Neutralizing antibodies generated during natural HIV-1 infection: good news for an HIV-1 vaccine?

被引:350
作者
Stamatatos, Leonidas [1 ,2 ]
Morris, Lynn [3 ,4 ]
Burton, Dennis R. [5 ,6 ]
Mascola, John R. [7 ]
机构
[1] Seattle Biomed Res Inst, Seattle, WA 98109 USA
[2] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[3] Natl Inst Communicable Dis, AIDS Virus Res Unit, Johannesburg, South Africa
[4] Ctr AIDS Programme Res S Africa, Johannesburg, South Africa
[5] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[6] Scripps Res Inst, Int AIDS Vaccine Initiat Neutralizing Antibody Ct, La Jolla, CA 92037 USA
[7] NIAID, Vaccine Res Ctr, US Natl Inst Hlth, Bethesda, MD 20892 USA
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; MONOCLONAL-ANTIBODIES; CHIMERIC VIRUS; ENV CLONES; GLYCOPROTEIN; PROTECTION; MACAQUES; SUBTYPES; SEROTYPES; RESPONSES;
D O I
10.1038/nm.1949
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most existing viral vaccines generate antibodies that either block initial infection or help eradicate the virus before it can cause disease. For HIV-1, obstacles to eliciting protective neutralizing antibodies (NAbs) have often seemed insurmountable. The target of HIV-specific NAbs, the viral envelope glycoprotein (Env), is highly variable in amino acid sequence and glycosylation pattern. Conserved elements of HIV-1 Env seem to be poorly immunogenic, and previous attempts to generate broadly reactive NAbs by vaccination have proven ineffective. However, recent studies show that in the sera of some HIV-1-infected individuals can neutralize diverse HIV-1 isolates. Detailed analyses of these sera provide new insights into the viral epitopes targeted by broadly reactive NAbs. The findings discussed here suggest that the natural NAb response to HIV-1 can inform future vaccine design. A concerted effort of structure-based vaccine design will help guide the development of improved antibody-based vaccines for HIV-1.
引用
收藏
页码:866 / 870
页数:5
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