Antigen-driven C–C Chemokine-mediated HIV-1 Suppression by CD4+ T Cells from Exposed Uninfected Individuals Expressing the Wild-type CCR-5 Allele

نویسندگان

  • Lucinda Furci
  • Gabriella Scarlatti
  • Samuele Burastero
  • Giuseppe Tambussi
  • Claudia Colognesi
  • Caroline Quillent
  • Renato Longhi
  • Patrizia Loverro
  • Barbara Borgonovo
  • Davide Gaffi
  • Emily Carrow
  • Mauro Malnati
  • Paolo Lusso
  • Antonio G. Siccardi
  • Adriano Lazzarin
  • Alberto Beretta
چکیده

Despite repeated exposure to HIV-1, certain individuals remain persistently uninfected. Such exposed uninfected (EU) people show evidence of HIV-1-specific T cell immunity and, in rare cases, selective resistance to infection by macrophage-tropic strains of HIV-1. The latter has been associated with a 32-base pair deletion in the C-C chemokine receptor gene CCR-5, the major coreceptor of macrophage-tropic strains of HIV-1. We have undertaken an analysis of the HIV-specific T cell responses in 12 EU individuals who were either homozygous for the wild-type CCR-5 allele or heterozygous for the deletion allele (CCR-5Delta32). We have found evidence of an oligoclonal T cell response mediated by helper T cells specific for a conserved region of the HIV-1 envelope. These cells produce very high levels of C-C chemokines when stimulated by the specific antigen and suppress selectively the replication of macrophage-tropic, but not T cell-tropic, strains of HIV-1. These chemokine-producing helper cells may be part of a protective immune response that could be potentially exploited for vaccine development.

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عنوان ژورنال:
  • The Journal of Experimental Medicine

دوره 186  شماره 

صفحات  -

تاریخ انتشار 1997