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Review Immune network. 2023 Feb 20;23(1):e8. doi: 10.4110/in.2023.23.e8 Q24.32024

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

表达自然杀伤细胞受体的人类CD8+t细胞群体 翻译改进

June-Young Koh  1  2, Dong-Uk Kim  1, Bae-Hyeon Moon  1, Eui-Cheol Shin  1  3

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作者单位

  • 1 Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Korea.
  • 2 Genome Insight, Inc., Daejeon 34051, Korea.
  • 3 The Center for Viral Immunology, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Korea.
  • DOI: 10.4110/in.2023.23.e8 PMID: 36911797

    摘要 Ai翻译

    CD8+ 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.

    Keywords: CD56 Antigen; CD8-Positive T-Lymphocytes; NKG2A Receptor; NKG2C Receptor; Natural Killer Cell Receptors; Receptors, KIR.

    Keywords:human cd8+; t-cell populations; natural killer receptors

    Copyright © Immune network. 中文内容为AI机器翻译,仅供参考!

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    期刊名:Immune network

    缩写:IMMUNE NETW

    ISSN:1598-2629

    e-ISSN:2092-6685

    IF/分区:4.3/Q2

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