4.7 Article

Incomplete Neutralization and Deviation from Sigmoidal Neutralization Curves for HIV Broadly Neutralizing Monoclonal Antibodies

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PLOS PATHOGENS
卷 11, 期 8, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.ppat.1005110

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资金

  1. International AIDS Vaccine Initiative through the Neutralizing Antibody Consortium [SFP1849]
  2. National Institutes of Allergy and Infectious Diseases, [R01 AI033292]
  3. Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery Grant [UM1AI100663]
  4. Ragon Institute of MGH, MIT
  5. Bill and Melinda Gates Foundation as part of the Collaboration for AIDS Vaccine Discovery [1032144]
  6. Vici grant from The Netherlands Organization for Scientific Research [918.66.628]
  7. European Community's Sixth Framework Program 'European HIV Enterprise (EUROPRISE)' (FP6) [037611]
  8. European Community's Seventh Framework Program 'Next-Generation HIV-1 Immunogens Inducing Broadly Reactive Neutralizing Antibodies (NGIN)' (FP7) [201433]
  9. Aids fonds Netherlands [2012041]
  10. Vidi grant from the Netherlands Organization for Scientific Research [917.11.314]
  11. European Research Council [ERC-StG- 2011-280829-SHEV]
  12. Harvard Training Program
  13. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [UM1AI100663, R01AI033292] Funding Source: NIH RePORTER

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The broadly neutralizing HIV monoclonal antibodies (bnMAbs) PG9, PG16, PGT151, and PGT152 have been shown earlier to occasionally display an unusual virus neutralization profile with a non-sigmoidal slope and a plateau at <100% neutralization. In the current study, we were interested in determining the extent of non-sigmoidal slopes and plateaus at <100% for HIV bnMAbs more generally. Using both a 278 panel of pseudoviruses in a CD4 T-cell (U87.CCR5.CXCR4) assay and a panel of 117 viruses in the TZM-bl assay, we found that bnMAbs targeting many neutralizing epitopes of the spike had neutralization profiles for at least one virus that plateaued at <90%. Across both panels the bnMAbs targeting the V2 apex of Env and gp41 were most likely to show neutralization curves that plateaued <100%. Conversely, bnMAbs targeting the high-mannose patch epitopes were less likely to show such behavior. Two CD4 binding site (CD4bs) Abs also showed this behavior relatively infrequently. The phenomenon of incomplete neutralization was also observed in a large peripheral blood mononuclear cells (PBMC)-grown molecular virus clone panel derived from patient viral swarms. In addition, five bnMAbs were compared against an 18-virus panel of molecular clones produced in 293T cells and PBMCs and assayed in TZM-bl cells. Examples of plateaus <90% were seen with both types of virus production with no consistent patterns observed. In conclusion, incomplete neutralization and non-sigmoidal neutralization curves are possible for all HIV bnMAbs against a wide range of viruses produced and assayed in both cell lines and primary cells with implications for the use of antibodies in therapy and as tools for vaccine design.

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