Worldwide Distribution of HIV Type 1 Epitopes Recognized by Human Anti-V3 Monoclonal Antibodies

被引:25
|
作者
Cardozo, Timothy [1 ,2 ]
Swetnam, James [2 ]
Pinter, Abraham [3 ]
Krachmarov, Chavdar [3 ]
Nadas, Arthur [2 ]
Almond, David [2 ]
Zolla-Pazner, Susan [2 ,4 ]
机构
[1] NYU, Med Ctr, Sch Med, Dept Pharmacol, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Pathol & Environm Med, New York, NY 10016 USA
[3] Univ Med & Dent New Jersey, Publ Hlth Res Inst, Newark, NJ 07107 USA
[4] New York VA Med Ctr, New York, NY 10010 USA
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; GENETIC SUBTYPES; NEUTRALIZATION; PEPTIDES; PROTEINS; BINDING; GP120;
D O I
10.1089/aid.2008.0188
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epitopes, also known as antigenic determinants, are small clusters of specific atoms within macromolecules that are recognized by the immune system. Such epitopes can be targeted with vaccines designed to protect against specific pathogens. The third variable loop (V3 loop) of the HIV-1 pathogen's gp120 surface envelope glycoprotein can be a highly sensitive neutralization target. We derived sequence motifs for the V3 loop epitopes recognized by the human monoclonal antibodies (mAbs) 447-52D and 2219. Searching the HIV database for the occurrence of each epitope motif in worldwide viruses and correcting the results based on published WHO epidemiology reveal that the 447-52D epitope we defined occurs in 13% of viruses infecting patients worldwide: 79% of subtype B viruses, 1% of subtype C viruses, and 7% of subtype A/AG sequences. In contrast, the epitope we characterized for human anti-V3 mAb 2219 is present in 30% of worldwide isolates but is evenly distributed across the known HIV-1 subtypes: 48% of subtype B strains, 40% of subtype C, and 18% of subtype A/AG. Various assays confirmed that the epitopes corresponding to these motifs, when expressed in the SF162 Env backbone, were sensitively and specifically neutralized by the respective mAbs. The method described here is capable of accurately determining the worldwide occurrence and subtype distribution of any crystallographically resolved HIV-1 epitope recognized by a neutralizing antibody, which could be useful for multivalent vaccine design. More importantly, these calculations demonstrate that globally relevant, structurally conserved epitopes are present in the sequence variable V3 loop.
引用
收藏
页码:441 / 450
页数:10
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