The frequencies of IFNγ+IL2+TNFα+ PPD-specific CD4+CD45RO+ T-cells correlate with the magnitude of the QuantiFERON® gold in-tube response in a prospective study of healthy indian adolescents

PLoS One. 2014 Jul 3;9(7):e101224. doi: 10.1371/journal.pone.0101224. eCollection 2014.

Abstract

Background: QuantiFERON-TB Gold In-Tube (QFT) is an IFNγ-release assay used in the diagnosis of Mycobacterium tuberculosis (MTB) infection. The risk of TB progression increases with the magnitude of the MTB-specific IFNγ-response. QFT reversion, also associated with low Tuberculin Skin Test responses, may therefore represent a transient immune response with control of M. tuberculosis infection. However, studies at the single cell level have suggested that the quality (polyfunctionality) of the T-cell response is more important than the quantity of cytokines produced.

Objective: To explore the quality and/or magnitude of mycobacteria-specific T-cell responses associated with QFT reversion and persistent QFT-positivity.

Methods: Multi-color flowcytometry on prospectively collected peripheral blood mononuclear cells was applied to assess mycobacteria-specific T-cell responses in 42 QFT positive Indian adolescents of whom 21 became QFT negative (reverters) within one year. Ten QFT consistent negatives were also included as controls.

Results: There was no difference in the qualitative PPD-specific CD4+ T-cell response between QFT consistent positives and reverters. However, compared with QFT consistent positives, reverters displayed lower absolute frequencies of polyfunctional (IFNγ+IL2+TNFα+) CD4+ T-cells at baseline, which were further reduced to the point where they were not different to QFT negative controls one year later. Moreover, absolute frequencies of these cells correlated well with the magnitude of the QFT-response.

Conclusion: Whereas specific polyfunctional CD4+ T-cells have been suggested to protect against TB progression, our data do not support that higher relative or absolute frequencies of PPD-specific polyfunctional CD4+ T-cells in peripheral blood can explain the reduced risk of TB progression observed in QFT reverters. On the contrary, absolute frequencies of these cells correlated with the QFT-response, suggesting that this readout reflects antigenic load.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Asian People
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • Child
  • Cohort Studies
  • Gold / chemistry
  • Humans
  • India
  • Interferon-gamma / metabolism*
  • Interleukin-2 / metabolism*
  • Leukocyte Common Antigens / metabolism*
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Prospective Studies
  • Reagent Kits, Diagnostic
  • Tuberculosis / diagnosis
  • Tuberculosis / immunology
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Interleukin-2
  • Reagent Kits, Diagnostic
  • Tumor Necrosis Factor-alpha
  • Gold
  • Interferon-gamma
  • Leukocyte Common Antigens

Grants and funding

This study was supported by the Research Council of Norway (http://www.forskningsradet.no/en/), grants 179342 and 192534, the University of Bergen, Norway (http://www.uib.no/en), Aeras, USA (http://www.aeras.org/) and St. John’s Research Institute, India (http://www.sjri.res.in/). Synne Jenum received a doctoral stipend covered by grant 179342 (Research council of Norway), administered and coordinated by University of Bergen, Norway. The work was also partly supported by the Research Council of Norway through its Centres of Excellence funding scheme, project number 179573. QFT kits were supported in part by Foundation for Innovative New Diagnostics (http://www.finddiagnostics.org/). Larry Geiter, formerly at Aeras contributed to the initial protocol development of the Adolescent Cohort Study. Ravi Anantha and Lew Barker, also at Aeras, reviewed the manuscript prior to submission. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.