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Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients

Although the pathogenesis of sarcoidosis is not fully understood, immunological characterization has elucidated highly polarized expression of the type 1 T helper cell response. Mucosal-associated invariant T (MAIT) cells are innate T cells that recognize bacterial riboflavin and rapidly produce cyt...

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Autores principales: Matsuyama, Hisayo, Isshiki, Takuma, Chiba, Asako, Yamaguchi, Tetsuo, Murayama, Goh, Akasaka, Yoshikiyo, Eishi, Yoshinobu, Sakamoto, Susumu, Homma, Sakae, Miyake, Sachiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742655/
https://www.ncbi.nlm.nih.gov/pubmed/31515495
http://dx.doi.org/10.1038/s41598-019-49903-6
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author Matsuyama, Hisayo
Isshiki, Takuma
Chiba, Asako
Yamaguchi, Tetsuo
Murayama, Goh
Akasaka, Yoshikiyo
Eishi, Yoshinobu
Sakamoto, Susumu
Homma, Sakae
Miyake, Sachiko
author_facet Matsuyama, Hisayo
Isshiki, Takuma
Chiba, Asako
Yamaguchi, Tetsuo
Murayama, Goh
Akasaka, Yoshikiyo
Eishi, Yoshinobu
Sakamoto, Susumu
Homma, Sakae
Miyake, Sachiko
author_sort Matsuyama, Hisayo
collection PubMed
description Although the pathogenesis of sarcoidosis is not fully understood, immunological characterization has elucidated highly polarized expression of the type 1 T helper cell response. Mucosal-associated invariant T (MAIT) cells are innate T cells that recognize bacterial riboflavin and rapidly produce cytokines such as interferon γ and tumor necrosis factor α. We prospectively evaluated the proportion of MAIT cells and the expression levels of cell surface markers in peripheral blood from 40 sarcoidosis patients and 28 healthy controls. MAIT cells in bronchoalveolar lavage fluid (BALF) were also examined in 12 sarcoidosis patients. In peripheral blood, the proportion of MAIT cells was lower (P = 0.0002), but the expression levels of CD69 and programmed death 1 on MAIT cells were higher in sarcoidosis patients than in healthy controls. Moreover, CD69 expression levels were significantly correlated with clinical biomarkers. Sarcoidosis patients with parenchymal infiltration in the lungs showed a significantly higher proportion and number of MAIT cells in BALF compared to patients without parenchymal infiltration. CD69 expression levels on MAIT cells in BALF were higher than levels in peripheral blood. The activation status of MAIT cells might reflect the disease activity of sarcoidosis. Therefore, it is a potential target for sarcoidosis treatment.
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spelling pubmed-67426552019-09-26 Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients Matsuyama, Hisayo Isshiki, Takuma Chiba, Asako Yamaguchi, Tetsuo Murayama, Goh Akasaka, Yoshikiyo Eishi, Yoshinobu Sakamoto, Susumu Homma, Sakae Miyake, Sachiko Sci Rep Article Although the pathogenesis of sarcoidosis is not fully understood, immunological characterization has elucidated highly polarized expression of the type 1 T helper cell response. Mucosal-associated invariant T (MAIT) cells are innate T cells that recognize bacterial riboflavin and rapidly produce cytokines such as interferon γ and tumor necrosis factor α. We prospectively evaluated the proportion of MAIT cells and the expression levels of cell surface markers in peripheral blood from 40 sarcoidosis patients and 28 healthy controls. MAIT cells in bronchoalveolar lavage fluid (BALF) were also examined in 12 sarcoidosis patients. In peripheral blood, the proportion of MAIT cells was lower (P = 0.0002), but the expression levels of CD69 and programmed death 1 on MAIT cells were higher in sarcoidosis patients than in healthy controls. Moreover, CD69 expression levels were significantly correlated with clinical biomarkers. Sarcoidosis patients with parenchymal infiltration in the lungs showed a significantly higher proportion and number of MAIT cells in BALF compared to patients without parenchymal infiltration. CD69 expression levels on MAIT cells in BALF were higher than levels in peripheral blood. The activation status of MAIT cells might reflect the disease activity of sarcoidosis. Therefore, it is a potential target for sarcoidosis treatment. Nature Publishing Group UK 2019-09-12 /pmc/articles/PMC6742655/ /pubmed/31515495 http://dx.doi.org/10.1038/s41598-019-49903-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Matsuyama, Hisayo
Isshiki, Takuma
Chiba, Asako
Yamaguchi, Tetsuo
Murayama, Goh
Akasaka, Yoshikiyo
Eishi, Yoshinobu
Sakamoto, Susumu
Homma, Sakae
Miyake, Sachiko
Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients
title Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients
title_full Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients
title_fullStr Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients
title_full_unstemmed Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients
title_short Activation of mucosal-associated invariant T cells in the lungs of sarcoidosis patients
title_sort activation of mucosal-associated invariant t cells in the lungs of sarcoidosis patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742655/
https://www.ncbi.nlm.nih.gov/pubmed/31515495
http://dx.doi.org/10.1038/s41598-019-49903-6
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