Virus attachment and replication are promoted after acquisition of host CD28 and CD152 by HIV-1

J Infect Dis. 2005 Oct 1;192(7):1265-8. doi: 10.1086/444426. Epub 2005 Aug 25.

Abstract

CD28 is constitutively expressed on CD4(+) cells, but its homologue CD152 is only weakly expressed after cell activation. To determine whether these 2 costimulatory molecules can be inserted into human immunodeficiency virus type 1 (HIV-1), virus was produced in CD28- and CD152-expressing Jurkat-derived cells. Both molecules were efficiently acquired by virions. Virus attachment and infectivity were more affected by CD152 than by CD28. Given that CD28/CD152-CD80/CD86 interactions play a dominant role in antigen presentation, it can thus be proposed that the association between virus-anchored host CD28/CD152 and cell-surface CD80/CD86 on target cells might have consequences for the transmission and pathogenesis of HIV-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD
  • Antigens, Differentiation / metabolism*
  • CD28 Antigens / metabolism*
  • CTLA-4 Antigen
  • Down-Regulation*
  • HIV-1 / metabolism
  • HIV-1 / pathogenicity*
  • HIV-1 / physiology*
  • Humans
  • Jurkat Cells
  • Up-Regulation*
  • Virion / metabolism

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • CD28 Antigens
  • CTLA-4 Antigen
  • CTLA4 protein, human