Role of immune mechanisms in induction of HIV-1 broadly neutralizing antibodies

被引:81
作者
Verkoczy, Laurent [1 ,2 ,3 ]
Kelsoe, Garnett [2 ,4 ]
Moody, M. Anthony [1 ,5 ]
Haynes, Barton F. [2 ,3 ,4 ]
机构
[1] Duke Univ, Med Ctr, Duke Human Vaccine Inst, Durham, NC 27708 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Immunol, Durham, NC USA
[5] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; PRE-B-CELL; PROXIMAL EXTERNAL REGION; COMPLEMENTARITY-DETERMINING REGION; HUMAN MONOCLONAL-ANTIBODIES; HEAVY-CHAIN; SHIV CHALLENGE; GP41; MEMBRANE; GLYCOPROTEIN;
D O I
10.1016/j.coi.2011.04.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although antibodies can be elicited by HIV-1 infection or immunization, those that are broadly neutralizing (bnAbs) are undetectable in most individuals, and when they do arise in HIV-1 infection, only do so years after transmission. Until recently, the reasons for difficulty in inducing such bnAbs have been obscure. Recent technological advances in isolating bnAbs from rare patients have increased our knowledge of their specificities and features, and along with gene-targeting studies, have also begun uncovering evidence of immunoregulatory roadblocks preventing their induction. One crucial avenue towards developing an effective HIV-1 vaccine is to harness this emerging information into the rational design of immunogens and formulation of adjuvants, such that structural and immunological hurdles to routinely eliciting bnAbs can be overcome.
引用
收藏
页码:383 / 390
页数:8
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