comparative magnitude of cross-strain conservation of hiv variable loop neutralization epitopes的比较级cross-strain hiv守恒变量循环中和抗原表位.pdfVIP

Comparative Magnitude of Cross-Strain Conservation of HIV Variable Loop Neutralization Epitopes 1 1 2,3 1 James Swetnam , Evgeny Shmelkov , Susan Zolla-Pazner , Timothy Cardozo * 1 Department of Pharmacology, New York University School of Medicine, New York, New York, United States of America, 2 Department of Pathology, New York University School of Medicine, New York, New York, United States of America, 3 New York Veterans Affairs Medical Center, New York, New York, United States of America Abstract Although the sequence variable loops of the human immunodeficiency virus’ (HIV-1) surface envelope glycoprotein (gp120) can exhibit good immunogenicity, characterizing conserved (invariant) cross-strain neutralization epitopes within these loops has proven difficult. We recently developed a method to derive sensitive and specific signature motifs for the three- dimensional (3D) shapes of the HIV-1 neutralization epitopes in the third variable (V3) loop of gp120 that are recognized by human monoclonal antibodies (mAbs). We used the signature motif method to estimate the conservation of these epitopes across circulating worldwide HIV-1 strains. The epitope targeted by the anti-V3 loop neutralizing mAb 3074 is present in 87% of circulating strains, distributed nearly evenly among all subtypes. The results for other anti-V3 Abs are: 3791, present in 63% of primarily non-B subtypes; 2219, present in 56% of strains across all subtypes; 2557, present in 52% across all subtypes; 447-52D, present in 11% of primarily subtype B strains; 537-10D, present in 9% of primarily subtype B strains; and 268-D, present in 5% of primarily subtype B strains. The estimates correlate with in vitro tests of these mAbs against diverse