Induction of a virus-specific effector-memory CD4+ T cell response by attenuated SIV infection

Marie Claire Gauduin, Yi Yu, Amy Barabasz, Angela Carville, Mike Piatak, Jeffrey D. Lifson, Ronald C. Desrosiers, R. Paul Johnson

Research output: Contribution to journalArticlepeer-review

58 Scopus citations


We investigated simian immunodeficiency virus (SIV)-specific CD4 + T cell responses in rhesus macaques chronically infected with attenuated or pathogenic SIV strains. Analysis of SIVΔnef-infected animals revealed a relatively high frequency of SIV-specific CD4+ T cells representing 4-10% of all CD4+ T lymphocytes directed against multiple SIV proteins. Gag-specific CD4+ T cells in wild-type SIV-infected animals were 5-10-fold lower in frequency and inversely correlated with the level of plasma viremia. SIV-specific CD4+ cells from SIVΔnef animals were predominantly CD27-CD28 -CD45RAlowCCR7-CCR5-, consistent with an effector-memory subset, and included a fully differentiated CD45RA +CCR7- subpopulation. In contrast, SIV-specific CD4 + T cells from SIV-infected animals were mostly CD27+C D28+CD45RA-CCR7+CCR5+, consistent with an early central memory phenotype. The CD45RA+CCR7 -CD4+ subset from SIVΔnef animals was highly enriched for effector CD4+ T cells, as indicated by the perforin expression and up-regulation of the lysosomal membrane protein CD107a after SIV Gag stimulation. SIV-specific CD4+ T cells in attenuated SIV-infected animals were increased in frequency in bronchioalveolar lavage and decreased in lymph nodes, consistent with an effector-memory T cell population. The ability of SIVΔnef to induce a high frequency virus-specific CD4+ T cell response with direct effector function may play a key role in protective immunity produced by vaccination with attenuated SIV strains.

Original languageEnglish (US)
Pages (from-to)2661-2672
Number of pages12
JournalJournal of Experimental Medicine
Issue number12
StatePublished - Nov 2006
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)


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