4.6 Article

Capacity for Infectious HIV-1 Virion Capture Differs by Envelope Antibody Specificity

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JOURNAL OF VIROLOGY
卷 88, 期 9, 页码 5165-5170

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AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.03765-13

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资金

  1. National Institutes of Health (NIH/NIAID/DAIDS) Center for HIV/AIDS Vaccine Immunology [U01 AI067854]
  2. CHAVI-ID [AI100645]
  3. Hope [PO1AI082971]
  4. Bill and Melinda Gates Foundation Collaboration for AIDS Vaccine Discovery grant [Haynes OPP 1033098]
  5. Global Health Grant [Hope OPP1031734]
  6. HIV-1 Vaccine Trials Network (HVTN) [5U01 AI46725-05]
  7. Duke University Center for AIDS Research (CFAR) [P30 AI 64518]

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Antibody capacity to recognize infectious virus is a prerequisite of many antiviral functions. We determined the infectious virion capture index (IVCI) of different antibody specificities. Whereas broadly neutralizing antibodies (bNAbs), except for an MPER bNAb, selectively captured infectious virions, non-bNAbs and mucosal human immunodeficiency virus type 1 (HIV-1)-positive IgG captured subsets of both infectious and noninfectious virions. Infectious virion capture was additive with a mixture of antibodies, providing proof of concept for vaccine-induced antibodies that together have improved capacity to recognize infectious virions.

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