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Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome

BACKGROUND: Immune dysfunction is one of the mechanisms to promote polycystic ovary syndrome (PCOS). Various immune cells have been reported to be involved in the development of PCOS. Meanwhile, the disturbance of metabolism is closely related to PCOS. The aim of this study is to explore the associa...

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Autores principales: Zhu, Mengting, Xu, Yuping, Li, Caihua, Lu, Zhimin, Bi, Kaihuan, Wang, Kangxia, Guo, Peipei, Jiang, Huanhuan, Cao, Yunxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630849/
https://www.ncbi.nlm.nih.gov/pubmed/34847942
http://dx.doi.org/10.1186/s12958-021-00861-7
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author Zhu, Mengting
Xu, Yuping
Li, Caihua
Lu, Zhimin
Bi, Kaihuan
Wang, Kangxia
Guo, Peipei
Jiang, Huanhuan
Cao, Yunxia
author_facet Zhu, Mengting
Xu, Yuping
Li, Caihua
Lu, Zhimin
Bi, Kaihuan
Wang, Kangxia
Guo, Peipei
Jiang, Huanhuan
Cao, Yunxia
author_sort Zhu, Mengting
collection PubMed
description BACKGROUND: Immune dysfunction is one of the mechanisms to promote polycystic ovary syndrome (PCOS). Various immune cells have been reported to be involved in the development of PCOS. Meanwhile, the disturbance of metabolism is closely related to PCOS. The aim of this study is to explore the association of mucosal-associated invariant T (MAIT) cells and myeloid-derived suppressor cells (MDSCs) with the metabolic dysfunction in PCOS. METHODS: 68 PCOS patients and 40 controls were recruited in this study and we collected the peripheral blood of participants’ during their follicular phase. The frequencies of MAIT cells and MDSCs were determined by flow cytometry after being stained with different monoclonal antibodies. And the concentrations of cytokines were determined by ELISA. RESULTS: Compared to controls with normal metabolism, the frequency of MDSCs, CD8(+)MAIT cells and CD38(+)CD8(+)MAIT cells were significantly decreased in PCOS patients with normal metabolism, however, proportion of CD4(+)MAIT cells exhibited a noticeable increase. Similar results of CD8(+)MAIT, CD38(+)CD8(+)MAIT cells and reduced expression of IL-17 were observed in PCOS patients with metabolic dysfunction as compared to controls with metabolic disorders. PCOS patients with excessive testosterone levels displayed significantly decreased levels of CD8(+)MAIT, CD38(+)CD8(+)MAIT cells, MDSCs and Mo-MDSCs as compared to PCOS patients with normal testosterone concentrations. PCOS patients with abnormal weight showed a lower level and activation of CD8(+)MAIT cells. On the contrary, they displayed an enrichment of CD4(+)MAIT cells. PCOS patients with glucose metabolic disorder displayed a remarkable dysregulation of MDSCs and Mo-MDSCs. MDSCs were positively correlated with MAIT cells. Negative correlations between the frequency of CD8(+)MAIT cells, CD38(+)CD8(+)MAIT cells and body mass index were revealed. CD4(+)MAIT cells positively correlated with BMI. Mo-MDSCs were found to be negatively related to the levels of 2hour plasma glucose and HOMA-IR index. CONCLUSION: The impairment of CD8+MAIT cells and MDSCs is involved in the metabolic dysfunction of PCOS.
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spelling pubmed-86308492021-12-01 Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome Zhu, Mengting Xu, Yuping Li, Caihua Lu, Zhimin Bi, Kaihuan Wang, Kangxia Guo, Peipei Jiang, Huanhuan Cao, Yunxia Reprod Biol Endocrinol Research BACKGROUND: Immune dysfunction is one of the mechanisms to promote polycystic ovary syndrome (PCOS). Various immune cells have been reported to be involved in the development of PCOS. Meanwhile, the disturbance of metabolism is closely related to PCOS. The aim of this study is to explore the association of mucosal-associated invariant T (MAIT) cells and myeloid-derived suppressor cells (MDSCs) with the metabolic dysfunction in PCOS. METHODS: 68 PCOS patients and 40 controls were recruited in this study and we collected the peripheral blood of participants’ during their follicular phase. The frequencies of MAIT cells and MDSCs were determined by flow cytometry after being stained with different monoclonal antibodies. And the concentrations of cytokines were determined by ELISA. RESULTS: Compared to controls with normal metabolism, the frequency of MDSCs, CD8(+)MAIT cells and CD38(+)CD8(+)MAIT cells were significantly decreased in PCOS patients with normal metabolism, however, proportion of CD4(+)MAIT cells exhibited a noticeable increase. Similar results of CD8(+)MAIT, CD38(+)CD8(+)MAIT cells and reduced expression of IL-17 were observed in PCOS patients with metabolic dysfunction as compared to controls with metabolic disorders. PCOS patients with excessive testosterone levels displayed significantly decreased levels of CD8(+)MAIT, CD38(+)CD8(+)MAIT cells, MDSCs and Mo-MDSCs as compared to PCOS patients with normal testosterone concentrations. PCOS patients with abnormal weight showed a lower level and activation of CD8(+)MAIT cells. On the contrary, they displayed an enrichment of CD4(+)MAIT cells. PCOS patients with glucose metabolic disorder displayed a remarkable dysregulation of MDSCs and Mo-MDSCs. MDSCs were positively correlated with MAIT cells. Negative correlations between the frequency of CD8(+)MAIT cells, CD38(+)CD8(+)MAIT cells and body mass index were revealed. CD4(+)MAIT cells positively correlated with BMI. Mo-MDSCs were found to be negatively related to the levels of 2hour plasma glucose and HOMA-IR index. CONCLUSION: The impairment of CD8+MAIT cells and MDSCs is involved in the metabolic dysfunction of PCOS. BioMed Central 2021-11-30 /pmc/articles/PMC8630849/ /pubmed/34847942 http://dx.doi.org/10.1186/s12958-021-00861-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhu, Mengting
Xu, Yuping
Li, Caihua
Lu, Zhimin
Bi, Kaihuan
Wang, Kangxia
Guo, Peipei
Jiang, Huanhuan
Cao, Yunxia
Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome
title Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome
title_full Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome
title_fullStr Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome
title_full_unstemmed Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome
title_short Involvement of impaired CD8(+) mucosal-associated invariant T cells and myeloid-derived suppressor cells in polycystic ovary syndrome
title_sort involvement of impaired cd8(+) mucosal-associated invariant t cells and myeloid-derived suppressor cells in polycystic ovary syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630849/
https://www.ncbi.nlm.nih.gov/pubmed/34847942
http://dx.doi.org/10.1186/s12958-021-00861-7
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