Rational antibody-based HIV-1 vaccine design: current approaches and future directions

被引:167
作者
Walker, Laura M. [1 ,2 ]
Burton, Dennis R. [1 ,2 ,3 ,4 ]
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] MIT, Massachusetts Gen Hosp, Ragon Inst, Boston, MA 02114 USA
[4] Harvard, Boston, MA 02114 USA
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; NEUTRALIZING MONOCLONAL-ANTIBODIES; POLYVALENT DNA PRIME; ENVELOPE GLYCOPROTEIN; IN-VITRO; CELL REPERTOIRE; RHESUS MACAQUES; SHIV CHALLENGE; CHIMERIC VIRUS; TYPE-1; VACCINE;
D O I
10.1016/j.coi.2010.02.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Many antiviral vaccines elicit neutralizing antibodies as a correlate of protection. For HIV, given the huge variability of the virus, it is widely believed that the induction of a broadly neutralizing antibody (bNAb) response will be crucial in a successful vaccine against the virus. Unfortunately, despite many efforts, the development of an immunogen that elicits bNAbs remains elusive. However, recent structural studies of HIV-1 Env proteins, generation of novel bNAbs, maturation of technologies for the isolation of further antibodies, insights into the requirements for antibody-mediated protection, and novel vaccination approaches are providing grounds for renewed optimism.
引用
收藏
页码:358 / 366
页数:9
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