Identification of a novel CD4i human monoclonal antibody Fab that neutralizes HIV-1 primary isolates from different clades

被引:21
作者
Zhang, MY
Shu, Y
Sidorov, I
Dimitrov, DS [1 ]
机构
[1] NCI, Human Immunovirol & Computat Biol Grp, LECB, CCR,NIH, Frederick, MD 21702 USA
[2] NCI, BRP, SAIC Frederick Inc, Frederick, MD 21702 USA
关键词
HIV; antibody; phage display; gp120; inhibitors; vaccines;
D O I
10.1016/j.antiviral.2003.09.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A new human monoclonal antibody (hmAb), designated m 16, was selected by sequential antigen panning (SAP) of a human phage display library against recombinant soluble HIV-1 envelope glycoproteins (Envs) (gp140s) and their complexes with soluble CD4. It bound with high (nM) affinity to gp120 and gp140; the binding was further enhanced by interactions of the Envs with CD4. m16 inhibited cell fusion mediated by the Envs of 9 HIV-1 isolates from clades A, B, E and G with potency on average comparable to that of the broadly neutralizing human monoclonal antibody Fab X5. The identification of a new hmAb with broad neutralizing activity that exhibits differential inhibitory profile suggests a potential for its use as a component of anti-HIV-1 treatments. Published by Elsevier B.V.
引用
收藏
页码:161 / 164
页数:4
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