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Circulating rotavirus-specific T cells have a poor functional profile

  • Miguel Parra
  • , Daniel Herrera
  • , María Fernanda Jácome
  • , Martha C. Mesa
  • , Luz Stella Rodríguez
  • , Carolina Guzmán
  • , Juana Angel
  • , Manuel A. Franco
  • Universidad Javeriana

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Frequencies of circulating T cells producing IFN-γ, TNF-α, and IL-2, and percentages of T cells proliferating after stimulation with rotavirus (RV), tetanus toxoid, and influenza were evaluated in PBMC derived from healthy adults and children. In addition, the potential anergic state of RV-specific T cells was analyzed by stimulation of PBMC with RV antigen in the presence of three anergy inhibitors (rIL-2, rIL-12, or DGKα-i). The quality and magnitude of RV-T cell responses were significantly lower than those of tetanus toxoid and influenza antigens. RV-CD4 T cell response was enriched in monofunctional IFN-γ+ cells, while influenza-CD4 and tetanus toxoid-CD4 T cell responses were enriched in multifunctional T cells. Moreover, rIL-2 - unlike rIL-12 or DGKα-i - increased the frequencies of RV-CD4 TNF-α+, CD4 IFN-γ+, and CD8 IFN-γ+ cells. Thus, circulating RV-T cells seem to have a relatively poor functional profile that may be partially reversed in vitro by the addition of rIL-2.

Original languageEnglish
Pages (from-to)340-350
Number of pages11
JournalVirology
Volume468
DOIs
StatePublished - 01 Nov 2014

Keywords

  • Cytokines
  • Proliferation
  • Rotavirus (RV)
  • T cells

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