Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/92039
DC FieldValueLanguage
dc.contributor.authorMendes, João-
dc.contributor.authorAreia, Ana Luísa-
dc.contributor.authorRodrigues-Santos, Paulo-
dc.contributor.authorSantos-Rosa, Manuel-
dc.contributor.authorMota-Pinto, Anabela-
dc.date.accessioned2020-12-09T10:30:05Z-
dc.date.available2020-12-09T10:30:05Z-
dc.date.issued2020-11-30-
dc.identifier.issn1664-3224-
dc.identifier.urihttps://hdl.handle.net/10316/92039-
dc.description.abstractInnate lymphoid cells (ILCs) are a new set of cells considered to be a part of the innate immune system. ILCs are classified into five subsets (according to their transcription factors and cytokine profile) as natural killer cells (NK cells), group 1 ILCs, group 2 ILCs, group 3 ILCs, and lymphoid tissue inducers (LTi). Functionally, these cells resemble the T helper population but lack the expression of recombinant genes, which is essential for the formation of T cell receptors. In this work, the authors address the distinction between peripheral and decidual NK cells, highlighting their diversity in ILC biology and its relevance to human pregnancy. ILCs are effector cells that are important in promoting immunity, inflammation, and tissue repair. Recent studies have directed their attention to ILC actions in pregnancy. Dysregulation or expansion of pro-inflammatory ILC populations as well as abnormal tolerogenic responses may directly interfere with pregnancy, ultimately resulting in pregnancy loss or adverse outcomes. In this review, we characterize these cells, considering recent findings and addressing knowledge gaps in perinatal medicine in the context of ILC biology. Moreover, we discuss the relevance of these cells not only to the process of immune tolerance, but also in disease.pt
dc.language.isoengpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectCélulas Linfoides Inataspt
dc.subjectResposta imunitária inatapt
dc.subjectInflamaçãopt
dc.subjectGravidezpt
dc.subjectParto pré-termopt
dc.subjectInflammationpt
dc.subjectInnate Lymphoid Cellspt
dc.subjectInnate immune responsept
dc.subjectPregnancypt
dc.subjectPreterm birthpt
dc.titleInnate Lymphoid Cells in Human Pregnancypt
dc.typearticlept
degois.publication.firstPage[1]pt
degois.publication.lastPage[9]pt
degois.publication.titleFrontiers in Immunologypt
dc.date.updated2020-12-03T14:37:28Z-
dc.peerreviewedyespt
dc.identifier.doi10.3389/fimmu.2020.551707-
dc.identifier.doicv-prod-2104948-
degois.publication.volume11pt
dc.description.versionF31D-D663-4EF2 | Anabela Mota Pinto-
dc.description.versioninfo:eu-repo/semantics/publishedVersion-
dc.identifier.slugcv-prod-2104948-
dc.date.embargo2020-11-30*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0003-0789-8637-
crisitem.author.orcid0000-0002-0820-9568-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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