作者
Nicole A Doria-Rose, Jinal N Bhiman, Ryan S Roark, Chaim A Schramm, Jason Gorman, Gwo-Yu Chuang, Marie Pancera, Evan M Cale, Michael J Ernandes, Mark K Louder, Mangaiarkarasi Asokan, Robert T Bailer, Aliaksandr Druz, Isabella R Fraschilla, Nigel J Garrett, Marissa Jarosinski, Rebecca M Lynch, Krisha McKee, Sijy O'Dell, Amarendra Pegu, Stephen D Schmidt, Ryan P Staupe, Matthew S Sutton, Keyun Wang, Constantinos Kurt Wibmer, Barton F Haynes, Salim Abdool-Karim, Lawrence Shapiro, Peter D Kwong, Penny L Moore, Lynn Morris, John R Mascola
发表日期
2016/1/1
期刊
Journal of virology
卷号
90
期号
1
页码范围
76-91
出版商
American Society for Microbiology
简介
The epitopes defined by HIV-1 broadly neutralizing antibodies (bNAbs) are valuable templates for vaccine design, and studies of the immunological development of these antibodies are providing insights for vaccination strategies. In addition, the most potent and broadly reactive of these bNAbs have potential for clinical use. We previously described a family of 12 V1V2-directed neutralizing antibodies, CAP256-VRC26, isolated from an HIV-1 clade C-infected donor at years 1, 2, and 4 of infection (N. A. Doria-Rose et al., Nature 509:55–62, 2014, http://dx.doi.org/10.1038/nature13036). Here, we report on the isolation and characterization of new members of the family mostly obtained at time points of peak serum neutralization breadth and potency. Thirteen antibodies were isolated from B cell culture, and eight were isolated using trimeric envelope probes for differential single B cell sorting. One of the new …
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