Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis

Abstract Background Endometriosis is a known cause of infertility. Differences in immune tolerance caused by regulatory T cells (Tregs) and transforming growth factor-β (TGF-β) are thought to be involved in the pathology of endometriosis. Evidence has indicated that Tregs can be separated into three...

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Main Authors: Tetsuro Hanada, Shunichiro Tsuji, Misako Nakayama, Shiro Wakinoue, Kyoko Kasahara, Fuminori Kimura, Takahide Mori, Kazumasa Ogasawara, Takashi Murakami
Format: Article
Language:English
Published: BMC 2018-02-01
Series:Reproductive Biology and Endocrinology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12958-018-0325-2
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spelling doaj-2dd258593ec542b9a324d82b4c0f85fd2020-11-25T00:09:19ZengBMCReproductive Biology and Endocrinology1477-78272018-02-011611810.1186/s12958-018-0325-2Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosisTetsuro Hanada0Shunichiro Tsuji1Misako Nakayama2Shiro Wakinoue3Kyoko Kasahara4Fuminori Kimura5Takahide Mori6Kazumasa Ogasawara7Takashi Murakami8Department of Obstetrics and Gynecology, Shiga University of Medical ScienceDepartment of Obstetrics and Gynecology, Shiga University of Medical ScienceDepartment of Pathology, Division of Pathology and Disease Regulation, Shiga University of Medical ScienceDepartment of Obstetrics and Gynecology, Shiga University of Medical ScienceDepartment of Obstetrics and Gynecology, Shiga University of Medical ScienceDepartment of Obstetrics and Gynecology, Shiga University of Medical ScienceAcademia for Repro-Regenerative Medicine, Nonprofit OrganizationDepartment of Pathology, Division of Pathology and Disease Regulation, Shiga University of Medical ScienceDepartment of Obstetrics and Gynecology, Shiga University of Medical ScienceAbstract Background Endometriosis is a known cause of infertility. Differences in immune tolerance caused by regulatory T cells (Tregs) and transforming growth factor-β (TGF-β) are thought to be involved in the pathology of endometriosis. Evidence has indicated that Tregs can be separated into three functionally and phenotypically distinct subpopulations and that activated TGF-β is released from latency-associated peptide (LAP) on the surfaces of specific cells. The aim of this study was to examine differences in Treg subpopulations and LAP in the peripheral blood (PB) and peritoneal fluid (PF) of patients with and without endometriosis. Methods PB and PF were collected from 28 women with laparoscopically and histopathologically diagnosed endometriosis and 20 disease-free women who were subjected to laparoscopic surgery. Three subpopulations of CD4+ T lymphocytes (CD45RA+FoxP3low resting Tregs, CD45RA−FoxP3high effector Tregs, and CD45RA−FoxP3low non-Tregs) and CD11b+ mononuclear cells expressing LAP were analyzed by flow cytometry using specific monoclonal antibodies. Results Proportions of suppressive Tregs (resting and effector Tregs) were significantly higher in the PF samples of patients with endometriosis than in those of control women (P = 0.02 and P < 0.01, respectively) but did not differ between the PB samples of patients and controls. The percentage of CD11b+LAP+ macrophages was significantly lower in PF samples of patients with endometriosis than in those of controls (P < 0.01) but was not altered in the PB samples. Conclusion Proportions of suppressive Tregs and LAP+ macrophages are altered locally in the PF of endometriosis patients.http://link.springer.com/article/10.1186/s12958-018-0325-2Regulatory T cellTGF-βLatency-associated peptideEndometriosis
collection DOAJ
language English
format Article
sources DOAJ
author Tetsuro Hanada
Shunichiro Tsuji
Misako Nakayama
Shiro Wakinoue
Kyoko Kasahara
Fuminori Kimura
Takahide Mori
Kazumasa Ogasawara
Takashi Murakami
spellingShingle Tetsuro Hanada
Shunichiro Tsuji
Misako Nakayama
Shiro Wakinoue
Kyoko Kasahara
Fuminori Kimura
Takahide Mori
Kazumasa Ogasawara
Takashi Murakami
Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis
Reproductive Biology and Endocrinology
Regulatory T cell
TGF-β
Latency-associated peptide
Endometriosis
author_facet Tetsuro Hanada
Shunichiro Tsuji
Misako Nakayama
Shiro Wakinoue
Kyoko Kasahara
Fuminori Kimura
Takahide Mori
Kazumasa Ogasawara
Takashi Murakami
author_sort Tetsuro Hanada
title Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis
title_short Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis
title_full Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis
title_fullStr Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis
title_full_unstemmed Suppressive regulatory T cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis
title_sort suppressive regulatory t cells and latent transforming growth factor-β-expressing macrophages are altered in the peritoneal fluid of patients with endometriosis
publisher BMC
series Reproductive Biology and Endocrinology
issn 1477-7827
publishDate 2018-02-01
description Abstract Background Endometriosis is a known cause of infertility. Differences in immune tolerance caused by regulatory T cells (Tregs) and transforming growth factor-β (TGF-β) are thought to be involved in the pathology of endometriosis. Evidence has indicated that Tregs can be separated into three functionally and phenotypically distinct subpopulations and that activated TGF-β is released from latency-associated peptide (LAP) on the surfaces of specific cells. The aim of this study was to examine differences in Treg subpopulations and LAP in the peripheral blood (PB) and peritoneal fluid (PF) of patients with and without endometriosis. Methods PB and PF were collected from 28 women with laparoscopically and histopathologically diagnosed endometriosis and 20 disease-free women who were subjected to laparoscopic surgery. Three subpopulations of CD4+ T lymphocytes (CD45RA+FoxP3low resting Tregs, CD45RA−FoxP3high effector Tregs, and CD45RA−FoxP3low non-Tregs) and CD11b+ mononuclear cells expressing LAP were analyzed by flow cytometry using specific monoclonal antibodies. Results Proportions of suppressive Tregs (resting and effector Tregs) were significantly higher in the PF samples of patients with endometriosis than in those of control women (P = 0.02 and P < 0.01, respectively) but did not differ between the PB samples of patients and controls. The percentage of CD11b+LAP+ macrophages was significantly lower in PF samples of patients with endometriosis than in those of controls (P < 0.01) but was not altered in the PB samples. Conclusion Proportions of suppressive Tregs and LAP+ macrophages are altered locally in the PF of endometriosis patients.
topic Regulatory T cell
TGF-β
Latency-associated peptide
Endometriosis
url http://link.springer.com/article/10.1186/s12958-018-0325-2
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