2026-05-11 ロックフェラー大学
＜関連情報＞
- https://www.rockefeller.edu/news/39559-hiv-broadly-neutralizing-antibodies-mutations-disease-therapies/
- https://www.nature.com/articles/s41564-026-02347-x
HIV-1株における広範中和抗体回避への多様な経路 Diverse paths to broadly neutralizing antibody escape among HIV-1 strains
Alex C. Stabell,Songhee Lee,Debby J. Park,Christy L. Lavine,Sebastian Mejia Espinosa,Viren A. Baharani,Rachel Patejak,Michel C. Nussenzweig,Marina Caskey,Michael S. Seaman,Paul D. Bieniasz & Theodora Hatziioannou
Nature Microbiology Published:11 May 2026
DOI:https://doi.org/10.1038/s41564-026-02347-x
Abstract
Broadly neutralizing antibodies (bnAbs) are promising agents for HIV-1 treatment and prevention. However, the genetic barriers and mutational pathways to viral resistance, which can limit therapeutic antibody utility, remain poorly defined. Here we developed a medium-to-high throughput approach to determine the mutations that confer resistance to neutralization by the bnAbs 3BNC117 and 10-1074 currently in clinical development. We performed 7,776 parallel selection experiments to identify bnAb resistance mutations in 15 primary isolates that span global HIV-1 genetic diversity. There was substantial variability among HIV-1 isolates in the identity of mutations that conferred bnAb resistance. For 12 of 15 HIV-1 isolates, single amino acid changes could increase bnAb IC80 to >10 μg ml−1. Some 3BNC117 resistance mutations conferred resistance to additional bnAbs targeting the same or different epitopes, and unconventional escape mechanisms were occasionally encountered. These data provide a rationale for selecting bnAb combinations that are most likely to achieve treatment success.
