4.2 Article

T cell responses to DosR and Rpf proteins in actively and latently infected individuals from Colombia

Journal

TUBERCULOSIS
Volume 92, Issue 2, Pages 148-159

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.tube.2011.12.005

Keywords

M. tuberculosis; DosR; Rpf; T-cell memory; Latency

Funding

  1. Colciencias
  2. Bogota
  3. Colombia
  4. Programa Estrategia de Sostenibilidad, Universidad de Antioquia, Medellin, Colombia
  5. [1115-459-21461]

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Mycobacterium tuberculosis DosR regulon-encoded proteins elicit strong immune T-cell responses in individuals with latent tuberculosis (LTBI). Also, resuscitation (Rpf) proteins can induce such responses. However, variations in the immunogenicity of the DosR and Rpf proteins have been observed in European and African populations, and no data are published from other geographic areas. In Colombian LTBI and patients with recently diagnosed PTB, we therefore studied the immune response to DosR, Rpf, stress, and nominal antigens fromMtb, in 7-day stimulated cultures. Three DosR (Rv1737c, Rv2029c, Rv2628c) and 2 Rpf (Rv0867 and Rv2389c) antigens were recognized most prominently on the basis of the net IFNg production (DosR) or the percentage of responding individuals (Rpf). Results show that the selected DosR antigens induced a higher proportion of CD4-T cells producing IFNg from LTBI, compared to pulmonary TB patients (PTB), while there were no differences in the proportion of CD8-T cells. An increased frequency of CD4, but not CD8 T-cells with a CD45RO(+)CD27(+) phenotype was observed in LTBI in response to Rv2029c, Rv0867c, and Rv2389c, compared to PTB. The levels of cytokines and chemokines in the supernatants of stimulated cells, showed that the DosR and Rpf antigens induced higher levels of IFN gamma in cultures from LTBI compared to PTB, although the induced pattern of cytokines and chemokines was also antigen dependent. In summary, our results are consistent with the significant immunogenicity of Mtb DosR and Rpf antigens in LTBI individuals, and confirm and extend previously reported data from other TB affected human populations. (C) 2011 Published by Elsevier Ltd.

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