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  • 标题:Crosstalk between decidual NK and CD14+ myelomonocytic cells results in induction of Tregs and immunosuppression
  • 本地全文:下载
  • 作者:Paola Vacca ; Claudia Cantoni ; Massimo Vitale
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2010
  • 卷号:107
  • 期号:26
  • 页码:11918-11923
  • DOI:10.1073/pnas.1001749107
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Regulatory T cells (Tregs) are thought to play a major role in pregnancy by inhibiting the maternal immune system and preventing fetal rejection. In decidual tissues, NK cells (dNK) reside in close contact with particular myelomonocytic CD14+ (dCD14+) cells. Here we show that the interaction between dNK and dCD14+ cells results in induction of Tregs. The interaction is mediated by soluble factors as shown by transwell experiments, and the prominent role of IFN-{gamma} is revealed by the effect of a neutralizing monoclonal antibody. Following interaction with dNK cells, dCD14+ cells express indoleamine 2,3-dioxygenase (IDO), which, in turn, induces Tregs. Notably, unlike peripheral blood NK (pNK) cells, dNK cells are resistant to inhibition by the IDO metabolite L-kynurenine. "Conditioned" dCD14+ cells also may induce Tregs through transforming growth factor-{beta} (TGF-{beta}) production or CTLA-4-mediated interactions, as indicated by the effect of specific neutralizing Abs. Remarkably, only the interaction between dNK and dCD14+ cells results in Treg induction, whereas other coculture combinations involving either NK or CD14+ cells isolated from peripheral blood are ineffective. Our study provides interesting clues to understanding how the crosstalk between decidual NK and CD14+ cells may initiate a process that leads to Treg induction and immunosuppression. Along this line, it is conceivable that an impaired function of these cells may result in pregnancy failure.
  • 关键词:indoleamine 2,3-dioxygenase ; regulatory T cells ; tolerance in pregnancy ; transforming growth factor β
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