A Blueprint for HIV Vaccine Discovery

被引:310
作者
Burton, Dennis R. [1 ,2 ,13 ,14 ,16 ]
Ahmed, Rafi [5 ,16 ]
Barouch, Dan H. [6 ,13 ,14 ,16 ]
Butera, Salvatore T. [1 ,16 ]
Crotty, Shane [7 ,16 ]
Godzik, Adam [8 ,16 ]
Kaufmann, Daniel E. [13 ,14 ,16 ]
McElrath, M. Juliana [9 ,16 ]
Nussenzweig, Michel C. [10 ,11 ,16 ]
Pulendran, Bali [5 ,16 ]
Scanlan, Chris N. [12 ,16 ]
Schief, William R. [1 ,2 ,16 ]
Silvestri, Guido [5 ,15 ,16 ]
Streeck, Hendrik [13 ,14 ]
Walker, Bruce D. [13 ,14 ,16 ]
Walker, Laura M. [1 ]
Ward, Andrew B. [3 ,4 ,16 ]
Wilson, Ian A. [3 ,4 ,16 ]
Wyatt, Richard [1 ,2 ,16 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[2] Scripps Res Inst, IAVI Neutralizing Antibody Ctr, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[4] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[5] Emory Univ, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[6] Beth Israel Deaconess Med Ctr, Div Vaccine Res, Boston, MA 02215 USA
[7] La Jolla Inst Allergy & Immunol, Div Vaccine Discovery, La Jolla, CA 92037 USA
[8] Sanford Burnham Med Res Inst, Grad Sch Biomed Sci, La Jolla, CA 92037 USA
[9] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98109 USA
[10] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10065 USA
[11] Rockefeller Univ, Lab Mol Immunol, New York, NY 10065 USA
[12] Univ Oxford, Dept Biochem, Oxford Glycobiol Inst, Oxford OX1 3QU, England
[13] MIT, Massachusetts Gen Hosp, Ragon Inst, Boston, MA 02114 USA
[14] Harvard Univ, Boston, MA 02114 USA
[15] Emory Univ, Yerkes Natl Primate Res Ctr, Atlanta, GA 30329 USA
[16] Scripps Res Inst, Scripps Ctr HIV AIDS Vaccine Immunol & Immunogen, La Jolla, CA 92037 USA
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; T FOLLICULAR HELPER; AUTOLOGOUS NEUTRALIZING ANTIBODY; HUMAN MONOCLONAL-ANTIBODIES; SITE-SPECIFIC ANALYSIS; CD4; BINDING-SITE; ENVELOPE GLYCOPROTEINS; STRUCTURAL BASIS; B-CELLS; BROAD NEUTRALIZATION;
D O I
10.1016/j.chom.2012.09.008
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite numerous attempts over many years to develop an HIV vaccine based on classical strategies, none has convincingly succeeded to date. A number of approaches are being pursued in the field, including building upon possible efficacy indicated by the recent RV144 clinical trial, which combined two HIV vaccines. Here, we argue for an approach based, in part, on understanding the HIV envelope spike and its interaction with broadly neutralizing antibodies (bnAbs) at the molecular level and using this understanding to design immunogens as possible vaccines. BnAbs can protect against virus challenge in animal models, and many such antibodies have been isolated recently. We further propose that studies focused on how best to provide T cell help to B cells that produce bnAbs are crucial for optimal immunization strategies. The synthesis of rational immunogen design and immunization strategies, together with iterative improvements, offers great promise for advancing toward an HIV vaccine.
引用
收藏
页码:396 / 407
页数:12
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