In Vivo gp41 Antibodies Targeting the 2F5 Monoclonal Antibody Epitope Mediate Human Immunodeficiency Virus Type 1 Neutralization Breadth

被引:92
|
作者
Shen, Xiaoying [1 ,2 ]
Parks, Robert J. [1 ,4 ]
Montefiori, David C. [1 ,2 ]
Kirchherr, Jennifer L. [1 ,4 ]
Keele, Brandon F. [6 ]
Decker, Julie M. [6 ]
Blattner, William A. [5 ]
Gao, Feng [1 ,4 ]
Weinhold, Kent J. [1 ,2 ,3 ]
Hicks, Charles B. [4 ]
Greenberg, Michael L. [2 ]
Hahn, Beatrice H. [6 ]
Shaw, George M. [6 ]
Haynes, Barton F. [1 ,3 ,4 ]
Tomaras, Georgia D. [1 ,2 ,3 ]
机构
[1] Duke Univ, Med Ctr, Duke Human Vaccine Inst, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[5] Univ Maryland, Inst Human Virol, Div Epidemiol & Prevent, Baltimore, MD 21201 USA
[6] Univ Alabama, Dept Med, Birmingham, AL 35294 USA
关键词
PROXIMAL EXTERNAL REGION; HIV-1; INFECTION; SURFACE-ANTIGEN; 4E10; RESPONSES; PROTEINS; ENVELOPE; SITE; 2G12;
D O I
10.1128/JVI.02631-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The broadly neutralizing human monoclonal antibodies (MAbs) 2F5 and 4E10, both targeting the highly conserved human immunodeficiency virus type 1 (HIV-1) envelope membrane proximal external region (MPER), are among the MAbs with the broadest heterologous neutralizing activity and are of considerable interest for HIV-1 vaccine development. We have identified serum antibodies from an HIV-infected subject that both were broadly neutralizing and specifically targeted MPER epitopes that overlap the 2F5 epitope. These MPER-specific antibodies were made 15 to 20 months following transmission and concomitantly with the development of autoantibodies. Our findings suggest that multiple events (i.e., genetic predisposition and HIV-1 immune dysregulation) may be required for induction of broadly reactive gp41 MPER antibodies in natural infection.
引用
收藏
页码:3617 / 3625
页数:9
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