Broadly Neutralizing Antibodies Present New Prospects to Counter Highly Antigenically Diverse Viruses

被引:347
作者
Burton, Dennis R. [1 ,2 ,3 ,4 ]
Poignard, Pascal [1 ,2 ,7 ]
Stanfield, Robyn L. [5 ,6 ]
Wilson, Ian A. [5 ,6 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Int AIDS Vaccine Initiat IAVI Neutralizing Antibo, La Jolla, CA 92037 USA
[3] Massachusetts Gen Hosp, MIT, Ragon Inst, Boston, MA 02129 USA
[4] Harvard Univ, Boston, MA 02129 USA
[5] Scripps Res Inst, Skaggs Inst Chem Biol, Dept Mol Biol, La Jolla, CA 92037 USA
[6] Scripps Res Inst, IAVI Neutralizing Antibody Ctr, La Jolla, CA 92037 USA
[7] IAVI, New York, NY 10038 USA
关键词
HEPATITIS-C VIRUS; HUMAN MONOCLONAL-ANTIBODIES; INFLUENZA-A VIRUSES; MEMORY B-CELLS; STRUCTURAL BASIS; RATIONAL DESIGN; ENVELOPE GLYCOPROTEIN; E2; GLYCOPROTEIN; HIV-1; EPITOPE;
D O I
10.1126/science.1225416
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
Certain human pathogens avoid elimination by our immune system by rapidly mutating the surface protein sites targeted by antibody responses, and consequently they tend to be problematic for vaccine development. The behavior described is prominent for a subset of viruses-the highly antigenically diverse viruses-which include HIV, influenza, and hepatitis C viruses. However, these viruses do harbor highly conserved exposed sites, usually associated with function, which can be targeted by broadly neutralizing antibodies. Until recently, not many such antibodies were known, but advances in the field have enabled increasing numbers to be identified. Molecular characterizations of the antibodies and, most importantly, of the sites of vulnerability that they recognize give hope for the discovery of new vaccines and drugs.
引用
收藏
页码:183 / 186
页数:4
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