HIV-1 envelope trimer elicits more potent neutralizing antibody responses than monomeric gp120

被引:136
作者
Kovacs, James M. [2 ,3 ]
Nkolola, Joseph P. [1 ,4 ]
Peng, Hanqin [2 ]
Cheung, Ann [1 ]
Perry, James [1 ]
Miller, Caroline A. [1 ]
Seaman, Michael S. [1 ]
Barouch, Dan H. [1 ,4 ]
Chen, Bing [2 ,3 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Vaccine Res, Boston, MA 02215 USA
[2] Childrens Hosp, Div Mol Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[4] Ragon Inst MGH MIT & Harvard, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; HUMAN MONOCLONAL-ANTIBODY; PROTECTIVE EFFICACY; GP41; ECTODOMAIN; GLYCOPROTEIN; VACCINE; GP140; BROAD; EPITOPE; IMMUNOGENICITY;
D O I
10.1073/pnas.1204533109
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
HIV-1 envelope glycoprotein is the primary target for HIV-1-specific antibodies. The native HIV-1 envelope spike on the virion surface is a trimer, but trimeric gp140 and monomeric gp120 currently are believed to induce comparable immune responses. Indeed, most studies on the immunogenicity of HIV-1 envelope oligomers have revealed only marginal improvement over monomers. We report here that suitably prepared envelope trimers have nearly all the antigenic properties expected for native viral spikes. These stable, rigorously homogenous trimers have antigenic properties markedly different from those of monomeric gp120s derived from the same sequences, and they induce potent neutralizing antibody responses for a cross-clade set of tier 1 and tier 2 viruses with titers substantially higher than those elicited by the corresponding gp120 monomers. These results, which demonstrate that there are relevant immunologic differences between monomers and high-quality envelope trimers, have important implications for HIV-1 vaccine development.
引用
收藏
页码:12111 / 12116
页数:6
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