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Prevention efficacy of the broadly neutralizing antibody VRC01 depends on HIV-1 envelope sequence features.

Michal Juraska | Hongjun Bai | Allan C deCamp | Craig A Magaret | Li Li | Kevin Gillespie | Lindsay N Carpp | Elena E Giorgi | James Ludwig | Cindy Molitor | Aaron Hudson | Brian D Williamson | Nicole Espy | Brian Simpkins | Erika Rudnicki | Danica Shao | Raabya Rossenkhan | Paul T Edlefsen | Dylan H Westfall | Wenjie Deng | Lennie Chen | Hong Zhao | Tanmoy Bhattacharya | Alec Pankow | Ben Murrell | Anna Yssel | David Matten | Talita York | Nicolas Beaume | Asanda Gwashu-Nyangiwe | Nonkululeko Ndabambi | Ruwayhida Thebus | Shelly T Karuna | Lynn Morris | David C Montefiori | John A Hural | Myron S Cohen | Lawrence Corey | Morgane Rolland | Peter B Gilbert | Carolyn Williamson | James I Mullins
Proceedings of the National Academy of Sciences of the United States of America | 2024

In the Antibody Mediated Prevention (AMP) trials (HVTN 704/HPTN 085 and HVTN 703/HPTN 081), prevention efficacy (PE) of the monoclonal broadly neutralizing antibody (bnAb) VRC01 (vs. placebo) against HIV-1 acquisition diagnosis varied according to the HIV-1 Envelope (Env) neutralization sensitivity to VRC01, as measured by 80% inhibitory concentration (IC80). Here, we performed a genotypic sieve analysis, a complementary approach to gaining insight into correlates of protection that assesses how PE varies with HIV-1 sequence features. We analyzed HIV-1 Env amino acid (AA) sequences from the earliest available HIV-1 RNA-positive plasma samples from AMP participants diagnosed with HIV-1 and identified Env sequence features that associated with PE. The strongest Env AA sequence correlate in both trials was VRC01 epitope distance that quantifies the divergence of the VRC01 epitope in an acquired HIV-1 isolate from the VRC01 epitope of reference HIV-1 strains that were most sensitive to VRC01-mediated neutralization. In HVTN 704/HPTN 085, the Env sequence-based predicted probability that VRC01 IC80 against the acquired isolate exceeded 1 µg/mL also significantly associated with PE. In HVTN 703/HPTN 081, a physicochemical-weighted Hamming distance across 50 VRC01 binding-associated Env AA positions of the acquired isolate from the most VRC01-sensitive HIV-1 strain significantly associated with PE. These results suggest that incorporating mutation scoring by BLOSUM62 and weighting by the strength of interactions at AA positions in the epitope:VRC01 interface can optimize performance of an Env sequence-based biomarker of VRC01 prevention efficacy. Future work could determine whether these results extend to other bnAbs and bnAb combinations.

Pubmed ID: 38241441

Research resources used in this publication

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: R37 AI054165
  • Agency: NIH HHS, United States
    Id: S10 OD028685
  • Agency: NIAID NIH HHS, United States
    Id: UM1 AI068614
  • Agency: NIAID NIH HHS, United States
    Id: UM1 AI068635

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CATNAP (tool)

RRID:SCR_016170

Analyze a database of HIV-1 IC50 and IC80 neutralization data from publicly-available sources, in conjunction with HIV-1 Envelope sequences. Access to an extensive databases of information about neutralizing antibodies and viruses used in published neutralization studies. Tool interfaces also allow input and analysis of user data. PMID: 26044712

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