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Neutralizing monoclonal antibodies block human immunodeficiency virus type 1 infection of dendritic cells and transmission to T cells

  • Sarah S. Frankel*
  • , Ralph M. Steinman
  • , Nelson L. Michael
  • , Silvia Ratto Kim
  • , Nina Bhardwaj
  • , Melissa Pope
  • , Mark K. Louder
  • , Philip K. Ehrenberg
  • , Paul W.H.I. Parren
  • , Dennis R. Burton
  • , Hermann Katinger
  • , Thomas C. Vancott
  • , Merlin Robb
  • , Deborah L. Birx
  • , John R. Mascola
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

83 Scopus citations

Abstract

Prevention of the initial infection of mucosal dendritic cells (DC) and interruption of the subsequent transmission of HIV-1 from DC to T cells are likely to be important attributes of an effective human immunodeficiency virus type 1 (HIV-1) vaccine. While anti-HIV-1 neutralizing antibodies have been difficult to elicit by immunization, there are several human monoclonal antibodies (MAbs) that effectively neutralize virus infection of activated T cells. We investigated the ability of three well-characterized neutralizing MAbs (IgG1b12, 2F5, and 2G12) to block HIV-1 infection of human DC. DC were generated from CD14+ blood cells or obtained from cadaveric human skin. The MAbs prevented viral entry into purified DC and the ensuing productive infection in DC/T-cell cultures. When DC were first pulsed with HIV-1, MAbs blocked the subsequent transmission to unstimulated CD3+ T cells. Thus, neutralizing antibodies can block HIV-1 infection of DC and the cell-to-cell transmission of virus from infected DC to T cells. These data suggest that neutralizing antibodies could interrupt the initial events associated with mucosal transmission and regional spread of HIV-1.

Original languageEnglish
Pages (from-to)9788-9794
Number of pages7
JournalJournal of Virology
Volume72
Issue number12
DOIs
StatePublished - Dec 1998

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