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CD4+ T Responses Other Than Th1 Type Are Preferentially Induced by Latency-Associated Antigens in the State of Latent Mycobacterium tuberculosis Infection

  • Yoshiro Yamashita
  • , Toshiyuki Oe
  • , Kenji Kawakami
  • , Mayuko Osada-Oka
  • , Yuriko Ozeki
  • , Kazutaka Terahara
  • , Ikkoh Yasuda
  • , Tansy Edwards
  • , Takeshi Tanaka
  • , Yasuko Tsunetsugu-Yokota
  • , Sohkichi Matsumoto
  • , Koya Ariyoshi
  • Nagasaki University
  • National Hospital Organization Higashi-Saga Hospital
  • National Hospital Organization Nagasaki Kawatana Medical Center
  • Kyoto Prefectural University
  • Niigata University
  • National Institute of Infectious Diseases
  • London School of Hygiene and Tropical Medicine
  • Tokyo University of Technology
  • Universitas Airlangga
  • School of Tropical Medicine and Global Health

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

Mycobacterium tuberculosis (M. tuberculosis) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4+ T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated M. tuberculosis antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial DNA-binding protein 1 (MDP-1) remain elusive in relation to the clinical stage of M. tuberculosis infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of M. tuberculosis-infected cases and control PBMCs were stimulated with these antigens and ESAT-6/CFP-10. Cytokine profiles of CD4+ T cells were evaluated by intracellular cytokine staining using multicolor flow cytometry. Our results demonstrate that Th1 cytokine responses were predominant after TB onset independent of the type of antigen stimulation. On the contrary, non-Th1 cytokine responses were preferentially induced by latency-associated M. tuberculosis antigens, specifically IL-10 response against Acr in latent M. tuberculosis infection. From these results, we surmise a shift in the CD4+ T cell response from mixed non-Th1 to Th1 dominant type during TB progression.

Original languageEnglish
Article number2807
JournalFrontiers in Immunology
Volume10
DOIs
Publication statusPublished - 29 Nov 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acr
  • CD4 T cells
  • HBHA
  • latent M. tuberculosis infection
  • MDP-1
  • non-Th1

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