Multidonor Analysis Reveals Structural Elements, Genetic Determinants, and Maturation Pathway for HIV-1 Neutralization by VRC01-Class Antibodies

被引:290
作者
Zhou, Tongqing [1 ]
Zhu, Jiang [1 ]
Wu, Xueling [1 ]
Moquin, Stephanie [1 ]
Zhang, Baoshan [1 ]
Acharya, Priyamvada [1 ]
Georgiev, Ivelin S. [1 ]
Altae-Tran, Han R. [1 ]
Chuang, Gwo-Yu [1 ]
Joyce, M. Gordon [1 ]
Do Kwon, Young [1 ]
Longo, Nancy S. [1 ]
Louder, Mark K. [1 ]
Luongo, Timothy [1 ]
McKee, Krisha [1 ]
Schramm, Chaim A. [5 ]
Skinner, Jeff [2 ]
Yang, Yongping [1 ]
Yang, Zhongjia [1 ]
Zhang, Zhenhai [5 ]
Zheng, Anqi [1 ]
Bonsignori, Mattia [6 ,7 ]
Haynes, Barton F. [6 ,7 ]
Scheid, Johannes F. [8 ]
Nussenzweig, Michel C. [8 ,9 ]
Simek, Melissa [10 ]
Burton, Dennis R. [11 ,12 ,13 ,14 ]
Koff, Wayne C. [10 ]
Mullikin, James C. [4 ]
Connors, Mark [3 ]
Shapiro, Lawrence [1 ,5 ]
Nabel, Gary J. [1 ]
Mascola, John R. [1 ]
Kwong, Peter D. [1 ]
机构
[1] NIAID, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
[2] NIAID, Bioinformat & Computat Biosci Branch, Off Cyber Infrastruct & Computat Biol, NIH, Bethesda, MD 20892 USA
[3] NIAID, Lab Immunoregulat, NIH, Bethesda, MD 20892 USA
[4] NHGRI, NIH Intramural Sequencing Ctr, NIH, Bethesda, MD 20892 USA
[5] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[6] Duke Univ, Sch Med, Duke Human Vaccine Inst, Durham, NC 27710 USA
[7] Duke Univ, Med Ctr, Durham, NC 27710 USA
[8] Rockefeller Univ, Lab Mol Immunol, New York, NY 10065 USA
[9] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10065 USA
[10] Int AIDS Vaccine Initiat, New York, NY 10038 USA
[11] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[12] Scripps Res Inst, IAVI Neutralizing Antibody Ctr, La Jolla, CA 92037 USA
[13] Scripps Res Inst, Ctr HIV AIDS Vaccine Immunol & Immunogen Design, La Jolla, CA 92037 USA
[14] Ragon Inst MGH MIT & Harvard, Cambridge, MA 02129 USA
基金
美国国家卫生研究院;
关键词
VACCINE EFFICACY; CD4-BINDING SITE; BINDING-SITE; VIRUS; BROAD; ENVELOPE; PROTEIN; PROTECTION; EVOLUTION; SEQUENCE;
D O I
10.1016/j.immuni.2013.04.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antibodies of the VRC01 class neutralize HIV-1, arise in diverse HIV-1-infected donors, and are potential templates for an effective HIV-1 vaccine. However, the stochastic processes that generate repertoires in each individual of >10(12) antibodies make elicitation of specific antibodies uncertain. Here we determine the ontogeny of the VRC01 class by crystallography and next-generation sequencing. Despite antibody-sequence differences exceeding 50%, antibody-gp120 cocrystal structures reveal VRC01-class recognition to be remarkably similar. B cell transcripts indicate that VRC01-class antibodies require few specific genetic elements, suggesting that naive-B cells with VRC01-class features are generated regularly by recombination. Virtually all of these fail to mature, however, with only a few-likely one-ancestor B cell expanding to form a VRC01-class lineage in each donor. Developmental similarities in multiple donors thus reveal the generation of VRC01-class antibodies to be reproducible in principle, thereby providing a framework for attempts to elicit similar antibodies in the general population.
引用
收藏
页码:245 / 258
页数:14
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