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Myeloid‐derived suppressor cells in obstetrical and gynecological diseases
Myeloid‐derived suppressor cells (MDSCs) are a heterogeneous group of myeloid‐origin cells which have immunosuppressive activities in several conditions, such as cancer and inflammation. Recent research has also associated MDSCs with numerous obstetrical and gynecological diseases. During pregnancy,...
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Published in: | American journal of reproductive immunology (1989) 2020-08, Vol.84 (2), p.e13266-n/a |
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container_title | American journal of reproductive immunology (1989) |
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creator | Zheng, Zi‐Meng Yang, Hui‐Li Lai, Zhen‐Zhen Wang, Cheng‐Jie Yang, Shao‐Liang Li, Ming‐Qing Shao, Jun |
description | Myeloid‐derived suppressor cells (MDSCs) are a heterogeneous group of myeloid‐origin cells which have immunosuppressive activities in several conditions, such as cancer and inflammation. Recent research has also associated MDSCs with numerous obstetrical and gynecological diseases. During pregnancy, MDSCs accumulate to ensure maternal‐fetal immune tolerance, whereas they are decreased in patients who suffer from early miscarriage or pre‐eclampsia. While the etiology of endometriosis is still unknown, abnormal accumulation of MDSCs in the peripheral blood and peritoneal fluid, alongside an increased level of reactive oxygen species (ROS), has been observed in these patients, which is central to the cellular immune regulations by MDSCs. Additionally, the regulation of MDSCs observed in tumours is also applicable to gynecologic neoplasms, including ovarian cancer and cervical cancer. More recently, emerging evidence has shown that there are high levels of MDSCs in premature ovarian failure (POF) and in vitro fertilization (IVF), but the underlying mechanisms are unknown. In this review, the generation and mechanisms of MDSCs are summarized. In particular, the modulation of these cells in immune‐related obstetrical and gynecological diseases is discussed, including potential treatment options targeting MDSCs. |
doi_str_mv | 10.1111/aji.13266 |
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Recent research has also associated MDSCs with numerous obstetrical and gynecological diseases. During pregnancy, MDSCs accumulate to ensure maternal‐fetal immune tolerance, whereas they are decreased in patients who suffer from early miscarriage or pre‐eclampsia. While the etiology of endometriosis is still unknown, abnormal accumulation of MDSCs in the peripheral blood and peritoneal fluid, alongside an increased level of reactive oxygen species (ROS), has been observed in these patients, which is central to the cellular immune regulations by MDSCs. Additionally, the regulation of MDSCs observed in tumours is also applicable to gynecologic neoplasms, including ovarian cancer and cervical cancer. More recently, emerging evidence has shown that there are high levels of MDSCs in premature ovarian failure (POF) and in vitro fertilization (IVF), but the underlying mechanisms are unknown. In this review, the generation and mechanisms of MDSCs are summarized. In particular, the modulation of these cells in immune‐related obstetrical and gynecological diseases is discussed, including potential treatment options targeting MDSCs.</description><identifier>ISSN: 1046-7408</identifier><identifier>EISSN: 1600-0897</identifier><identifier>DOI: 10.1111/aji.13266</identifier><identifier>PMID: 32418253</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Cervical cancer ; Cervix ; Eclampsia ; Endometriosis ; Etiology ; Fetuses ; gynecologic neoplasms ; Gynecological diseases ; Gynecology ; Immunological tolerance ; In vitro fertilization ; miscarriage ; myeloid‐derived suppressor cells ; Ovarian cancer ; Peripheral blood ; Peritoneal fluid ; Peritoneum ; Preeclampsia ; Pregnancy ; pre‐eclampsia ; Reactive oxygen species ; Reproductive status ; Suppressor cells ; Therapeutic applications ; Tumors</subject><ispartof>American journal of reproductive immunology (1989), 2020-08, Vol.84 (2), p.e13266-n/a</ispartof><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-3f9229fcb9e70d52c6756dbdc590c1f3951eb294bfc5cb5a624348a9d0bc74bb3</citedby><cites>FETCH-LOGICAL-c3536-3f9229fcb9e70d52c6756dbdc590c1f3951eb294bfc5cb5a624348a9d0bc74bb3</cites><orcidid>0000-0002-9276-0722 ; 0000-0002-6493-4086</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32418253$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheng, Zi‐Meng</creatorcontrib><creatorcontrib>Yang, Hui‐Li</creatorcontrib><creatorcontrib>Lai, Zhen‐Zhen</creatorcontrib><creatorcontrib>Wang, Cheng‐Jie</creatorcontrib><creatorcontrib>Yang, Shao‐Liang</creatorcontrib><creatorcontrib>Li, Ming‐Qing</creatorcontrib><creatorcontrib>Shao, Jun</creatorcontrib><title>Myeloid‐derived suppressor cells in obstetrical and gynecological diseases</title><title>American journal of reproductive immunology (1989)</title><addtitle>Am J Reprod Immunol</addtitle><description>Myeloid‐derived suppressor cells (MDSCs) are a heterogeneous group of myeloid‐origin cells which have immunosuppressive activities in several conditions, such as cancer and inflammation. Recent research has also associated MDSCs with numerous obstetrical and gynecological diseases. During pregnancy, MDSCs accumulate to ensure maternal‐fetal immune tolerance, whereas they are decreased in patients who suffer from early miscarriage or pre‐eclampsia. While the etiology of endometriosis is still unknown, abnormal accumulation of MDSCs in the peripheral blood and peritoneal fluid, alongside an increased level of reactive oxygen species (ROS), has been observed in these patients, which is central to the cellular immune regulations by MDSCs. Additionally, the regulation of MDSCs observed in tumours is also applicable to gynecologic neoplasms, including ovarian cancer and cervical cancer. More recently, emerging evidence has shown that there are high levels of MDSCs in premature ovarian failure (POF) and in vitro fertilization (IVF), but the underlying mechanisms are unknown. In this review, the generation and mechanisms of MDSCs are summarized. In particular, the modulation of these cells in immune‐related obstetrical and gynecological diseases is discussed, including potential treatment options targeting MDSCs.</description><subject>Cervical cancer</subject><subject>Cervix</subject><subject>Eclampsia</subject><subject>Endometriosis</subject><subject>Etiology</subject><subject>Fetuses</subject><subject>gynecologic neoplasms</subject><subject>Gynecological diseases</subject><subject>Gynecology</subject><subject>Immunological tolerance</subject><subject>In vitro fertilization</subject><subject>miscarriage</subject><subject>myeloid‐derived suppressor cells</subject><subject>Ovarian cancer</subject><subject>Peripheral blood</subject><subject>Peritoneal fluid</subject><subject>Peritoneum</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>pre‐eclampsia</subject><subject>Reactive oxygen species</subject><subject>Reproductive status</subject><subject>Suppressor cells</subject><subject>Therapeutic applications</subject><subject>Tumors</subject><issn>1046-7408</issn><issn>1600-0897</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKA0EQRRtRTIwu_AEZcKOL0X7No5ch-IhE3Oh66EdN6DCZjt0ZZXZ-gt_ol9gm6kKwNlVcDrcuF6Fjgi9InEu5sBeE0TzfQUOSY5ziUhS78cY8TwuOywE6CGGBcdRZsY8GjHJS0owN0ey-h8ZZ8_H2bsDbFzBJ6FYrDyE4n2hompDYNnEqrGHtrZZNIluTzPsWtGvcfKMYG0AGCIdor5ZNgKPvPUJP11ePk9t09nAznYxnqWYZy1NWC0pFrZWAApuM6rzIcqOMzgTWpGYiI6Co4KrWmVaZzClnvJTCYKULrhQbobOt78q75w7Culra8JVVtuC6UFGOOSuJiN9G6PQPunCdb2O6SFFW0oJTEqnzLaW9C8FDXa28XUrfVwRXXxVXseJqU3FkT74dO7UE80v-dBqByy3wahvo_3eqxnfTreUnDeOGPw</recordid><startdate>202008</startdate><enddate>202008</enddate><creator>Zheng, Zi‐Meng</creator><creator>Yang, Hui‐Li</creator><creator>Lai, Zhen‐Zhen</creator><creator>Wang, Cheng‐Jie</creator><creator>Yang, Shao‐Liang</creator><creator>Li, Ming‐Qing</creator><creator>Shao, Jun</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9276-0722</orcidid><orcidid>https://orcid.org/0000-0002-6493-4086</orcidid></search><sort><creationdate>202008</creationdate><title>Myeloid‐derived suppressor cells in obstetrical and gynecological diseases</title><author>Zheng, Zi‐Meng ; Yang, Hui‐Li ; Lai, Zhen‐Zhen ; Wang, Cheng‐Jie ; Yang, Shao‐Liang ; Li, Ming‐Qing ; Shao, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-3f9229fcb9e70d52c6756dbdc590c1f3951eb294bfc5cb5a624348a9d0bc74bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cervical cancer</topic><topic>Cervix</topic><topic>Eclampsia</topic><topic>Endometriosis</topic><topic>Etiology</topic><topic>Fetuses</topic><topic>gynecologic neoplasms</topic><topic>Gynecological diseases</topic><topic>Gynecology</topic><topic>Immunological tolerance</topic><topic>In vitro fertilization</topic><topic>miscarriage</topic><topic>myeloid‐derived suppressor cells</topic><topic>Ovarian cancer</topic><topic>Peripheral blood</topic><topic>Peritoneal fluid</topic><topic>Peritoneum</topic><topic>Preeclampsia</topic><topic>Pregnancy</topic><topic>pre‐eclampsia</topic><topic>Reactive oxygen species</topic><topic>Reproductive status</topic><topic>Suppressor cells</topic><topic>Therapeutic applications</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Zi‐Meng</creatorcontrib><creatorcontrib>Yang, Hui‐Li</creatorcontrib><creatorcontrib>Lai, Zhen‐Zhen</creatorcontrib><creatorcontrib>Wang, Cheng‐Jie</creatorcontrib><creatorcontrib>Yang, Shao‐Liang</creatorcontrib><creatorcontrib>Li, Ming‐Qing</creatorcontrib><creatorcontrib>Shao, Jun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of reproductive immunology (1989)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Zi‐Meng</au><au>Yang, Hui‐Li</au><au>Lai, Zhen‐Zhen</au><au>Wang, Cheng‐Jie</au><au>Yang, Shao‐Liang</au><au>Li, Ming‐Qing</au><au>Shao, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Myeloid‐derived suppressor cells in obstetrical and gynecological diseases</atitle><jtitle>American journal of reproductive immunology (1989)</jtitle><addtitle>Am J Reprod Immunol</addtitle><date>2020-08</date><risdate>2020</risdate><volume>84</volume><issue>2</issue><spage>e13266</spage><epage>n/a</epage><pages>e13266-n/a</pages><issn>1046-7408</issn><eissn>1600-0897</eissn><abstract>Myeloid‐derived suppressor cells (MDSCs) are a heterogeneous group of myeloid‐origin cells which have immunosuppressive activities in several conditions, such as cancer and inflammation. Recent research has also associated MDSCs with numerous obstetrical and gynecological diseases. During pregnancy, MDSCs accumulate to ensure maternal‐fetal immune tolerance, whereas they are decreased in patients who suffer from early miscarriage or pre‐eclampsia. While the etiology of endometriosis is still unknown, abnormal accumulation of MDSCs in the peripheral blood and peritoneal fluid, alongside an increased level of reactive oxygen species (ROS), has been observed in these patients, which is central to the cellular immune regulations by MDSCs. Additionally, the regulation of MDSCs observed in tumours is also applicable to gynecologic neoplasms, including ovarian cancer and cervical cancer. More recently, emerging evidence has shown that there are high levels of MDSCs in premature ovarian failure (POF) and in vitro fertilization (IVF), but the underlying mechanisms are unknown. In this review, the generation and mechanisms of MDSCs are summarized. 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subjects | Cervical cancer Cervix Eclampsia Endometriosis Etiology Fetuses gynecologic neoplasms Gynecological diseases Gynecology Immunological tolerance In vitro fertilization miscarriage myeloid‐derived suppressor cells Ovarian cancer Peripheral blood Peritoneal fluid Peritoneum Preeclampsia Pregnancy pre‐eclampsia Reactive oxygen species Reproductive status Suppressor cells Therapeutic applications Tumors |
title | Myeloid‐derived suppressor cells in obstetrical and gynecological diseases |
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