Proof of principle for epitope-focused vaccine design

被引:407
作者
Correia, Bruno E. [1 ,2 ,3 ,4 ]
Bates, John T. [5 ]
Loomis, Rebecca J. [6 ]
Baneyx, Gretchen [1 ]
Carrico, Chris [7 ]
Jardine, Joseph G. [1 ,8 ,9 ,10 ]
Rupert, Peter [7 ]
Correnti, Colin [7 ]
Kalyuzhniy, Oleksandr [1 ,9 ,10 ]
Vittal, Vinayak [1 ]
Connell, Mary J. [6 ]
Stevens, Eric [1 ]
Schroeter, Alexandria [1 ]
Chen, Man [11 ]
MacPherson, Skye [1 ,8 ,9 ,10 ]
Serra, Andreia M. [1 ,8 ,9 ,10 ]
Adachi, Yumiko [1 ,9 ,10 ]
Holmes, Margaret A.
Li, Yuxing [8 ,9 ,10 ]
Klevit, Rachel E. [1 ]
Graham, Barney S. [11 ]
Wyatt, Richard T. [8 ,9 ,10 ]
Baker, David [1 ]
Strong, Roland K. [7 ]
Crowe, James E., Jr. [5 ,12 ,13 ]
Johnson, Philip R. [6 ]
Schief, William R. [1 ,8 ,9 ,10 ]
机构
[1] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[2] Univ Nova Lisboa, Inst Gulbenkian Ciencia, PhD Program Computat Biol, P-2780157 Oeiras, Portugal
[3] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2780157 Oeiras, Portugal
[4] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
[5] Vanderbilt Univ, Vanderbilt Vaccine Ctr, Med Ctr, Nashville, TN 37232 USA
[6] Childrens Hosp Philadelphia, Res Inst, Philadelphia, PA 19104 USA
[7] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
[8] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[9] Scripps Res Inst, IAVI Neutralizing Antibody Ctr, La Jolla, CA 92037 USA
[10] Scripps Res Inst, Ctr HIV AIDS Vaccine Immunol & Immunogen Discover, La Jolla, CA 92037 USA
[11] NIAID, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
[12] Vanderbilt Univ Sch Med, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA
[13] Vanderbilt Univ Sch Med, Dept Pediat, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
SYNCYTIAL VIRUS RSV; NEUTRALIZING ANTIBODY; COMPUTATIONAL DESIGN; PROTEIN; INFECTION; MOTAVIZUMAB; INDUCTION; SCAFFOLDS; PROGRAM; BURDEN;
D O I
10.1038/nature12966
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Vaccines prevent infectious disease largely by inducing protective neutralizing antibodies against vulnerable epitopes. Several major pathogens have resisted traditional vaccine development, although vulnerable epitopes targeted by neutralizing antibodies have been identified for several such cases. Hence, new vaccine design methods to induce epitope-specific neutralizing antibodies are needed. Here we show, with a neutralization epitope from respiratory syncytial virus, that computational protein design can generate small, thermally and conformationally stable protein scaffolds that accurately mimic the viral epitope structure and induce potent neutralizing antibodies. These scaffolds represent promising leads for the research and development of a human respiratory syncytial virus vaccine needed to protect infants, young children and the elderly. More generally, the results provide proof of principle for epitope-focused and scaffold-based vaccine design, and encourage the evaluation and further development of these strategies for a variety of other vaccine targets, including antigenically highly variable pathogens such as human immunodeficiency virus and influenza.
引用
收藏
页码:201 / 206
页数:6
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