 187 are present in the CCR region of the RSV G protein and/or either a part of or adjacent to the C3XC motif and are not among the residues that specifically bind the high affinity antibodies described herein. Thus, replacing one or more of these residues with an alternative that will either alter the charge or the size and shape of the side chain will interfere with interaction with the C3XC receptor.
Second, high affinity antibodies are needed to neutralize the deleterious soluble G protein produced by virus infected cells, so antibodies generated by the immunogens should have these properties. Affinity can readily be tested using the ELISA assays described in Example 2 or using one of the many alternative methods known in the art. To test for immunogens that will generate antibodies with desirable affinity and neutralization properties, binding to human mAbs that exhibit such desired properties is assessed. As disclosed in Collarini, et al. (supra) mAbs with affinities varying across 3 orders of magnitude, from low pM to low nM: 3D3 (1.1 pM), 2B11 (10 pM), 3G12 (580 pM), 5D8 (4.4 nM) are available for such assays. Candidate immunogens that do not bind well to a high affinity mAb such as 3D3 or 2B11 or that bind better to mAbs with weaker affinity for the natural conformation of the G protein are unlikely to be able to induce production of the desired high affinity mAbs and vice versa.
Third, since RSV is an important pathogen worldwide, including in countries that lack a refrigerated supply chain for delivery of vaccines, stabilization of the immunogen to allow transport and storage at room temperature (or above) is also desirable. Formalin inactivation of live virus, which is effective in other vaccines, is not acceptable for RSV since the first such vaccine caused disease exacerbation upon subsequent natural infection {Kim, H. W., et al. Am J Epidemiol (1969) 89:422-34}.
With respect to this third aspect, conformational stability, as has been shown for the RSV F protein, stabilization of the structure via mutations chosen based on antibody-antigen high resolution structural data results in achieving high titer more uniformly across immunized subjects than for the parental virus {McClellan, J. S., et al. Science (2013) 340(6136): 1113-1117}. Since the G protein CCR can be made either synthetically or recombinantly, methods well known in the art can be used to systematically mutate this peptide. To facilitate evaluation of a large number of such variants, in vitro assays are needed. Suitable assays are known in the art for mAb binding, for evaluation of thermal stability, and for activation of the CX3CR1 receptor.
In addition to the disadvantage of requirement for refrigeration, the use of flexible peptides as immunogens often elicits antibodies that bind weakly (≥micromolar KD) to conformational epitopes in folded proteins. For that reason, conformationally constrained synthetic epitope mimetics are of particular interest in immunogen design, with examples including efforts addressing HIV, hepatitis C, influenza, and others {Robinson, J. A. J Pept Sci (2013) 19(3):127-40}.
Peptides incorporating non-natural motifs are often quite resistant to proteolytic degradation, which is an advantageous feature unrelated to the mimicry itself. A disadvantage of small molecules (“haptens”) is that they are often not immunogenic themselves; however, they can become effective immunogens when presented to the immune system embedded in virus like particles {Buonaguro, L., et al. Exp. Rev. Vaccines (2011) 10: 1569-1583}.
In particular, the F protein of RSV has been subjected to such mimicry. In this instance, two “staples” (crosslinks) were required to create an effective mimic, which displayed nanomolar potency for inhibition of RSV infection in Hep-2 cells in vitro {Gaillard, V., et al. Antimicrob Agents Chemother. (2017) 61(4) pii: e02241-16}.
In addition, constraining the immunogen's three dimensional structure to preserve the high affinity interaction with 3D3 is thus advantageous and a convenient assay is by ELISA binding. Assays for thermal stability known in the literature include observation of increased fluorescence of a dye when bound to hydrophobic sites exposed as the protein unfolds {Biggar, K. K., et al. BioTechniques (2012) 53:231-238} and observation of secondary structure character by circular dichroism {Kelly, S. M. and Price, N.C. Biochim Biophys Acta (1997) 1338(2):161-185}.
As noted above, methods are available in the art to assess candidate mutants and peptidomimetics for appropriate physiological activity, including evaluation of binding activity and neutralization capability employing antibodies of varying affinity. With respect to constructing candidate mutants and peptidomimetics, the detailed structural information provided by the invention enables targeted mutagenesis to identify the key residues needed for immunogenicity (or for pharmacological activity on the host CX3CR1 receptor noted above to design candidate immunogens). Such “molecular dissection” to separate functions is highly advantageous for identifying product candidates. “De-immunization” (reduction in immunogenicity) has been accomplished for the purpose of enabling repeated administration of a foreign protein {Mazor, R., et al. Oncotarget (2016) 7(21):29916-26}. Purely empirical methods, involving mutating each residue in turn and evaluating the result followed by combinations of such mutations, can be augmented by computational analysis to identify the residues most likely to contribute to immunogenicity and replacements that are most likely to reduce immunogenicity {He, L. and Zhu, J. Curr Opin Virol (2015) 11:103-12}. It is already known that insertion of a single additional amino acid within the CX3CR1 motif reduces pharmacological activity {Boyoglu-Barnum, S., et al. J Virol (2017) 91(10) pii: e02059-16}. Further determination of inactivating sites enables reduction in this deleterious activity while retaining immunogenicity leading to viral neutralization.
Although the crystal structures described herein have revealed the surface shape and complementarity of mAb interfaces with the RSV G protein CCR, the energetically important interactions are not directly readable from the structures. In other examples of protein-protein interfaces, certain residues constitute ‘hot-spots’ that make a disproportionately large contribution to binding energy. These privileged sites can be identified by alanine scanning mutagenesis (i.e. creation of variants in which one residue at a time is replaced by alanine) {Robinson, J. A. J Pept Sci (2013) 19(3):127-40}; based on the high resolution structure, certain sites will benefit from substituting a different amino acid rather than alanine.
The mAbs 3D3, 2D10, and 3G12 bind quite differently to the same region, as diagrammed in
An important aspect of the invention is an effective immunogen for inducing mAbs that block the G protein interaction with CX3 CR1, wherein that immunogen itself lacks binding to the receptor. Identifying the residues needed for CX3CR1 binding is accomplished using the same library of variants as for identification of key immunogenic epitopes, but assayed for functionality in a cell based assay for CX3CR1 activation as described in Example 4. Additional variants, such as those that are outside of mAb epitopes but are conserved and predicted to reduce or eliminate CX3CR1 binding, are also useful in this regard. Additional variants, such as insertion of an extra residue in the CX3C motif, may also be candidates.
The conformational epitope mimics, whether recombinant peptides or peptidomimetics, enable efficient discovery of homogeneous compositions of non-immunoglobulin binding moieties with activity similar to the known broadly neutralizing mAbs such as aptamers or alternative scaffolds. Such mimics can provide superior stability, lower cost of manufacture (e.g. by expression in bacterial rather than in mammalian cells), and simpler formulation for inhaled delivery. (The epitope mimics can also be used for identification of additional mAbs.) Homology modeling of the epitope mimics for human RSV can be used to develop analogous epitope mimics for generating mAbs useful in veterinary indications, e.g. to treat bovine RSV infections. Although there is only 30% amino acid identity between the bovine and human RSV G proteins, they share similar features in that the G protein of both viruses has a central conserved cysteine noose region flanked by two more variable domains which are heavily glycosylated {Guzman, E. and Taylor, G. Mol Immunol (2015) 66(1):48-56}.
Libraries of such antibody mimics are evaluated by means of competition assays wherein the mimic is used to compete with mAbs such as 3D3, 2D10 or 3G12 for binding to the RSV G protein itself, or more preferably to an epitope mimic that presents the conformational properties in a stable form. Those candidates that successfully compete with the mAb for the epitope are selected as suitable binding agents. Further optimization can be achieved by rank ordering the candidates with regard to binding to epitope mimics that vary in their fidelity to the optimal conformation. As described above with regard to stabilization of epitope mimics, the fidelity of epitope mimics can be determined by measuring relative affinity for mAbs such as 3D3 or mAbs with lower affinity binding to the same general region of RSV G protein. Binding agents are deemed superior if they show stronger affinity for epitope mimics that in turn display high affinity binding to the known mAbs with broadly neutralizing activity.
The invention is also directed to pharmaceutical and veterinary compositions which comprise as active ingredients the binding moieties, mutants or other peptides or peptidomimetics of the invention. The compositions contain suitable physiologically compatible excipients such as buffers and other simple excipients. The compositions may include additional active ingredients as well, in particular in the case of immunogens immune system stimulants as vaccine adjuvants. The pharmaceutical or veterinary compositions may also contain other formulation excipients, including formulations for intra-nasal or inhaled delivery of mAbs as described in U.S. Pat. No. 9,718,875.
The binding moieties of the invention may also be used in diagnosis.
The immunogens are employed in a method to generate an immune response to RSV, comprising administering formulations containing them to a subject, including a human subject, such as a pregnant woman, an infant, an elderly human, or an immunocompromised subject. The binding moieties of the invention may also be used for therapy or prophylaxis. Infections in other animal species that are related to RSV may also be treated prophylactically or therapeutically by the immunogens or binding moieties of the invention.
Mutants or peptidomimetics that modulate the C3XC receptor are employed in methods to treat other conditions such as rheumatoid arthritis, osteoarthritis, atherosclerosis, diabetes, chronic pain arising from peripheral neuropathy, ulcerative colitis and inflammatory bowel disease.
Recombinant mAbs 3D3 and 2D10 were produced by transient-transfection in CHO cells and purification by immobilized protein A. The CDRs for these mAbs are disclosed in FIG. 5A of U.S. Pat. No. 8,273,354 and single chain Fv sequences are included in those employed in recombinant production as SEQ ID NOs: 9 and 10 respectively.
However, Fab 3D3 was generated from recombinantly produced 3D3 by incubation with immobilized papain, followed by removal of the Fc fragment with immobilized protein A. Fab 3D3 was then purified by Superdex 200 size-exclusion chromatography in 10 mM Tris-HCl pH 8.0 and 150 mM NaCl.
For recombinant scFv 2D10, included in SEQ ID NO:10, a synthetic gene codon-optimized for Drosophila melanogaster encoding 2D10 heavy chain variable region, a (GGGGS)3GGG linker, and 2D10 light chain variable region, was cloned into pMT-puro in-frame with an N-terminal BiP signal sequence and a C-terminal thrombin cleavage site followed by a Twin-Strep purification tag. The resulting scFv 2D10 expression plasmid was used to obtain stably-transfected Schneider 2 (S2) insect cells. Secreted scFv 2D10 was affinity purified on a StrepTrap column, digested with thrombin protease to remove the purification tag, and then purified by Superdex 200 size-exclusion chromatography in 10 mM Tris-HCl pH 8.0 and 150 mM NaCl.
A synthetic gene encoding RSV G ectodomain (G[ecto]) P03423) was cloned into pCF in-frame with an N-terminal TPA signal sequence and C-terminal tandem 6-histidine and Twin-Strep purification tags (SEQ ID NO:7 that includes residues 64 to 298, UniProtKB entry). G[ecto] was produced by transient-transfection in CHO cells and secreted G[ecto] was affinity purified on a StrepTrap column.
A synthetic gene codon-optimized for Escherichia coli encoding RSV G residues 161 to 197 (G [161-197]) (SEQ ID NO:1 UniProtKB entry P03423) with a C-terminal 6-histidine purification tag (SEQ ID NO:8) was cloned into pET52b. The peptide was expressed overnight in E. coli BL21(DE3) at 18° C. The cells were then were lysed by ultrasonication in 20 mM Tris-HCl pH 8.0, 150 mM NaCl, and 25 mM imidazole (Buffer A) containing 2 μM MgCl2, benzonase, and protease inhibitors. RSV G[161-197] was purified from soluble lysates by HisTrap FF affinity chromatography and eluted with a gradient into Buffer B (Buffer A containing 500 mM imidazole). Analogous methods were used to produce related peptides (G [162-172] (SEQ ID NO: 2) and G [169-198] (SEQ ID NO: 3)).
Purified mAbs at a concentration of 5 μg/mL (150 μL total) were incubated overnight at room temperature in 96-well ELISA microtiter plates. Plates were then washed three times with PBS containing 0.05% Tween 20 (PBST). Wells were blocked by adding 150 μL of 5% BSA in PBS and incubating at room temperature for 1 hr followed by three PBST washes. Recombinant RSV G[ecto] at 5 μg/mL or RSV G[161-197] at 20 μg/mL in 1% BSA in PBS was serially diluted 1:3 with 1% BSA in PBS. Wells were incubated with 150 μL RSV G protein for 1 hr at room temperature and the plates were washed three times with PBST. The plates were then incubated for 1 hr at room temperature with 150 μL HRP-conjugated-HisProbe (ThermoFisher Scientific) diluted 1:5000 in 1% BSA in PBS. Plates were washed three times with PBST and developed by adding peroxidase substrate o-phenylenediamine dihydrochloride (OPD) in 0.05 M phosphate-citrate buffer pH 5.0 and 1.5% hydrogen peroxide for 10 min at room temperature. The reactions were stopped by incubation with 2N sulfuric acid for 10 min at room temperature, and the absorbance was measured at 490 nm. ELISA experiments were performed in biological triplicates.
The peptides, mutants and peptidomimetics of the invention are evaluated in a murine model using the following criteria.
An in vitro assay for RSV G modulation of CX3CR1 measures receptor mediated chemotaxis of human monocyte THP-1 cells {Tripp, R. A. et al. Nature Immunology (2001) 2:732-738}. In this assay, recombinant RSV G[161-197] induced chemotaxis at levels equivalent to the entire RSV G ectodomain, an activity blocked by pre-incubation with 3D3 or 2D10 or 3G12 at a level comparable to that provided by anti-CX3CR1 polyclonal serum. Table 2 provides the results of this analysis with respect to 3D3 and 2D10.
In more detail, the assay was performed using a transwell insert plate with an 8 μm pore size. Approximately 2 million log-phase THP-1 cells (a human leukemia monocytic cell line) washed twice and suspended in serum-free RPMI 1640 media were added to the upper chamber of the insert plate. Negative control was serum-free media alone to which serum-free media containing 25 nM mAb was added to the lower chamber. As a positive control, media containing 10% FBS was added to the lower chamber. RSV G[ecto] or RSV G[161-197] samples were added to the lower chamber at a final concentration of 5 nM in serum-free media. For samples with RSV G[161-197] and mAbs, RSV G[161-197] was pre-incubated with 5-molar excess mAb for 20 min at room temperature, and then added to serum-free media in the lower chamber, for a final concentration of 5 nM RSV G[161-197] and 25 nM mAb. For samples with anti-CX3CR1 antibody, 2 μL 1 mg/mL anti-CX3CR1 rabbit polyclonal antibody (ThermoFisher Scientific Cat# PAS-19910) was incubated with THP-1 cells for 30 minutes in the upper chamber before being placed into the well. The assembled plates were incubated in a CO2 incubator at 37° C. for 5 h. Cells migrated to the lower chamber were counted, and the chemotactic indices were determined by comparing the fold-increase in cell migration toward the chemoattractant to cell migration toward serum-free media alone. Experiments were performed in at least four biological replicates.
Formation and Structure Determination of the Fab 3D3-RSV G[162-172] Complex.
The synthetic peptide of Example 1B encoding RSV G amino acids 162 to 172 (UniProtKB entry P03423) (SEQ ID NO:2) was mixed in 5-molar excess with purified Fab 3D3 of Example 1A at 17.5 mg/ml in 10 mM Tris-HCl pH 8.0 and 150 mM NaCl. Crystals were grown by hanging drop vapor diffusion at 4° C. with a well solution of 23% PEG 3350 and 0.05 M zinc acetate. Crystals were transferred into a cryoprotectant solution of 26% PEG 3350, 0.05 M zinc acetate, and 25% ethylene glycol and flash frozen in liquid nitrogen. Diffraction data were collected at cryogenic temperature at the Advanced Light Source on beamline 8.3.1 using a wavelength of 1.11503 Å. Diffraction data from a single crystal were processed with iMosflm and Aimless. The Fab 3D3-RSV G[162-172] complex structure was solved by molecular replacement with a Fab homology model and the program PHASER, and the structure was refined and manually rebuilt using PHENIX and Coot, respectively. The final Fab 3D3-RSV G[162-172] complex structure (PDB code 5WNB) had the following Ramachandran statistics: 96.5% favored, 3.5% allowed, 0% outliers.
Formation and Structure Determination of the Fab 3D3-RSV G[161-197] Complex.
Purified RSV G[161-197] was mixed in 2 molar excess with purified Fab 3D3, dialyzed into 10 mM Tris-HCl pH 8.0 and 150 mM NaCl, and concentrated to 15 mg/mL. Crystals were grown by hanging drop vapor diffusion at 22° C. with a well solution of 21% PEG 3350 and 0.2 M ammonium citrate pH 7.0. Crystals were transferred into a cryoprotectant solution of 25% PEG 3350, 0.2 M ammonium citrate pH 7.0, and 25% glycerol and flash frozen in liquid nitrogen. Diffraction data were collected at cryogenic temperature at the Advanced Light Source beamline 8.3.1 using a wavelength of 1.11582 Å. Diffraction data were collected at cryogenic temperature at the Advanced Light Source on beamline 8.3.1 using a wavelength of 1.11503 Å. Diffraction data from a single crystal were processed with iMosflm and Aimless. The Fab 3D3-RSV G[161-197] complex structure was solved by molecular replacement with Fab 3D3 and the program PHASER, and the structure was refined and manually rebuilt using PHENIX and Coot, respectively. The final Fab 3D3-RSV G[161-197] complex structure (PDB code SWNA) had the following Ramachandran statistics: 97.6% favored, 2.4% allowed, 0% outliers.
Formation and Structure Determination of the scFv 2D10-RSV G[169-198] Complex.
A synthetic peptide encoding RSV G amino acids 169 to 198 (SEQ ID NO: 3) (UniProtKB entry P03423) was mixed in 2-molar excess with purified scFv in 60 mM Tris-HCl pH 8.0 and 230 mM NaCl and concentrated to 15.0 mg/mL. Crystals were grown by hanging drop vapor diffusion at 22° C. with a well solution of 24% PEG 4000, 0.17 M ammonium sulfate, 0.085 M sodium citrate pH 5.6 and 15% glycerol. Crystals were transferred into a cryoprotectant solution of 28% PEG 4000, 0.17 M ammonium sulfate, 0.085 M sodium citrate pH 5.6 and 15% glycerol, and 25% glycerol and flash frozen in liquid nitrogen. Diffraction data were collected at cryogenic temperature at the Advanced Photon Source on beamline 23-ID-D using a wavelength of 1.033 Å. Diffraction data from a single crystal were processed with HKL2000. The scFv 2D10-RSV G[169-198] complex structure was solved by molecular replacement with a scFv homology model and the program PHASER, and the structure was refined and manually rebuilt using PHENIX and Coot, respectively. The final scFv 2D10-RSV G[169-198] complex structure (PDB code 5WN9) had the following Ramachandran statistics: 99.2% favored, 0.8% allowed, 0% outliers.
Formation and Structure Determination of the Fab 3G12-RSV G[157-197] Complex.
Purified RSV G[157-197] was mixed in 2 molar excess with purified Fab 3G12 and the complex was purified on a Superdex200 size-exclusion column in 10 mM Tris-HCl pH 8.0 and 150 mM NaCl. The complex was concentrated to 15.0 mg/mL. Crystals were grown by hanging drop vapor diffusion at 22° C. with a well solution of 1.8 M ammonium sulfate and 100 mM sodium acetate trihydrate pH 4.4. Crystals were transferred into a cryoprotectant solution of 2.0 M ammonium sulfate, 100 mM sodium acetate trihydrate pH 4.4, and 25% glycerol and flash frozen in liquid nitrogen. Diffraction data were collected at cryogenic temperature at the Advanced Light Source on beamline 8.3.1 using a wavelength of 1.11582 Å. Diffraction data from a single crystal were processed with iMosflm and Aimless. The Fab 3G12+RSV G157-197 complex structure was solved by molecular replacement the program PHASER, and the structure was refined and manually rebuilt using PHENIX and Coot, respectively. The final Fab 3G12-RSV G[157-197] complex structure (PDB code 6MKC) had the following Ramachandran statistics: 95.7% favored, 4.3% allowed, 0% outliers.
Table 3 summarizes the crystallographic data (structures deposited in the Protein Data Bank: www.pdb.org).
aFor each structure, data from one crystal was used.
bValues in parentheses are for highest-resolution shell.
cRfree was calculated using 5% of data excluded from refinement.
Determination of structures of RSV G CCR protein in complex with the high affinity antibodies 2D10 and 3D3 shown in
As shown, each of these mutations shows diminished chemotactic activity, the most effective being the substitution of arginine for serine at position 177. Combinations of these mutations are included within the scope of the invention.
Chemically synthesized peptide technology, aided by combinatorial chemistry methods for synthesis and assay, now constitutes a mature technology for creating epitope mimics, with new advances enabling construction and screening of very large libraries (billions of compounds) by using DNA tags and next generation sequencing to deconvolute the hits {Chan, A. I., et al. Curr Opin Chem Biol. (2015) 26: 55-61}. For example, helical conformations can be stabilized through the insertion of amino acids with restricted conformational space, such as alpha-methylated amino acids (e.g. Aib), by side-chain cross-linking or ‘stapling’ to stabilize helical epitopes, and by the use of helix caps and hydrogen-bond surrogates. Examples include hydrazone crosslinks as hydrogen bond surrogates, Freidinger-like lactams and pseudoprolines to stabilize turns {Estieu-Gionnet, K. and Guichard, G. Exp. Opin. Drug Discov. (2011) 6: 937-963}.
Further, techniques known in the art for in vitro translation of mRNA into protein allow introduction of non-standard amino acids into proteins and peptides, facilitating formation of crosslinked peptides {Hartman, M. C., et al. PLoS One (2007) 2(10):e972}.
The peptides, mutants and peptidomimetics of the invention can be used to identify effective non-immunoglobulin binding agents.
A variety of non-immunoglobulin protein scaffolds is known in the art that provide equivalent pharmacological activity arising from high affinity, high specificity binding to an epitope similar to one bound by a traditional mAb {Sha, F, et al. Protein Sci. (2017) 26(5):910-924}. Examples include scaffolds based on fibronectin, lipocalin, lens crystallin, tetranectin, ankyrin, Protein A (Ig binding domain). Small peptide families may also have antibody-like affinity and specificity, including avian pancreatic peptides and conotoxins {Josephson, K., et al., J. Am. Chem. Soc. (2005) 127:11727-11725}. Cross-linked peptides similarly provide the ability to generate high affinity binding agents with well-defined specificity. In addition, non-protein based agents such as nucleic acid aptamers can also provide equivalent binding {Sun, H. and Zu, Y. Molecules (2015) 20(7):11959-80}.
In the table below, for the listed sequences that state that they include “plus additions” are those wherein the coding sequence of interest is supplemented by aids to expression and/or purification, such as a start codon, a glycine spacer, a histidine tag, or other purification aid such as Twin-Strep {Schmidt, T. G., et al. Protein Expr Purif. (2013) 92(1):54-61}. These are provided in more detail in the sequence listing that follows.
LENGTH: 37 amino acids
FEATURE: Immunogen recognized by mAbs 3D3, 2D10 and 3G12
OTHER INFORMATION: RSV G protein [residues 161-197]
LENGTH: 11 amino acids
FEATURE: Immunogen recognized by mAb 3D3 but not mAb 2D10
OTHER INFORMATION: RSV G protein [residues 162-172]
LENGTH: 30 amino acids
FEATURE: Immunogen recognized by mAb 2D10 but not mAb 3D3
OTHER INFORMATION: RSV G protein [residues 169-198]
LENGTH: 50 amino acids
FEATURE: Immunogen recognized by mAbs 3D3, 2D10, and 3G12
OTHER INFORMATION: RSV G protein [residues 157-197]
LENGTH: 45 amino acids
FEATURE: Immunogen recognized by mAbs Please include
OTHER INFORMATION: RSV G protein [residues 148-197]
LENGTH: 39 amino acids
FEATURE: Immunogen recognized by mAbs Please include
OTHER INFORMATION: RSV G protein [residues 161-195]
LENGTH: 295 amino acids
OTHER INFORMATION: RSV G protein ectodomain [residues 64-298 from RSV strain A2,
GenBank KT992094.1, with 2 synonymous mutatations (underlined)] with N terminal TPA
secretion signal and C terminal 6His-2Strep tag
MDAMKRGLCCVLLLCGAVFVSPSEFSANHKVTPTTAIIQDATSQIKNTTP
DNA sequence:
ATGGACGCCATGAAGCGGGGCCTGTGCTGTGTGCTGCTGCTGTGCGGAGC
CGTGTTCGTGTCCCCCAGCGAATTCTCGGCAAACCACAAAGTCACACCAA
TTGGAGTCATCCACAATTCGAGAAGGGCGGCGGCTCCGGAGGTGGATCAG
GAGGTGGTTCCTGGTCACACCCTCAATTCGAGAAGTGA
LENGTH: 45 amino acids
OTHER INFORMATION: RSV G protein [residues 161-197] with N terminal start codon and spacer glycine and C terminal 6His tag
MGNDFHFEVFNFVPCSICSNNPTCWAICKRIPNKKPGKKHHHHHH
DNA sequence:
ATGGGAAACGACTTCCACTTCGAGGTGTTCAACTTCGTTCCGTGCAGCAT
LENGTH: 54 amino acids
OTHER INFORMATION: RSV G protein [residues 157-197] with N terminal start codon and spacer glycine and C terminal 6His tag
MGSKPNNDFHFEVFNFVPCSICSNNPTCWAICKRIPNKKPGKKHHHHHH
DNA sequence:
ATGGGAAGCAAACCGAACAACGACTTCCACTTCGAGGTGTTCAACTTCGT
LENGTH: 45 amino acids
OTHER INFORMATION: RSV G protein [residues 148-197] with N terminal start codon and spacer glycine and C terminal 6His tag
MGTKQRQNKSKPNNDFHFEVFNFVPCSICSNNPTCWAICKRIPNKKPGKK
HHHHHH
DNA sequence:
ATGGGAACCAAGCAGCGTCAGAACAAGCCGCCGAGCAAACCGAACAACGA
LENGTH: 39 amino acids
OTHER INFORMATION: RSV G protein [residues 161-195] with N terminal start codon and spacer glycine and C terminal 6His tag
MGNDFHFEVFNFVPCSICSNNPTCWAICKRIPNHHHHHH
DNA sequence:
ATGGGAAACGACTTCCACTTCGAGGTGTTCAACTTCGTTCCGTGCAGCAT
LENGTH: 308 amino acids
FEATURE: Single-chain antibody
OTHER INFORMATION: mAb 3D3 single chain Fv (scFv 3D3) with N terminal Bip signal sequence, internal flexible linker and C terminal thrombin protease cleavage site followed by 6His-2Strep tag
MKLCILLAVVAFVGLSLGRSEEQLVESGGGLVQPGRSLRLSCVGSGLRFE
GGGSGGGGSQIVLTQSPATLSLSPGERATLSCRASQSVSNHLAWYQQKPG
EK
DNA seauence:
ATGAAGTTATGCATATTACTGGCCGTCGTGGCCTTTGTTGGCCTCTCGCT
CGGGAGATCTGAAGAGCAACTGGTGGAGAGCGGTGGTGGTCTGGTTCAGC
GGTGGCGGTAGCGGTGGCGGTGGCAGCCAGATTGTGCTGACCCAGAGCCC
CCTGGTTCCCCGCGGATCGGGTTGGAGTCATCCACAATTCGAGAAGGGCG
GCGGCTCCGGAGGTGGATCAGGAGGTGGTTCCTGGTCACACCCTCAATTC
GAGAAGTGA
LENGTH: 315 amino acids
FEATURE: Single-chain antibody
OTHER INFORMATION: mAb 2D10 single chain Fv (scFv 2D10) with N terminal Bip signal sequence, internal flexible linker and C terminal thrombin protease cleavage site followed by 6His-2Strep tag
MKLCILLAVVAFVGLSLGRSQVQLVQSGPEVKKPGASVRLSCKASGYVFT
SGGGGSGGGGSGGGDTPMTQSPSSVSASVGDRVTISCRASQGISNSLAWY
SWSHPQFEK
DNA sequence:
ATGAAGTTATGCATATTACTGGCCGTCGTGGCCTTTGTTGGCCTCTCGCT
CGGGAGATCTCAGGTGCAGCTGGTGCAGAGCGGCCCGGAAGTGAAAAAGC
TCTGGTGGCGGCGGTAGCGGTGGTGGCGGTAGCGGCGGCGGTGACACCCC
ATCCACAATTCGAGAAGGGCGGCGGCTCCGGAGGTGGATCAGGAGGTGGT
TCCTGGTCACACCCTCAATTCGAGAAGTGA
Included in the invention are the following embodiments:
1. A peptide having the amino acid sequence of residues 161-197 of respiratory syncytial virus (RSV) G protein (SEQ ID NO:1) or the amino acid sequence of positions 162-172 (SEQ ID NO:2) or of positions 169-198 (SEQ ID NO:3), or of positions 157-197 (SEQ ID NO:4), or of positions 148-197 (SEQ ID NO:5), or of positions 161-195 (SEQ ID NO:6) each chemically stabilized to retain the conformation exhibited upon binding to antibody.
2. The peptide above wherein said chemical stabilizing comprises providing covalent crosslinking.
3. A mutant or peptidomimetic of the peptide of any one of SEQ ID NOs:1-6 that has enhanced immunogenicity as compared to the respective peptide of any one of SEQ ID NOs:1-6.
4. The mutant or peptidomimetic above which is a mutant comprising no more than five amino acid substitutions and/or deletions and/or additions.
5. A mutant described in embodiment 3 or 4 wherein the conformation of said mutant is chemically stabilized.
6. A mutant or peptidomimetic of the peptide of any one of SEQ ID NOs:1-6 that has reduced immunogenicity as compared to the respective peptide of SEQ ID NOs:1-6.
7. The mutant or peptidomimetic above which is a mutant comprising no more than five amino acid substitutions and/or deletions and/or additions that has altered pharmacological activity with respect to activation of the chemokine receptor responsive to fractalkine.
8. A mutant described above in embodiment 6 or 7 wherein the conformation of said mutant is chemically stabilized.
9. A molecule having desirable properties as an immunogen, wherein said properties include induction of antibodies that have strain independent high affinity for the conserved region of the RSV G protein and have neutralizing activity, that is identified by contacting a candidate molecule with the mAb 3D3, 2D10 or 3G12 or an antigen-binding fragment thereof and with at least one binding moiety that binds with low affinity to the RSV G protein, whereby a candidate molecule that preferentially binds to 3D3, 2D10, 3G12 or fragment is identified as having said desirable properties as an immunogen.
10. The molecule described above wherein the candidate molecule is an aptamer or a member of a combinatorial library of small molecules or of peptides.
11. A molecule that comprises covalently linked components wherein said components are peptides of the amino acid sequence SEQ ID NO:2 and the amino acid sequence of SEQ ID NO:3 or each of said components is the corresponding mutant or peptidomimetic of SEQ ID NO:2 and/or SEQ ID NO:3 as described in embodiments 3-8.
12. A mutant or peptidomimetic of peptides of SEQ ID NO:1 or SEQ ID NOs:3-6 that stimulates or inhibits the chemokine receptor responsive to fractalkine.
13. The mutant or peptidomimetic above that has reduced immunogenicity as compared to the respective peptide of SEQ ID NO:1 or SEQ ID NOs:3-6.
14. A mutant peptide comprising the amino acid sequence of SEQ ID NO:1 or SEQ ID NOs:3-6 which contains at least one substitution for amino acid 162, 164, 166, 177, 187, 192 and/or of 193 the RSV G protein which mutant shows reduced chemotactic activity as compared to wild type RSV G protein.
15. A method to design a mutant peptide for use as a vaccine against RSV which method comprises identifying amino acids that are contained within the CCR of the G protein which amino acids do not participate in the binding of high affinity antibodies and substituting for them amino acids with side chains of different shape or size or charge, thus inhibiting the binding of the mutant to the receptor (CX3CR1) without interfering with the immunogenicity of the peptide or protein.
16. A mutant designed by the method above in embodiment 15.
17. A peptide or mutant peptide described in any of the preceding embodiments coupled to moiety for use in assay of said peptide or mutant or for use in purification of said peptide or mutant.
18. A pharmaceutical or veterinary composition comprising as active ingredient at least one of any peptide, peptidomimetic, mutant or molecule described above.
19. A method to provide a prophylactic or therapeutic treatment with respect to RSV infection in a subject which method comprises administering to a subject in need of such treatment an effective amount of the pharmaceutical composition just described.
20. A method to treat immune mediated inflammatory diseases, chronic pain and peripheral neuropathy which method comprises administering to a subject in need of such treatment an effective amount of the pharmaceutical or veterinary composition wherein the active agent is that described in embodiments 12 or 13.
21. The method of above wherein the condition is rheumatoid arthritis, osteoarthritis or atherosclerosis.
22. A recombinant expression system for the production of any peptides or mutants described above which expression system is a nucleic acid that comprises a nucleotide sequence encoding said peptide or mutant operably linked to control sequences for its expression.
23. Recombinant host cells modified to produce any peptide or mutant described in the embodiments above.
24. A method to produce a peptide or mutant that binds an antibody immunoreactive with the G protein of RSV or a conserved region thereof or that has altered activity with respect to the receptor that binds fractalkine which method comprises culturing these cells under conditions whereby said peptide or mutant is produced and optionally recovering said peptide or mutant from said culture.
25. A method to identify a molecule having desirable properties as an immunogen, wherein said properties include induction of antibodies that have strain independent high affinity for the conserved region of the RSV G protein and have neutralizing activity, which method comprises contacting a candidate molecule with the mAb 3D3, 2D10 or 3G12 or an antigen-binding fragment thereof and with at least one binding moiety that binds with low affinity to the RSV G protein, whereby a candidate molecule that preferentially binds to 3D3, 2D10 or 3G12 is identified as having said desirable properties as an immunogen.
26. The method above wherein the candidate molecule is an aptamer or a member of a combinatorial library of small molecules or of peptides.
27. A method to identify a binding moiety that has the characteristics of strain independent high affinity for the conserved region of the RSV G protein and neutralizing activity which method comprises contacting a candidate binding moiety with a conformationally restrained form of a peptide having the shape as shown in
28. The method above wherein the candidate binding moiety is an aptamer or a member of a combinatorial library of alternative scaffolds or is an antibody or fragment thereof.
29. A binding moiety identified by this method.
30. A pharmaceutical or veterinary composition comprising as active ingredient the binding moiety above.
31. A method to provide a prophylactic or therapeutic treatment with respect to RSV infection in a subject which method comprises administering to a subject in need of such treatment an effective amount of this pharmaceutical or veterinary composition.
This application claims benefit of U.S. Application Ser. No. 62/572,271 filed 13 Oct. 2017, U.S. Application Ser. No. 62/588,022 filed 17 Nov. 2017 and U.S. Application Ser. No. 62/633,999 filed 22 Feb. 2018. The contents of the above patent applications are incorporated by reference herein in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62633999 | Feb 2018 | US | |
| 62588022 | Nov 2017 | US | |
| 62572271 | Oct 2017 | US |
