001     139339
005     20240321220612.0
024 7 _ |a 10.1038/nature22795
|2 doi
024 7 _ |a pmid:28614294
|2 pmid
024 7 _ |a pmc:PMC6588541
|2 pmc
024 7 _ |a 0028-0836
|2 ISSN
024 7 _ |a 1476-4687
|2 ISSN
024 7 _ |a altmetric:21064280
|2 altmetric
037 _ _ |a DZNE-2020-05661
041 _ _ |a English
082 _ _ |a 500
100 1 _ |a McGovern, Naomi
|b 0
245 _ _ |a Human fetal dendritic cells promote prenatal T-cell immune suppression through arginase-2.
260 _ _ |a London [u.a.]
|c 2017
|b Nature Publ. Group65848
264 _ 1 |3 online
|2 Crossref
|b Springer Science and Business Media LLC
|c 2017-06-14
264 _ 1 |3 print
|2 Crossref
|b Springer Science and Business Media LLC
|c 2017-06-01
336 7 _ |a article
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336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a During gestation the developing human fetus is exposed to a diverse range of potentially immune-stimulatory molecules including semi-allogeneic antigens from maternal cells, substances from ingested amniotic fluid, food antigens, and microbes. Yet the capacity of the fetal immune system, including antigen-presenting cells, to detect and respond to such stimuli remains unclear. In particular, dendritic cells, which are crucial for effective immunity and tolerance, remain poorly characterized in the developing fetus. Here we show that subsets of antigen-presenting cells can be identified in fetal tissues and are related to adult populations of antigen-presenting cells. Similar to adult dendritic cells, fetal dendritic cells migrate to lymph nodes and respond to toll-like receptor ligation; however, they differ markedly in their response to allogeneic antigens, strongly promoting regulatory T-cell induction and inhibiting T-cell tumour-necrosis factor-α production through arginase-2 activity. Our results reveal a previously unappreciated role of dendritic cells within the developing fetus and indicate that they mediate homeostatic immune-suppressive responses during gestation.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
|0 G:(DE-HGF)POF3-342
|c POF3-342
|f POF III
|x 0
542 _ _ |i 2017-06-01
|2 Crossref
|u http://www.springer.com/tdm
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Cytokines
|2 NLM Chemicals
650 _ 7 |a Toll-Like Receptors
|2 NLM Chemicals
650 _ 7 |a Arginase
|0 EC 3.5.3.1
|2 NLM Chemicals
650 _ 7 |a arginase II, human
|0 EC 3.5.3.1
|2 NLM Chemicals
650 _ 2 |a Adult
|2 MeSH
650 _ 2 |a Arginase: metabolism
|2 MeSH
650 _ 2 |a Cell Movement
|2 MeSH
650 _ 2 |a Cell Proliferation
|2 MeSH
650 _ 2 |a Cytokines: biosynthesis
|2 MeSH
650 _ 2 |a Cytokines: immunology
|2 MeSH
650 _ 2 |a Dendritic Cells: enzymology
|2 MeSH
650 _ 2 |a Dendritic Cells: immunology
|2 MeSH
650 _ 2 |a Fetus: cytology
|2 MeSH
650 _ 2 |a Fetus: enzymology
|2 MeSH
650 _ 2 |a Fetus: immunology
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Immune Tolerance
|2 MeSH
650 _ 2 |a Lymph Nodes: cytology
|2 MeSH
650 _ 2 |a Lymph Nodes: immunology
|2 MeSH
650 _ 2 |a T-Lymphocytes: cytology
|2 MeSH
650 _ 2 |a T-Lymphocytes: immunology
|2 MeSH
650 _ 2 |a T-Lymphocytes, Regulatory: cytology
|2 MeSH
650 _ 2 |a T-Lymphocytes, Regulatory: immunology
|2 MeSH
650 _ 2 |a Toll-Like Receptors: immunology
|2 MeSH
700 1 _ |a Shin, Amanda
|b 1
700 1 _ |a Low, Gillian
|b 2
700 1 _ |a Low, Donovan
|b 3
700 1 _ |a Duan, Kaibo
|b 4
700 1 _ |a Yao, Leong Jing
|b 5
700 1 _ |a Msallam, Rasha
|b 6
700 1 _ |a Low, Ivy
|b 7
700 1 _ |a Shadan, Nurhidaya Binte
|b 8
700 1 _ |a Sumatoh, Hermi R
|b 9
700 1 _ |a Soon, Erin
|b 10
700 1 _ |a Lum, Josephine
|b 11
700 1 _ |a Mok, Esther
|b 12
700 1 _ |a Hubert, Sandra
|b 13
700 1 _ |a See, Peter
|b 14
700 1 _ |a Kunxiang, Edwin Huang
|b 15
700 1 _ |a Lee, Yie Hou
|b 16
700 1 _ |a Janela, Baptiste
|b 17
700 1 _ |a Choolani, Mahesh
|b 18
700 1 _ |a Mattar, Citra Nurfarah Zaini
|b 19
700 1 _ |a Fan, Yiping
|b 20
700 1 _ |a Lim, Tony Kiat Hon
|b 21
700 1 _ |a Chan, Dedrick Kok Hong
|b 22
700 1 _ |a Tan, Ker-Kan
|b 23
700 1 _ |a Tam, John Kit Chung
|b 24
700 1 _ |a Schuster, Christopher
|b 25
700 1 _ |a Elbe-Bürger, Adelheid
|b 26
700 1 _ |a Wang, Xiao-Nong
|b 27
700 1 _ |a Bigley, Venetia
|b 28
700 1 _ |a Collin, Matthew
|b 29
700 1 _ |a Haniffa, Muzlifah
|b 30
700 1 _ |a Schlitzer, Andreas
|0 P:(DE-2719)2813805
|b 31
|u dzne
700 1 _ |a Poidinger, Michael
|b 32
700 1 _ |a Albani, Salvatore
|b 33
700 1 _ |a Larbi, Anis
|b 34
700 1 _ |a Newell, Evan W
|b 35
700 1 _ |a Chan, Jerry Kok Yen
|b 36
700 1 _ |a Ginhoux, Florent
|0 P:(DE-HGF)0
|b 37
|e Corresponding author
773 1 8 |a 10.1038/nature22795
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|n 7660
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|v 546
|y 2017
|x 0028-0836
773 _ _ |a 10.1038/nature22795
|g Vol. 546, no. 7660, p. 662 - 666
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909 C O |o oai:pub.dzne.de:139339
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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913 1 _ |a DE-HGF
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21