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Anti-V3 Monoclonal Antibodies Display Broad Neutralizing Activities against Multiple HIV-1 Subtypes

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  • Catarina E Hioe
  • Terri Wrin
  • Michael S Seaman
  • Xuesong Yu
  • Blake Wood
  • Steve Self
  • Constance Williams
  • Miroslaw K Gorny
  • Susan Zolla-Pazner

Abstract

Background: The V3 loop of the HIV-1 envelope (Env) glycoprotein gp120 was identified as the “principal neutralizing domain” of HIV-1, but has been considered too variable to serve as a neutralizing antibody (Ab) target. Structural and immunochemical data suggest, however, that V3 contains conserved elements which explain its role in binding to virus co-receptors despite its sequence variability. Despite this evidence of V3 conservation, the ability of anti-V3 Abs to neutralize a significant proportion of HIV-1 isolates from different subtypes (clades) has remained controversial. Methods: HIV-1 neutralization experiments were conducted in two independent laboratories to test human anti-V3 monoclonal Abs (mAbs) against pseudoviruses (psVs) expressing Envs of diverse HIV-1 subtypes from subjects with acute and chronic infections. Neutralization was defined by 50% inhibitory concentrations (IC50), and was statistically assessed based on the area under the neutralization titration curves (AUC). Results: Using AUC analyses, statistically significant neutralization was observed by ≥1 anti-V3 mAbs against 56/98 (57%) psVs expressing Envs of diverse subtypes, including subtypes A, AG, B, C and D. Even when the 10 Tier 1 psVs tested were excluded from the analysis, significant neutralization was detected by ≥1 anti-V3 mAbs against 46/88 (52%) psVs from diverse HIV-1 subtypes. Furthermore, 9/24 (37.5%) Tier 2 viruses from the clade B and C standard reference panels were neutralized by ≥1 anti-V3 mAbs. Each anti-V3 mAb tested was able to neutralize 28–42% of the psVs tested. By IC50 criteria, 40/98 (41%) psVs were neutralized by ≥1 anti-V3 mAbs. Conclusions: Using standard and new statistical methods of data analysis, 6/7 anti-V3 human mAbs displayed cross-clade neutralizing activity and revealed that a significant proportion of viruses can be neutralized by anti-V3 Abs. The new statistical method for analysis of neutralization data provides many advantages to previously used analyses.

Suggested Citation

  • Catarina E Hioe & Terri Wrin & Michael S Seaman & Xuesong Yu & Blake Wood & Steve Self & Constance Williams & Miroslaw K Gorny & Susan Zolla-Pazner, 2010. "Anti-V3 Monoclonal Antibodies Display Broad Neutralizing Activities against Multiple HIV-1 Subtypes," PLOS ONE, Public Library of Science, vol. 5(4), pages 1-14, April.
  • Handle: RePEc:plo:pone00:0010254
    DOI: 10.1371/journal.pone.0010254
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    1. Peter D. Kwong & Michael L. Doyle & David J. Casper & Claudia Cicala & Stephanie A. Leavitt & Shahzad Majeed & Tavis D. Steenbeke & Miro Venturi & Irwin Chaiken & Michael Fung & Hermann Katinger & Pau, 2002. "HIV-1 evades antibody-mediated neutralization through conformational masking of receptor-binding sites," Nature, Nature, vol. 420(6916), pages 678-682, December.
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    1. Ziyang Xu & Susanne Walker & Megan C. Wise & Neethu Chokkalingam & Mansi Purwar & Alan Moore & Edgar Tello-Ruiz & Yuanhan Wu & Sonali Majumdar & Kylie M. Konrath & Abhijeet Kulkarni & Nicholas J. Turs, 2022. "Induction of tier-2 neutralizing antibodies in mice with a DNA-encoded HIV envelope native like trimer," Nature Communications, Nature, vol. 13(1), pages 1-18, December.

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