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

( ) 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 antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial...

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Published inFrontiers in immunology Vol. 10; p. 2807
Main Authors Yamashita, Yoshiro, Oe, Toshiyuki, Kawakami, Kenji, Osada-Oka, Mayuko, Ozeki, Yuriko, Terahara, Kazutaka, Yasuda, Ikkoh, Edwards, Tansy, Tanaka, Takeshi, Tsunetsugu-Yokota, Yasuko, Matsumoto, Sohkichi, Ariyoshi, Koya
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 29.11.2019
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Summary:( ) 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 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 infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of -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 antigens, specifically IL-10 response against Acr in latent 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.
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Reviewed by: Sadhna Sharma, Miranda House - University College for Women, India; Roberta Olmo Pinheiro, Oswaldo Cruz Foundation (Fiocruz), Brazil
This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology
Edited by: Mario Alberto Flores-Valdez, CONACYT Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ), Mexico
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2019.02807