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...

Full description

Saved in:
Bibliographic Details
Published inJournal of reproductive immunology Vol. 92; no. 1; pp. 97 - 102
Main Authors Wang, Wen-Juan, Hao, Cui-Fang, Lin, Qi-De
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ireland Ltd 01.12.2011
Elsevier
Subjects
Online AccessGet full text
ISSN0165-0378
1872-7603
1872-7603
DOI10.1016/j.jri.2011.08.004

Cover

Loading…
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.
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
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25254566$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/22015003$$D View this record in MEDLINE/PubMed
BookMark eNqFks2L1TAUxYOMOG9G_wA30o24ar3pR9IiCDJ-woALx3VIk9sxtS-tSTvY_95b31NhwJlVIPmdk9xzcsZO_OiRsaccMg5cvOyzPrgsB84zqDOA8gHb8VrmqRRQnLAdMVUKhaxP2VmMPQCX0PBH7DQnTQVQ7Fh8u8aA18ugZzf6ZOySvTZhnL7pa0y0md3N4aBdE4vG2UUPyZEfw5pcJQaHISbOJ4vHn9OgnUdLhFlCQD8nexeNDsFtdhNZ0V58zB52eoj45Lies6_v311dfEwvP3_4dPHmMjUVb-bUcATQdWkxl7pFUSLktSh1UXLNbVPLjqapse20BVvKvLVGaMiruqWTtsDinL04-E5h_LFgnNX2Gnqv9jguUTWcc0EZFfeTUAlZSZET-exILu0erZqC2-uwqj-JEvD8CGiafOiC9sbFf1yVV2UlBHH8wFHakSro_iIc1Nau6hW1q7Z2FdSK2iWNvKUxbv7dzxy0G-5UvjookfK-cRhUNNSFQeuoq1nZ0d2pfn1LbQbnHY33HVeM_bgET0UqrmKuQH3Z_t327TinRAAkGTT_N7jn8l_r7Ogo
CODEN JRIMDR
CitedBy_id crossref_primary_10_1071_RD15489
crossref_primary_10_1111_jog_15907
crossref_primary_10_3389_fimmu_2014_00253
crossref_primary_10_1016_j_lfs_2022_120503
crossref_primary_10_3389_fimmu_2019_00792
crossref_primary_10_1016_j_jri_2014_09_053
crossref_primary_10_3390_ijms20215332
crossref_primary_10_1007_s00005_019_00552_7
crossref_primary_10_3389_fimmu_2020_01898
crossref_primary_10_3389_fimmu_2023_1082087
crossref_primary_10_1177_1933719116675054
crossref_primary_10_1093_biolre_ioac030
crossref_primary_10_1111_aji_12357
crossref_primary_10_1016_j_placenta_2019_03_003
crossref_primary_10_1016_j_jri_2012_06_002
crossref_primary_10_1111_aji_12791
crossref_primary_10_3390_ijms24065300
crossref_primary_10_3389_fimmu_2019_01550
crossref_primary_10_1080_14647273_2018_1524935
crossref_primary_10_3389_fimmu_2021_691908
crossref_primary_10_3389_fimmu_2014_00606
crossref_primary_10_3389_fimmu_2024_1379537
crossref_primary_10_1038_cmi_2014_36
crossref_primary_10_3389_fendo_2022_1023194
crossref_primary_10_1371_journal_pone_0129110
crossref_primary_10_3389_fimmu_2022_994888
crossref_primary_10_1016_j_jri_2020_103264
crossref_primary_10_1016_j_jri_2022_103785
crossref_primary_10_1016_j_jri_2012_12_001
crossref_primary_10_3389_fgwh_2022_820759
crossref_primary_10_1016_j_intimp_2023_110326
crossref_primary_10_1016_j_placenta_2022_10_007
crossref_primary_10_3389_fimmu_2020_557184
crossref_primary_10_3390_ijms23116113
crossref_primary_10_1111_pim_12606
crossref_primary_10_3109_14767058_2015_1039507
crossref_primary_10_3389_fimmu_2022_1045532
crossref_primary_10_1038_s41419_019_1380_0
crossref_primary_10_1093_molehr_gaaa035
crossref_primary_10_3389_fimmu_2019_02317
crossref_primary_10_14411_fp_2022_020
crossref_primary_10_1016_j_jri_2022_103754
crossref_primary_10_1016_j_intimp_2020_106981
crossref_primary_10_1016_j_jri_2022_103750
crossref_primary_10_1111_aji_12329
crossref_primary_10_3389_fimmu_2020_00458
crossref_primary_10_1016_j_micpath_2018_08_043
crossref_primary_10_1111_aji_12531
crossref_primary_10_1016_j_jgyn_2012_07_001
crossref_primary_10_1093_humrep_deu043
crossref_primary_10_3390_ijms24010132
crossref_primary_10_1007_s43032_023_01436_0
crossref_primary_10_1097_CM9_0000000000003114
crossref_primary_10_1080_09513590_2016_1212829
crossref_primary_10_1016_j_jri_2023_103942
crossref_primary_10_1038_s41398_021_01498_1
crossref_primary_10_1016_j_tjog_2022_06_014
Cites_doi 10.1038/ni1109-1141
10.1016/j.jri.2003.10.004
10.1084/jem.193.11.1295
10.1038/39614
10.1016/j.jri.2004.08.009
10.1073/pnas.0706832104
10.1084/jem.193.11.1285
10.1006/exer.2001.1109
10.1016/S1074-7613(00)80014-X
10.1097/00007890-199803270-00012
10.1016/j.humimm.2004.12.006
10.1016/j.jri.2009.12.003
10.1111/j.1600-0897.2009.00689.x
10.1084/jem.190.7.995
10.1093/humrep/deq198
10.1051/rnd:19881006
10.1038/ni.1791
10.1097/00007890-199511270-00019
ContentType Journal Article
Copyright 2011 Elsevier Ireland Ltd
Elsevier Ireland Ltd
2015 INIST-CNRS
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
Copyright_xml – notice: 2011 Elsevier Ireland Ltd
– notice: Elsevier Ireland Ltd
– notice: 2015 INIST-CNRS
– notice: Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
DBID AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7T5
H94
DOI 10.1016/j.jri.2011.08.004
DatabaseName CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
Immunology Abstracts
AIDS and Cancer Research Abstracts
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
AIDS and Cancer Research Abstracts
Immunology Abstracts
DatabaseTitleList MEDLINE - Academic

AIDS and Cancer Research Abstracts
MEDLINE


Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Pharmacy, Therapeutics, & Pharmacology
EISSN 1872-7603
EndPage 102
ExternalDocumentID 22015003
25254566
10_1016_j_jri_2011_08_004
S0165037811003007
1_s2_0_S0165037811003007
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
--K
--M
.1-
.FO
.GJ
.~1
0R~
1B1
1P~
1RT
1~.
1~5
29L
4.4
457
4G.
53G
5GY
5RE
5VS
7-5
71M
8P~
9JM
AAAJQ
AAEDT
AAEDW
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AAQXK
AARKO
AATTM
AAXKI
AAXUO
AAYWO
ABBQC
ABFNM
ABJNI
ABMAC
ABMZM
ABWVN
ABXDB
ACDAQ
ACGFS
ACIEU
ACIUM
ACRLP
ACRPL
ACVFH
ADBBV
ADCNI
ADEZE
ADMUD
ADNMO
AEBSH
AEIPS
AEKER
AENEX
AEUPX
AEVXI
AFJKZ
AFPUW
AFRHN
AFTJW
AFXIZ
AGCQF
AGEKW
AGHFR
AGQPQ
AGUBO
AGYEJ
AHHHB
AIEXJ
AIGII
AIIUN
AIKHN
AITUG
AJRQY
AJUYK
AKBMS
AKRWK
AKYEP
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
ANKPU
ANZVX
APXCP
ASPBG
AVWKF
AXJTR
AZFZN
BKOJK
BLXMC
BNPGV
CJTIS
CNWQP
CS3
DU5
EBS
EFJIC
EFKBS
EJD
EO8
EO9
EP2
EP3
F5P
FDB
FEDTE
FGOYB
FIRID
FNPLU
FYGXN
G-2
G-Q
GBLVA
HDU
HMG
HMK
HMO
HVGLF
HZ~
IHE
J1W
KOM
LUGTX
M29
M41
MO0
N9A
O-L
O9-
OAUVE
OQ.
OZT
P-8
P-9
P2P
PC.
PH~
Q38
R2-
ROL
RPZ
SAE
SDF
SDG
SEL
SES
SEW
SIN
SPCBC
SSH
SSI
SSZ
T5K
UHS
WUQ
Z5R
ZGI
~G-
AACTN
AFCTW
AFKWA
AJOXV
AMFUW
RIG
AAIAV
ABLVK
ABYKQ
AJBFU
EFLBG
LCYCR
AAYXX
AGRNS
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7T5
H94
ID FETCH-LOGICAL-c519t-c1e00a84de27abe64e02864a341a1d987f7098ebfad0d472bdc6a0258b7f7b3e3
IEDL.DBID .~1
ISSN 0165-0378
1872-7603
IngestDate Fri Jul 11 08:38:20 EDT 2025
Thu Jul 10 18:31:56 EDT 2025
Mon Jul 21 05:56:41 EDT 2025
Mon Jul 21 09:14:02 EDT 2025
Tue Jul 01 01:26:19 EDT 2025
Thu Apr 24 22:59:48 EDT 2025
Fri Feb 23 02:21:40 EST 2024
Sun Feb 23 10:18:57 EST 2025
Tue Aug 26 16:31:54 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 1
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
License https://www.elsevier.com/tdm/userlicense/1.0
CC BY 4.0
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c519t-c1e00a84de27abe64e02864a341a1d987f7098ebfad0d472bdc6a0258b7f7b3e3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Article-2
ObjectType-Feature-1
PMID 22015003
PQID 905675762
PQPubID 23479
PageCount 6
ParticipantIDs proquest_miscellaneous_911160163
proquest_miscellaneous_905675762
pubmed_primary_22015003
pascalfrancis_primary_25254566
crossref_primary_10_1016_j_jri_2011_08_004
crossref_citationtrail_10_1016_j_jri_2011_08_004
elsevier_sciencedirect_doi_10_1016_j_jri_2011_08_004
elsevier_clinicalkeyesjournals_1_s2_0_S0165037811003007
elsevier_clinicalkey_doi_10_1016_j_jri_2011_08_004
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2011-12-01
PublicationDateYYYYMMDD 2011-12-01
PublicationDate_xml – month: 12
  year: 2011
  text: 2011-12-01
  day: 01
PublicationDecade 2010
PublicationPlace Kidlington
PublicationPlace_xml – name: Kidlington
– name: Ireland
PublicationTitle Journal of reproductive immunology
PublicationTitleAlternate J Reprod Immunol
PublicationYear 2011
Publisher Elsevier Ireland Ltd
Elsevier
Publisher_xml – name: Elsevier Ireland Ltd
– name: Elsevier
References Levings, Sangregorio, Roncarolo (bib0060) 2001; 193
Asseman, Mauze, Leach, Coffman, Powrie (bib0005) 1999; 190
Bulmer, Pace, Ritson (bib0010) 1988; 28
Groux, O’Garra, Bigler, Rouleau, Antonenko, de Vries, Roncarolo (bib0025) 1997; 389
Kano, Bashuda, Yagita, Okumura, Morishita (bib0045) 1998; 65
Jin, Wang, Xiao, Lv, Ding, Lin (bib0035) 2009; 61
World Health Organization, 2010. WHO Laboratory Manual for the Examination and Processing of Human Semen.
Goerdt, Orfanos (bib0020) 1999; 10
Wang, Hao, Yi-Lin, Yin, Bao, Qiu, Lin (bib0085) 2010; 84
Kagaya, Hori, Kamiya, Kaji, Oshika, Amano, Yamagami, Tsuru, Tanaka, Matsuda, Yagita, Okumura (bib0050) 2002; 74
Jin, Zhou, Wang, Zhu, Li (bib0030) 2005; 65
Lenschow, ZengY, Hathcock, Zuckerman, Freeman, Thistlethwaite, Gray, Hodes, Bluestone (bib0055) 1995; 60
Daher, de Arruda Geraldes Denardi, Blotta, Mamoni, Reck, Camano, Mattar (bib0015) 2004; 62
Murai, Turovskaya, Kim, Madan, Karp, Cheroutre, Kronenberg (bib0065) 2009; 10
Taams, van Amelsfort, Tiemessen, Jacobs, de Jong, Akbar, Bijlsma, Lafeber (bib0070) 2005; 66
Unutmaz, Pulendran (bib0080) 2009; 10
Jonuleit, Schmitt, Stassen, Tuettenberg, Knop, Enk (bib0040) 2001; 193
Tiemessen, Jagger, Evans, van Herwijnen, John, Taams (bib0075) 2007; 104
Wang, Hao, Qu, Wang, Qiu, Lin (bib0090) 2010; 25
Levings (10.1016/j.jri.2011.08.004_bib0060) 2001; 193
Jin (10.1016/j.jri.2011.08.004_bib0030) 2005; 65
Groux (10.1016/j.jri.2011.08.004_bib0025) 1997; 389
Unutmaz (10.1016/j.jri.2011.08.004_bib0080) 2009; 10
Kano (10.1016/j.jri.2011.08.004_bib0045) 1998; 65
Tiemessen (10.1016/j.jri.2011.08.004_bib0075) 2007; 104
Jonuleit (10.1016/j.jri.2011.08.004_bib0040) 2001; 193
Wang (10.1016/j.jri.2011.08.004_bib0090) 2010; 25
Goerdt (10.1016/j.jri.2011.08.004_bib0020) 1999; 10
Wang (10.1016/j.jri.2011.08.004_bib0085) 2010; 84
Daher (10.1016/j.jri.2011.08.004_bib0015) 2004; 62
Kagaya (10.1016/j.jri.2011.08.004_bib0050) 2002; 74
Jin (10.1016/j.jri.2011.08.004_bib0035) 2009; 61
Lenschow (10.1016/j.jri.2011.08.004_bib0055) 1995; 60
Murai (10.1016/j.jri.2011.08.004_bib0065) 2009; 10
Asseman (10.1016/j.jri.2011.08.004_bib0005) 1999; 190
Taams (10.1016/j.jri.2011.08.004_bib0070) 2005; 66
10.1016/j.jri.2011.08.004_bib0095
Bulmer (10.1016/j.jri.2011.08.004_bib0010) 1988; 28
References_xml – volume: 190
  start-page: 995
  year: 1999
  end-page: 1004
  ident: bib0005
  article-title: An essential role for interleukin-10 in the function of regulatory T cells that inhibit intestinal inflammation
  publication-title: J. Exp. Med.
– volume: 28
  start-page: 1599
  year: 1988
  end-page: 1613
  ident: bib0010
  article-title: Immunoregulatory cells in human decidua: morphology, immunohistochemistry and function
  publication-title: Reprod. Nutr. Dev.
– volume: 10
  start-page: 1141
  year: 2009
  end-page: 1143
  ident: bib0080
  article-title: The gut feeling of Treg cells: IL10 is the silver lining during colitis
  publication-title: Nat. Immunol.
– volume: 61
  start-page: 253
  year: 2009
  end-page: 260
  ident: bib0035
  article-title: The role of TSP-1 on decidual macrophages involved in the susceptibility to unexplained recurrent spontaneous abortion
  publication-title: Am. J. Reprod. Immunol.
– volume: 66
  start-page: 222
  year: 2005
  end-page: 230
  ident: bib0070
  article-title: Modulation of monocyte/macrophage function by human CD4+CD25+ regulatory T cells
  publication-title: Hum. Immunol.
– volume: 10
  start-page: 137
  year: 1999
  end-page: 142
  ident: bib0020
  article-title: Other functions, other genes: alternative activation of antigen-presenting cells
  publication-title: Immunity
– volume: 62
  start-page: 151
  year: 2004
  end-page: 157
  ident: bib0015
  article-title: Cytokines in recurrent pregnancy loss
  publication-title: J. Reprod. Immunol.
– volume: 74
  start-page: 131
  year: 2002
  end-page: 139
  ident: bib0050
  article-title: Inhibition of murine corneal allograft rejection by treatment with antibodies to CD80 and CD86
  publication-title: Exp. Eye Res.
– volume: 84
  start-page: 164
  year: 2010
  end-page: 170
  ident: bib0085
  article-title: Increased prevalence of T helper 17 (Th17) cells in peripheral blood and decidua in unexplained recurrent miscarriage patients
  publication-title: J. Reprod. Immunol.
– volume: 104
  start-page: 19446
  year: 2007
  end-page: 19451
  ident: bib0075
  article-title: CD4+CD25+Foxp3+ regulatory T cells induce alternative activation of human monocytes/macrophages
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
– volume: 25
  start-page: 2591
  year: 2010
  end-page: 2596
  ident: bib0090
  article-title: The deregulation of regulatory T cells on interleukin-17-producing T helper cells in patients with unexplained early recurrent miscarriage
  publication-title: Hum. Reprod.
– volume: 60
  start-page: 1171
  year: 1995
  end-page: 1178
  ident: bib0055
  article-title: Inhibition of transplant rejection following treatment with anti-B7-2 and anti-B7-1 antibodies
  publication-title: Transplantation
– volume: 193
  start-page: 1285
  year: 2001
  end-page: 1294
  ident: bib0040
  article-title: Identification and functional characterization of human CD4+CD25+ T cells with regulatory properties isolated from peripheral blood
  publication-title: J. Exp. Med.
– volume: 193
  start-page: 1295
  year: 2001
  end-page: 1301
  ident: bib0060
  article-title: Human CD25+CD4+ T regulatory cells suppress naive and memory T cell proliferation and can be expanded in vitro without loss of function
  publication-title: J. Exp. Med.
– volume: 65
  start-page: 133
  year: 2005
  end-page: 146
  ident: bib0030
  article-title: Blockade of CD80 and CD86 at the time of implantation inhibits maternal rejection to the allogeneic fetus in abortion-prone matings
  publication-title: J. Reprod. Immunol.
– volume: 389
  start-page: 737
  year: 1997
  end-page: 742
  ident: bib0025
  article-title: A CD4+ T-cell subset inhibits antigen-specific T-cell responses and prevents colitis
  publication-title: Nature
– reference: World Health Organization, 2010. WHO Laboratory Manual for the Examination and Processing of Human Semen.
– volume: 65
  start-page: 837
  year: 1998
  end-page: 843
  ident: bib0045
  article-title: A crucial role of host CD80 and CD86 in rat cardiac xenograft rejection in mice
  publication-title: Transplantation
– volume: 10
  start-page: 1178
  year: 2009
  end-page: 1184
  ident: bib0065
  article-title: Interleukin 10 acts on regulatory T cells to maintain expression of the transcription factor Foxp3 and suppressive function in mice with colitis
  publication-title: Nat. Immunol.
– volume: 10
  start-page: 1141
  year: 2009
  ident: 10.1016/j.jri.2011.08.004_bib0080
  article-title: The gut feeling of Treg cells: IL10 is the silver lining during colitis
  publication-title: Nat. Immunol.
  doi: 10.1038/ni1109-1141
– volume: 62
  start-page: 151
  year: 2004
  ident: 10.1016/j.jri.2011.08.004_bib0015
  article-title: Cytokines in recurrent pregnancy loss
  publication-title: J. Reprod. Immunol.
  doi: 10.1016/j.jri.2003.10.004
– volume: 193
  start-page: 1295
  year: 2001
  ident: 10.1016/j.jri.2011.08.004_bib0060
  article-title: Human CD25+CD4+ T regulatory cells suppress naive and memory T cell proliferation and can be expanded in vitro without loss of function
  publication-title: J. Exp. Med.
  doi: 10.1084/jem.193.11.1295
– volume: 389
  start-page: 737
  year: 1997
  ident: 10.1016/j.jri.2011.08.004_bib0025
  article-title: A CD4+ T-cell subset inhibits antigen-specific T-cell responses and prevents colitis
  publication-title: Nature
  doi: 10.1038/39614
– volume: 65
  start-page: 133
  year: 2005
  ident: 10.1016/j.jri.2011.08.004_bib0030
  article-title: Blockade of CD80 and CD86 at the time of implantation inhibits maternal rejection to the allogeneic fetus in abortion-prone matings
  publication-title: J. Reprod. Immunol.
  doi: 10.1016/j.jri.2004.08.009
– volume: 104
  start-page: 19446
  year: 2007
  ident: 10.1016/j.jri.2011.08.004_bib0075
  article-title: CD4+CD25+Foxp3+ regulatory T cells induce alternative activation of human monocytes/macrophages
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.0706832104
– volume: 193
  start-page: 1285
  year: 2001
  ident: 10.1016/j.jri.2011.08.004_bib0040
  article-title: Identification and functional characterization of human CD4+CD25+ T cells with regulatory properties isolated from peripheral blood
  publication-title: J. Exp. Med.
  doi: 10.1084/jem.193.11.1285
– volume: 74
  start-page: 131
  year: 2002
  ident: 10.1016/j.jri.2011.08.004_bib0050
  article-title: Inhibition of murine corneal allograft rejection by treatment with antibodies to CD80 and CD86
  publication-title: Exp. Eye Res.
  doi: 10.1006/exer.2001.1109
– volume: 10
  start-page: 137
  year: 1999
  ident: 10.1016/j.jri.2011.08.004_bib0020
  article-title: Other functions, other genes: alternative activation of antigen-presenting cells
  publication-title: Immunity
  doi: 10.1016/S1074-7613(00)80014-X
– volume: 65
  start-page: 837
  year: 1998
  ident: 10.1016/j.jri.2011.08.004_bib0045
  article-title: A crucial role of host CD80 and CD86 in rat cardiac xenograft rejection in mice
  publication-title: Transplantation
  doi: 10.1097/00007890-199803270-00012
– volume: 66
  start-page: 222
  year: 2005
  ident: 10.1016/j.jri.2011.08.004_bib0070
  article-title: Modulation of monocyte/macrophage function by human CD4+CD25+ regulatory T cells
  publication-title: Hum. Immunol.
  doi: 10.1016/j.humimm.2004.12.006
– volume: 84
  start-page: 164
  year: 2010
  ident: 10.1016/j.jri.2011.08.004_bib0085
  article-title: Increased prevalence of T helper 17 (Th17) cells in peripheral blood and decidua in unexplained recurrent miscarriage patients
  publication-title: J. Reprod. Immunol.
  doi: 10.1016/j.jri.2009.12.003
– volume: 61
  start-page: 253
  year: 2009
  ident: 10.1016/j.jri.2011.08.004_bib0035
  article-title: The role of TSP-1 on decidual macrophages involved in the susceptibility to unexplained recurrent spontaneous abortion
  publication-title: Am. J. Reprod. Immunol.
  doi: 10.1111/j.1600-0897.2009.00689.x
– ident: 10.1016/j.jri.2011.08.004_bib0095
– volume: 190
  start-page: 995
  year: 1999
  ident: 10.1016/j.jri.2011.08.004_bib0005
  article-title: An essential role for interleukin-10 in the function of regulatory T cells that inhibit intestinal inflammation
  publication-title: J. Exp. Med.
  doi: 10.1084/jem.190.7.995
– volume: 25
  start-page: 2591
  year: 2010
  ident: 10.1016/j.jri.2011.08.004_bib0090
  article-title: The deregulation of regulatory T cells on interleukin-17-producing T helper cells in patients with unexplained early recurrent miscarriage
  publication-title: Hum. Reprod.
  doi: 10.1093/humrep/deq198
– volume: 28
  start-page: 1599
  year: 1988
  ident: 10.1016/j.jri.2011.08.004_bib0010
  article-title: Immunoregulatory cells in human decidua: morphology, immunohistochemistry and function
  publication-title: Reprod. Nutr. Dev.
  doi: 10.1051/rnd:19881006
– volume: 10
  start-page: 1178
  year: 2009
  ident: 10.1016/j.jri.2011.08.004_bib0065
  article-title: Interleukin 10 acts on regulatory T cells to maintain expression of the transcription factor Foxp3 and suppressive function in mice with colitis
  publication-title: Nat. Immunol.
  doi: 10.1038/ni.1791
– volume: 60
  start-page: 1171
  year: 1995
  ident: 10.1016/j.jri.2011.08.004_bib0055
  article-title: Inhibition of transplant rejection following treatment with anti-B7-2 and anti-B7-1 antibodies
  publication-title: Transplantation
  doi: 10.1097/00007890-199511270-00019
SSID ssj0017091
Score 2.2380102
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...
SourceID proquest
pubmed
pascalfrancis
crossref
elsevier
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 97
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
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0165037811003007
https://www.clinicalkey.es/playcontent/1-s2.0-S0165037811003007
https://dx.doi.org/10.1016/j.jri.2011.08.004
https://www.ncbi.nlm.nih.gov/pubmed/22015003
https://www.proquest.com/docview/905675762
https://www.proquest.com/docview/911160163
Volume 92
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3Pa9swFBaluwzG2O953YIOo4dRL7KsyPaxdCvZxkphKfQmJFleU4ptrATqy_72PVlyQlmXwQ65xE-OIn1-74vyvvcQel8wM8s5Z3HOlIoZT1Pwg6mJjeYqobJgM-IEzt_P-PyCfb2cXe6hk1EL49Iqg-_3Pn3w1uGdaVjNabtcTn84IQ5JnVLSIXVQlDOWOZR__LVJ80gy4rvmgXHsrMd_Noccr-tuua3iGXq13RObHrXSwopVvtXF37noEJNOn6DHgUziYz_fp2jP1M_Q4bmvRt0f4cVWXGWP8CE-39ap7p8j-6mHOfwM_btwU2G41jXtFbgY7PQO_rQWqx6XRg-iLRzsm67HC-wO_S1e1nhdm9v2RgJhLcFC-5JPGBCkZQcAh9uF8q32Bbo4_bw4mcehB0OsgdutYp0YQmTOSkMzqQxnBggJZxKCn0zKIs8qWODcqEqWpGQZVaXmEnhUruCKSk36Eu3XTW1eIwxkJqdFaVhVwAvosqJVCe6VsyrRpMoiRMbVFzoUKHd9Mm7EmIl2LWDDhNsw4XpnEhahD5shra_OscuYjlsqRtkpOEoBsWPXoOy-QcaGR92KRFgqiPgDjhFim5F3EP2vD5zcQdvme9EZdWyXRwiP8BNuI12SXG2atRUFkNkMfj_SHSYQ2lwBnjRCrzxyt_en7vCLpG_-b94H6OFw3D5k-rxF-6tubd4BX1upyfBATtCD4y_f5me_AXnHQPw
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3da9swED9K-rDBGPue99HpYfRh1ESWZdl-LN1KurahsBT6JiRb7lKKHewE6v--J1tOKOsy2INf4jtbkc53P8v3uwP4mnITJUJwP-Fa-1yEIfrB0PgmEzpgKuURtQTn86mYXPKfV9HVDhwNXBibVul8f-_TO2_tfhm72Rwv5vPxL0vEoaFlSlpLtYzyXVudKhrB7uHJ6WS6_pgQ075xHsr7VmH4uNmled3U800hT9eu7ZHw9GyhGpy0ou928Xc42oWl4xfw3OFJctgP-SXsmPIV7F_0BanbAzLb8KuaA7JPLjalqtvX0HxvcQzXroUXqQqC5-pq8Ru9DLGUh37DluiW5CbreFvEyVd1S2bE7vs3ZF6SVWnuFrcKMWuOEllf9YmgEWWqRhvHy7kKrs0buDz-MTua-K4Ng58hvFv6WWAoVQnPDYuVNoIbxCSCK4x_KsjTJC5wghOjC5XTnMdM55lQCKUSjWd0aMK3MCqr0rwHgngmYWlueJHigYhZsyJHDyt4EWS0iD2gw-zLzNUot60ybuWQjHYjccGkXTBp22dS7sG3tcqiL9CxTZgNSyoH5in6SonhY5tS_JiSadzT3shANkxS-YdFesDXmg-M-l833Htgbev_xSJmAa_wgAzmJ-1C2jy50lSrRqaIZ2N8hWRbRDC62Ro8oQfvesvdXJ_Z_S8afvi_cX-BJ5PZ-Zk8O5mefoSn3e57l_jzCUbLemU-I3xb6j33eN4DUTFDrQ
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Dysregulation+of+macrophage+activation+by+decidual+regulatory+T+cells+in+unexplained+recurrent+miscarriage+patients&rft.jtitle=Journal+of+reproductive+immunology&rft.au=Wang%2C+Wen-Juan&rft.au=Hao%2C+Cui-Fang&rft.au=Lin%2C+Qi-De&rft.date=2011-12-01&rft.issn=0165-0378&rft.volume=92&rft.issue=1&rft.spage=97&rft.epage=102&rft_id=info:doi/10.1016%2Fj.jri.2011.08.004&rft.externalDBID=ECK1-s2.0-S0165037811003007&rft.externalDocID=1_s2_0_S0165037811003007
thumbnail_m http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F01650378%2FS0165037811X00086%2Fcov150h.gif