HIV-1 replication increases HIV-specific CD4+ T cell frequencies but limits proliferative capacity in chronically infected children

Zachary A. Scott, Coreen M. Beaumier, Mark Sharkey, Mario Stevenson, Katherine Luzuriaga

Research output: Contribution to journalArticlepeer-review

21 Scopus citations


This study investigated the relationship between HIV-1 replication and virus (HIV-1; CMV)-specific CD4+ T cell frequency and function in HIV-1-infected children. HIV-1 gag p55-specific CD4+ T cell IFN-γ responses were detected in the majority of children studied. p55-specific responses were detected less commonly and at lower frequencies in children with <50 copies/ml plasma HIV-1 RNA than in children with active HIV-1 replication. In children with <50 copies/ml plasma HIV-1, p55-specific responses were detected only in children with evidence of ongoing HIV-1 replication, indicating a direct relationship between HIV-1 replication and HIV-specific CD4+ T cell frequencies. In contrast, p55-specific proliferative responses were detected more frequently in children with <50 copies/ml plasma HIV-1. CMV-specific CD4+ responses were more commonly detected and at higher frequencies in CMV-coinfected children with suppressed HIV-1 replication. The lack of HIV-specific CD4+ proliferative responses, along with the preservation of CMV-specific CD4+ responses in children with controlled HIV-1 replication, suggests that viral replication may have deleterious effects on HIV-1 and other virus-specific CD4+ responses. Vaccination to stimulate HIV-specific CD4+ T cell responses in these children may synergize with antiretroviral therapy to improve the long-term control of viral replication, and may perhaps allow the eventual discontinuation of antiretroviral therapy.

Original languageEnglish (US)
Pages (from-to)5786-5792
Number of pages7
JournalJournal of Immunology
Issue number11
StatePublished - Jun 1 2003
Externally publishedYes

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology


Dive into the research topics of 'HIV-1 replication increases HIV-specific CD4<sup>+</sup> T cell frequencies but limits proliferative capacity in chronically infected children'. Together they form a unique fingerprint.

Cite this