Dysregulation of macrophage activation by decidual regulatory T cells in unexplained recurrent miscarriage patients
CD4 +CD25 + T cells (Treg cells) and macrophages play roles in the maintenance of maternal–fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell–cell contact and production of soluble factors. The purpose of this study was to investigate regul...
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Published in | Journal of reproductive immunology Vol. 92; no. 1; pp. 97 - 102 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Elsevier Ireland Ltd
01.12.2011
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ISSN | 0165-0378 1872-7603 1872-7603 |
DOI | 10.1016/j.jri.2011.08.004 |
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Abstract | CD4
+CD25
+ T cells (Treg cells) and macrophages play roles in the maintenance of maternal–fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell–cell contact and production of soluble factors. The purpose of this study was to investigate regulation of macrophages by Treg cells within decidua from patients with unexplained recurrent miscarriage (RM) and normal control women during early pregnancy. Treg cells and macrophages were isolated from deciduas of unexplained RM (
n
=
15) and control women (
n
=
15) by magnetic cell separation and co-cultured for six days. Regulation of macrophages by Treg cells was assessed in the presence and absence of neutralizing anti-TGFβ antibodies and in transwell experiments. Expression of CD80, CD86, IL10, and IFNγ by macrophages was measured by flow cytometry or ELISA. Macrophage expression of CD80 and CD86 was higher in deciduas of unexplained RM patients compared with controls whereas the expression of IL10 was lower. There was no difference in the expression of IFNγ by macrophages between the two groups. Treg cells inhibited macrophage expression of CD80, CD86 and IFNγ and increased the expression of IL10. The regulatory effects of Treg cells were abrogated in the presence of neutralizing anti-TGFβ antibodies or by transwell culture. The phenotype of macrophages therefore differed in unexplained RM patients compared with normal early pregnant subjects. Macrophage regulation by Treg cells was shown to be mediated by cell–cell contact and TGFβ and this capacity was decreased in unexplained RM patients. |
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AbstractList | CD4(+)CD25(+) T cells (Treg cells) and macrophages play roles in the maintenance of maternal-fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell-cell contact and production of soluble factors. The purpose of this study was to investigate regulation of macrophages by Treg cells within decidua from patients with unexplained recurrent miscarriage (RM) and normal control women during early pregnancy. Treg cells and macrophages were isolated from deciduas of unexplained RM (n=15) and control women (n=15) by magnetic cell separation and co-cultured for six days. Regulation of macrophages by Treg cells was assessed in the presence and absence of neutralizing anti-TGFβ antibodies and in transwell experiments. Expression of CD80, CD86, IL10, and IFNγ by macrophages was measured by flow cytometry or ELISA. Macrophage expression of CD80 and CD86 was higher in deciduas of unexplained RM patients compared with controls whereas the expression of IL10 was lower. There was no difference in the expression of IFNγ by macrophages between the two groups. Treg cells inhibited macrophage expression of CD80, CD86 and IFNγ and increased the expression of IL10. The regulatory effects of Treg cells were abrogated in the presence of neutralizing anti-TGFβ antibodies or by transwell culture. The phenotype of macrophages therefore differed in unexplained RM patients compared with normal early pregnant subjects. Macrophage regulation by Treg cells was shown to be mediated by cell-cell contact and TGFβ and this capacity was decreased in unexplained RM patients.CD4(+)CD25(+) T cells (Treg cells) and macrophages play roles in the maintenance of maternal-fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell-cell contact and production of soluble factors. The purpose of this study was to investigate regulation of macrophages by Treg cells within decidua from patients with unexplained recurrent miscarriage (RM) and normal control women during early pregnancy. Treg cells and macrophages were isolated from deciduas of unexplained RM (n=15) and control women (n=15) by magnetic cell separation and co-cultured for six days. Regulation of macrophages by Treg cells was assessed in the presence and absence of neutralizing anti-TGFβ antibodies and in transwell experiments. Expression of CD80, CD86, IL10, and IFNγ by macrophages was measured by flow cytometry or ELISA. Macrophage expression of CD80 and CD86 was higher in deciduas of unexplained RM patients compared with controls whereas the expression of IL10 was lower. There was no difference in the expression of IFNγ by macrophages between the two groups. Treg cells inhibited macrophage expression of CD80, CD86 and IFNγ and increased the expression of IL10. The regulatory effects of Treg cells were abrogated in the presence of neutralizing anti-TGFβ antibodies or by transwell culture. The phenotype of macrophages therefore differed in unexplained RM patients compared with normal early pregnant subjects. Macrophage regulation by Treg cells was shown to be mediated by cell-cell contact and TGFβ and this capacity was decreased in unexplained RM patients. CD4 +CD25 + T cells (Treg cells) and macrophages play roles in the maintenance of maternal–fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell–cell contact and production of soluble factors. The purpose of this study was to investigate regulation of macrophages by Treg cells within decidua from patients with unexplained recurrent miscarriage (RM) and normal control women during early pregnancy. Treg cells and macrophages were isolated from deciduas of unexplained RM ( n = 15) and control women ( n = 15) by magnetic cell separation and co-cultured for six days. Regulation of macrophages by Treg cells was assessed in the presence and absence of neutralizing anti-TGFβ antibodies and in transwell experiments. Expression of CD80, CD86, IL10, and IFNγ by macrophages was measured by flow cytometry or ELISA. Macrophage expression of CD80 and CD86 was higher in deciduas of unexplained RM patients compared with controls whereas the expression of IL10 was lower. There was no difference in the expression of IFNγ by macrophages between the two groups. Treg cells inhibited macrophage expression of CD80, CD86 and IFNγ and increased the expression of IL10. The regulatory effects of Treg cells were abrogated in the presence of neutralizing anti-TGFβ antibodies or by transwell culture. The phenotype of macrophages therefore differed in unexplained RM patients compared with normal early pregnant subjects. Macrophage regulation by Treg cells was shown to be mediated by cell–cell contact and TGFβ and this capacity was decreased in unexplained RM patients. CD4+CD25+ T cells (Treg cells) and macrophages play roles in the maintenance of maternal-fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell-cell contact and production of soluble factors. The purpose of this study was to investigate regulation of macrophages by Treg cells within decidua from patients with unexplained recurrent miscarriage (RM) and normal control women during early pregnancy. Treg cells and macrophages were isolated from deciduas of unexplained RM (n=15) and control women (n=15) by magnetic cell separation and co-cultured for six days. Regulation of macrophages by Treg cells was assessed in the presence and absence of neutralizing anti-TGF beta antibodies and in transwell experiments. Expression of CD80, CD86, IL10, and IFN gamma by macrophages was measured by flow cytometry or ELISA. Macrophage expression of CD80 and CD86 was higher in deciduas of unexplained RM patients compared with controls whereas the expression of IL10 was lower. There was no difference in the expression of IFN gamma by macrophages between the two groups. Treg cells inhibited macrophage expression of CD80, CD86 and IFN gamma and increased the expression of IL10. The regulatory effects of Treg cells were abrogated in the presence of neutralizing anti-TGF beta antibodies or by transwell culture. The phenotype of macrophages therefore differed in unexplained RM patients compared with normal early pregnant subjects. Macrophage regulation by Treg cells was shown to be mediated by cell-cell contact and TGF beta and this capacity was decreased in unexplained RM patients. CD4(+)CD25(+) T cells (Treg cells) and macrophages play roles in the maintenance of maternal-fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell-cell contact and production of soluble factors. The purpose of this study was to investigate regulation of macrophages by Treg cells within decidua from patients with unexplained recurrent miscarriage (RM) and normal control women during early pregnancy. Treg cells and macrophages were isolated from deciduas of unexplained RM (n=15) and control women (n=15) by magnetic cell separation and co-cultured for six days. Regulation of macrophages by Treg cells was assessed in the presence and absence of neutralizing anti-TGFβ antibodies and in transwell experiments. Expression of CD80, CD86, IL10, and IFNγ by macrophages was measured by flow cytometry or ELISA. Macrophage expression of CD80 and CD86 was higher in deciduas of unexplained RM patients compared with controls whereas the expression of IL10 was lower. There was no difference in the expression of IFNγ by macrophages between the two groups. Treg cells inhibited macrophage expression of CD80, CD86 and IFNγ and increased the expression of IL10. The regulatory effects of Treg cells were abrogated in the presence of neutralizing anti-TGFβ antibodies or by transwell culture. The phenotype of macrophages therefore differed in unexplained RM patients compared with normal early pregnant subjects. Macrophage regulation by Treg cells was shown to be mediated by cell-cell contact and TGFβ and this capacity was decreased in unexplained RM patients. Abstract CD4+ CD25+ T cells (Treg cells) and macrophages play roles in the maintenance of maternal–fetal immunological tolerance. Treg cells suppress the function of macrophages via mechanisms mediated by cell–cell contact and production of soluble factors. The purpose of this study was to investigate regulation of macrophages by Treg cells within decidua from patients with unexplained recurrent miscarriage (RM) and normal control women during early pregnancy. Treg cells and macrophages were isolated from deciduas of unexplained RM ( n = 15) and control women ( n = 15) by magnetic cell separation and co-cultured for six days. Regulation of macrophages by Treg cells was assessed in the presence and absence of neutralizing anti-TGFβ antibodies and in transwell experiments. Expression of CD80, CD86, IL10, and IFNγ by macrophages was measured by flow cytometry or ELISA. Macrophage expression of CD80 and CD86 was higher in deciduas of unexplained RM patients compared with controls whereas the expression of IL10 was lower. There was no difference in the expression of IFNγ by macrophages between the two groups. Treg cells inhibited macrophage expression of CD80, CD86 and IFNγ and increased the expression of IL10. The regulatory effects of Treg cells were abrogated in the presence of neutralizing anti-TGFβ antibodies or by transwell culture. The phenotype of macrophages therefore differed in unexplained RM patients compared with normal early pregnant subjects. Macrophage regulation by Treg cells was shown to be mediated by cell–cell contact and TGFβ and this capacity was decreased in unexplained RM patients. |
Author | Hao, Cui-Fang Wang, Wen-Juan Lin, Qi-De |
Author_xml | – sequence: 1 givenname: Wen-Juan surname: Wang fullname: Wang, Wen-Juan email: sdwangwj@126.com organization: Reproduction Medical Center, Yantai Yuhuangding Hospital, Qingdao University School of Medicine, 20 Yuhuangding East Road, Yantai 264000, China – sequence: 2 givenname: Cui-Fang surname: Hao fullname: Hao, Cui-Fang organization: Reproduction Medical Center, Yantai Yuhuangding Hospital, Qingdao University School of Medicine, 20 Yuhuangding East Road, Yantai 264000, China – sequence: 3 givenname: Qi-De surname: Lin fullname: Lin, Qi-De email: linqide2007@126.com organization: Department of Obstetrics and Gynecology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, 145 Shandong Mid Road, Shanghai 200001, China |
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Keywords | Costimulatory molecules Interleukin-10 Miscarriage Regulatory T cells Interferon-γ Macrophage Human Relapse Pregnancy disorders Cytokine Activation Abortion Vertebrata Mammalia Interleukin 10 T-Lymphocyte Gamma interferon |
Language | English |
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Snippet | CD4
+CD25
+ T cells (Treg cells) and macrophages play roles in the maintenance of maternal–fetal immunological tolerance. Treg cells suppress the function of... Abstract CD4+ CD25+ T cells (Treg cells) and macrophages play roles in the maintenance of maternal–fetal immunological tolerance. Treg cells suppress the... CD4(+)CD25(+) T cells (Treg cells) and macrophages play roles in the maintenance of maternal-fetal immunological tolerance. Treg cells suppress the function of... CD4+CD25+ T cells (Treg cells) and macrophages play roles in the maintenance of maternal-fetal immunological tolerance. Treg cells suppress the function of... |
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SubjectTerms | Abortion, Habitual - immunology Adult Antibodies, Blocking - pharmacology Antigens, CD - metabolism Biological and medical sciences Cell Communication - drug effects Cell Communication - immunology Cells, Cultured Coculture Techniques Costimulatory molecules Decidua - pathology Embryology: invertebrates and vertebrates. Teratology Female Fundamental and applied biological sciences. Psychology Gene Expression Regulation - drug effects Humans Interferon-gamma - genetics Interferon-gamma - metabolism Interferon-γ Interleukin-10 Interleukin-10 - genetics Interleukin-10 - immunology Interleukin-10 - metabolism Macrophage Macrophage Activation - drug effects Macrophages - drug effects Macrophages - immunology Macrophages - metabolism Macrophages - pathology Miscarriage Obstetrics and Gynecology Regulatory T cells T-Lymphocytes, Regulatory - drug effects T-Lymphocytes, Regulatory - immunology T-Lymphocytes, Regulatory - metabolism T-Lymphocytes, Regulatory - pathology Transforming Growth Factor beta - immunology Transforming Growth Factor beta - metabolism |
Title | Dysregulation of macrophage activation by decidual regulatory T cells in unexplained recurrent miscarriage patients |
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