LFA-1 expression on target cells promotes human immunodeficiency virus type 1 infection and transmission

J Virol. 2001 Jan;75(2):1077-82. doi: 10.1128/JVI.75.2.1077-1082.2001.

Abstract

While CD4 and the chemokine receptors are the principal receptors for human immunodeficiency virus (HIV), other cellular proteins, such as LFA-1, are also involved in HIV infection. LFA-1 and its ligands, ICAM-1, ICAM-2, and ICAM-3, can be expressed on the cells infected by HIV, as well as on the HIV virions themselves. To examine the role of LFA-1 expressed on target cells in HIV infection, Jurkat-derived Jbeta2.7 T-cell lines that express either wild-type LFA-1, a constitutively active mutant LFA-1, or no LFA-1 were used. The presence of wild-type LFA-1 enhanced the initial processes of HIV infection, as well as the subsequent replication and transmission from cell to cell. In contrast, the constitutively active LFA-1 mutant failed to promote virus replication and spread, even though this mutant could help HIV enter cells and establish the initial infection. This study clearly demonstrates the contribution of LFA-1 in the different stages of HIV infection. Moreover, not only is LFA-1 expression important for initial HIV-cell interaction, subsequent replication, and transmission, but its activity must also be properly regulated.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Adhesion
  • HIV-1 / physiology*
  • Humans
  • Jurkat Cells
  • Ligands
  • Lymphocyte Function-Associated Antigen-1 / genetics
  • Lymphocyte Function-Associated Antigen-1 / metabolism*
  • Lymphocyte Function-Associated Antigen-1 / pharmacology
  • Mutation
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes / virology*
  • Virus Replication

Substances

  • Ligands
  • Lymphocyte Function-Associated Antigen-1