作者
Rebecca M Lynch, Eli Boritz, Emily E Coates, Adam DeZure, Patrick Madden, Pamela Costner, Mary E Enama, Sarah Plummer, Lasonji Holman, Cynthia S Hendel, Ingelise Gordon, Joseph Casazza, Michelle Conan-Cibotti, Stephen A Migueles, Randall Tressler, Robert T Bailer, Adrian McDermott, Sandeep Narpala, Sijy O’Dell, Gideon Wolf, Jeffrey D Lifson, Brandie A Freemire, Robert J Gorelick, Janardan P Pandey, Sarumathi Mohan, Nicolas Chomont, Remi Fromentin, Tae-Wook Chun, Anthony S Fauci, Richard M Schwartz, Richard A Koup, Daniel C Douek, Zonghui Hu, Edmund Capparelli, Barney S Graham, John R Mascola, Julie E Ledgerwood, VRC 601 Study Team
发表日期
2015/12/23
期刊
Science translational medicine
卷号
7
期号
319
页码范围
319ra206-319ra206
出版商
American Association for the Advancement of Science
简介
Passive immunization with HIV-1–neutralizing monoclonal antibodies (mAbs) is being considered for prevention and treatment of HIV-1 infection. As therapeutic agents, mAbs could be used to suppress active virus replication, maintain suppression induced by antiretroviral therapy (ART), and/or decrease the size of the persistent virus reservoir. We assessed the impact of VRC01, a potent human mAb targeting the HIV-1 CD4 binding site, on ART-treated and untreated HIV-1–infected subjects. Among six ART-treated individuals with undetectable plasma viremia, two infusions of VRC01 did not reduce the peripheral blood cell–associated virus reservoir measured 4 weeks after the second infusion. In contrast, six of eight ART-untreated, viremic subjects infused with a single dose of VRC01 experienced a 1.1 to 1.8 log10 reduction in plasma viremia. The two subjects with minimal responses to VRC01 were found to …
引用总数
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