Lewitus Eric, Sanders-Buell Eric, Bose Meera, O'Sullivan Anne Marie, Poltavee Kultida, Li Yifan, Bai Hongjun, Mdluli Thembi, Donofrio Gina, Slike Bonnie, Zhao Hong, Wong Kim, Chen Lennie, Miller Shana, Lee Jenica, Ahani Bahar, Lepore Steven, Muhammad Sevan, Grande Rebecca, Tran Ursula, Dussupt Vincent, Mendez-Rivera Letzibeth, Nitayaphan Sorachai, Kaewkungwal Jaranit, Pitisuttithum Punnee, Rerks-Ngarm Supachai, O'Connell Robert J, Janes Holly, Gilbert Peter B, Gramzinski Robert, Vasan Sandhya, Robb Merlin L, Michael Nelson L, Krebs Shelly J, Herbeck Joshua T, Edlefsen Paul T, Mullins James I, Kim Jerome H, Tovanabutra Sodsai, Rolland Morgane
US Military HIV Research Program, WRAIR, Silver Spring, MD 20910, USA.
Department of Microbiology, University of Washington, Seattle, WA 98195, USA.
Virus Evol. 2021 Jul 9;7(2):veab057. doi: 10.1093/ve/veab057. eCollection 2021.
The scale of the HIV-1 epidemic underscores the need for a vaccine. The multitude of circulating HIV-1 strains together with HIV-1's high evolvability hints that HIV-1 could adapt to a future vaccine. Here, we wanted to investigate the effect of vaccination on the evolution of the virus post-breakthrough infection. We analyzed 2,635 HIV-1 sequences sampled up to a year post-diagnosis from 110 vaccine and placebo participants who became infected in the RV144 vaccine efficacy trial. We showed that the Env signature sites that were previously identified to distinguish vaccine and placebo participants were maintained over time. In addition, fewer sites were under diversifying selection in the vaccine group than in the placebo group. These results indicate that HIV-1 would possibly adapt to a vaccine upon its roll-out.
HIV-1 疫情的规模凸显了疫苗的必要性。众多循环的 HIV-1 毒株以及 HIV-1 的高进化能力表明,HIV-1 可能会适应未来的疫苗。在此,我们想要研究疫苗接种对突破感染后病毒进化的影响。我们分析了在 RV144 疫苗疗效试验中感染的 110 名疫苗接种者和安慰剂组参与者在诊断后长达一年时间内采集的 2635 条 HIV-1 序列。我们发现,先前确定的用于区分疫苗接种者和安慰剂组参与者的 Env 特征位点随时间保持不变。此外,与安慰剂组相比,疫苗组中处于多样化选择下的位点更少。这些结果表明,HIV-1 在疫苗推出后可能会适应疫苗。