Evaluation of the contribution of major T cell subsets to IFN-gamma production in TB infection by ELISPOT

Immunol Invest. 2009;38(5):341-9. doi: 10.1080/08820130902748744.

Abstract

Interferon gamma remains a key effector molecule that is still widely used as the most informative biomarker for screening human immune responses against tuberculosis, particularly in ELISPOT assays. We investigated the participation of CD4(+) and CD8(+) T lymphocytes in the PBMC responses to Mycobacterium tuberculosis (Mtb) specific antigens in 33 TB cases and 49 contacts. Responses to ESAT-6 were higher than CFP-10. There was no significant difference in responses to both Mtb antigens between cases and contacts. PBMCs response to ESAT-6 but not CFP-10 in cases was significantly reduced by depletion of CD4(+) cells whereas CD8(+) cell depletion had no impact. In conclusion, ESAT-6 is a more recognized antigen in this population, and CD4(+) lymphocytes are the main participants in IFN-gamma response by ELISPOT. Thus, a decline of CD4(+) T lymphocytes below a critical level might affect the sensitivity of IFN-gamma release assays for detecting Mtb infection.

MeSH terms

  • Adolescent
  • Adult
  • Antigens, Bacterial / immunology*
  • Bacterial Proteins / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Enzyme-Linked Immunosorbent Assay*
  • Female
  • Humans
  • Interferon-gamma / biosynthesis*
  • Male
  • Middle Aged
  • Tuberculosis / diagnosis
  • Tuberculosis / immunology*
  • Young Adult

Substances

  • Antigens, Bacterial
  • Bacterial Proteins
  • CFP-10 protein, Mycobacterium tuberculosis
  • ESAT-6 protein, Mycobacterium tuberculosis
  • Mycobacterium tuberculosis antigens
  • Interferon-gamma