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Human CD8+ T-Cell Populations That Express Natural Killer Receptors

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dc.contributor.authorKoh, June-Young-
dc.contributor.authorKim, Dong-Uk-
dc.contributor.authorMoon, Bae-Hyeon-
dc.contributor.authorEui-Cheol Shin-
dc.date.accessioned2023-10-18T22:03:21Z-
dc.date.available2023-10-18T22:03:21Z-
dc.date.created2023-04-03-
dc.date.issued2023-02-
dc.identifier.issn1598-2629-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/14008-
dc.description.abstractCD8+ T cells are activated by TCRs that recognize specific cognate Ags, while NK-cell activation is regulated by a balance between signals from germline-encoded activating and inhibitory NK receptors. Through these different processes of Ag recognition, CD8+ T cells and NK cells play distinct roles as adaptive and innate immune cells, respectively. However, some human CD8+ T cells have been found to express activating or inhibitory NK receptors. CD8+ T-cell populations expressing NK receptors straddle the innate-adaptive boundary with their innate-like features. Recent breakthrough technical advances in multi-omics analysis have enabled elucidation of the unique immunologic characteristics of these populations. However, studies have not yet fully clarified the heterogeneity and immunological characteristics of each CD8+ T-cell population expressing NK receptors. Here we aimed to review the current knowledge of various CD8+ T-cell populations expressing NK receptors, and to pave the way for delineating the landscape and identifying the various roles of these T-cell populations. © 2023, Korean Association of Immunologists. All rights reserved.-
dc.language영어-
dc.publisher대한면역학회-
dc.titleHuman CD8+ T-Cell Populations That Express Natural Killer Receptors-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid001042399600008-
dc.identifier.scopusid2-s2.0-85150067498-
dc.identifier.rimsid80371-
dc.contributor.affiliatedAuthorEui-Cheol Shin-
dc.identifier.doi10.4110/in.2023.23.e8-
dc.identifier.bibliographicCitationImmune Network, v.23, no.1-
dc.relation.isPartOfImmune Network-
dc.citation.titleImmune Network-
dc.citation.volume23-
dc.citation.number1-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusADHESION MOLECULE-
dc.subject.keywordPlusGAMMA-DELTA-
dc.subject.keywordPlusHUMAN LIVER-
dc.subject.keywordPlusLYMPHOCYTES-
dc.subject.keywordPlusCD94/NKG2A-
dc.subject.keywordPlusANTIGEN-
dc.subject.keywordPlusMEMORY-
dc.subject.keywordPlusBETA-
dc.subject.keywordPlusINVOLVEMENT-
dc.subject.keywordPlusPHENOTYPE-
dc.subject.keywordAuthorCD56 Antigen-
dc.subject.keywordAuthorCD8-Positive T-Lymphocytes-
dc.subject.keywordAuthorNatural Killer Cell Receptors-
dc.subject.keywordAuthorNKG2A Receptor-
dc.subject.keywordAuthorNKG2C Receptor-
dc.subject.keywordAuthorReceptors, KIR-
Appears in Collections:
Korea Virus Research Institute(한국바이러스기초연구소) > Center for Viral Immunology(바이러스 면역 연구센터) > 1. Journal Papers (저널논문)
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