Fc receptor but not complement binding is important in antibody protection against HIV

被引:0
|
作者
Ann J. Hessell
Lars Hangartner
Meredith Hunter
Carin E. G. Havenith
Frank J. Beurskens
Joost M. Bakker
Caroline M. S. Lanigan
Gary Landucci
Donald N. Forthal
Paul W. H. I. Parren
Preston A. Marx
Dennis R. Burton
机构
[1] The Scripps Research Institute,Departments of Immunology and Molecular Biology
[2] La Jolla,Division of Infectious Diseases, Department of Medicine
[3] California 92037,undefined
[4] USA,undefined
[5] Tulane National Primate Research Center,undefined
[6] Tulane University,undefined
[7] Covington,undefined
[8] Louisiana 70433,undefined
[9] USA,undefined
[10] Genmab,undefined
[11] University of California,undefined
[12] Irvine School of Medicine,undefined
[13] Irvine,undefined
[14] California 92697,undefined
[15] USA,undefined
来源
Nature | 2007年 / 449卷
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学科分类号
摘要
Many effective vaccines act by inducing neutralizing antibodies, and this approach is a top priority in work on HIV vaccines. But a new study suggests that anti-HIV antibodies are most effective when they act in two ways: through neutralization — killing the virus outright and blocking its entry into T cells — and by killing infected cells. The use of engineered versions of a neutralizing human antibody that protects against HIV in a monkey model shows that protection is dependent not only the antibody's neutralizing activity, but also on its interaction with Fc receptors on effector cells, which may act to reduce virus yield from infected cells. This work suggests that the best results might be achieved with vaccines that recruit both neutralizing antibodies and cell-mediated immunity via agents such as macrophages and cytokinins, rather than antibodies.
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页码:101 / 104
页数:3
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