Suppr超能文献

人 γδ T 细胞对 CD1 和 MR1 的识别。

CD1 and MR1 recognition by human γδ T cells.

机构信息

Brigham and Women's Hospital, Division of Rheumatology, Inflammation and Immunity, and Harvard Medical School, Boston, MA, 02115, USA; Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, 3584CL, Utrecht, The Netherlands.

Infection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, 3800, Australia; Australian Research Council Centre of Excellence in Advanced Molecular Imaging, Monash University, Clayton, Victoria, 3800, Australia.

出版信息

Mol Immunol. 2021 May;133:95-100. doi: 10.1016/j.molimm.2020.12.008. Epub 2021 Feb 23.

Abstract

The two main T cell lineages, αβ and γδ T cells, play a central role in immunity. Unlike αβ T cells that recognize antigens bound to the Major Histocompatibility Complex (MHC) or MHC class I-like antigen-presenting molecules, the ligands for γδ T cell receptors (TCRs) are much more diverse. However, it is now clear that γδ TCRs can also recognize MHC class I-like molecules, including CD1b, CD1c, CD1d and the MHC class I-related protein 1 (MR1). Yet, our understanding at the molecular level of γδ T cell immunity to CD1 and MR1 is still very limited. Here, we discuss new molecular paradigms underpinning γδ TCRs recognition of antigens, antigen-presenting molecules or both. The recent discovery of recognition of MR1 by a γδ TCR at a position located underneath the antigen display platform reinforces the view that γδ TCRs can approach their ligands from many directions, unlike αβ TCRs that bind MHC, CD1 and MR1 targets in an aligned, end to end fashion.

摘要

两种主要的 T 细胞谱系,αβ 和 γδ T 细胞,在免疫中发挥核心作用。与识别与主要组织相容性复合体 (MHC) 或 MHC 类样抗原呈递分子结合的抗原的 αβ T 细胞不同,γδ T 细胞受体 (TCR) 的配体要多样化得多。然而,现在很清楚,γδ TCR 也可以识别 MHC 类样分子,包括 CD1b、CD1c、CD1d 和 MHC 类相关蛋白 1 (MR1)。然而,我们对 γδ T 细胞对 CD1 和 MR1 的免疫的分子水平的理解仍然非常有限。在这里,我们讨论了支持 γδ TCR 识别抗原、抗原呈递分子或两者的新分子范例。最近发现 γδ TCR 在抗原呈递平台下方的位置识别 MR1,这一发现强化了这样一种观点,即 γδ TCR 可以从许多方向接近它们的配体,而不像 αβ TCR 那样以对齐的、端到端的方式结合 MHC、CD1 和 MR1 靶标。

相似文献

1
CD1 and MR1 recognition by human γδ T cells.
Mol Immunol. 2021 May;133:95-100. doi: 10.1016/j.molimm.2020.12.008. Epub 2021 Feb 23.
2
Recognition of the antigen-presenting molecule MR1 by a Vδ3 γδ T cell receptor.
Proc Natl Acad Sci U S A. 2021 Dec 7;118(49). doi: 10.1073/pnas.2110288118.
3
A class of γδ T cell receptors recognize the underside of the antigen-presenting molecule MR1.
Science. 2019 Dec 20;366(6472):1522-1527. doi: 10.1126/science.aav3900.
4
The T cell antigen receptor: the Swiss army knife of the immune system.
Clin Exp Immunol. 2015 Jul;181(1):1-18. doi: 10.1111/cei.12622. Epub 2015 May 14.
5
Lipid and small-molecule display by CD1 and MR1.
Nat Rev Immunol. 2015 Oct;15(10):643-54. doi: 10.1038/nri3889. Epub 2015 Sep 21.
6
Modeling T cell receptor recognition of CD1-lipid and MR1-metabolite complexes.
BMC Bioinformatics. 2014 Sep 26;15(1):319. doi: 10.1186/1471-2105-15-319.
7
Human T cells use CD1 and MR1 to recognize lipids and small molecules.
Curr Opin Chem Biol. 2014 Dec;23:31-8. doi: 10.1016/j.cbpa.2014.09.007. Epub 2014 Sep 29.
8
γδ TCR Recognition of MR1: Adapting to Life on the Flip Side.
Trends Biochem Sci. 2020 Jul;45(7):551-553. doi: 10.1016/j.tibs.2020.03.012. Epub 2020 Apr 13.
9
Diverse antigen presentation by the Group 1 CD1 molecule, CD1c.
Mol Immunol. 2013 Sep;55(2):182-5. doi: 10.1016/j.molimm.2012.10.019. Epub 2012 Nov 3.
10
Editorial: Role of CD1- and MR1-Restricted T Cells in Immunity and Disease.
Front Immunol. 2019 Aug 6;10:1837. doi: 10.3389/fimmu.2019.01837. eCollection 2019.

引用本文的文献

2
Recognition of MR1-antigen complexes by TCR Vγ9Vδ2.
Front Immunol. 2025 Feb 18;16:1519128. doi: 10.3389/fimmu.2025.1519128. eCollection 2025.
3
Research Progress of γδT Cells in Tumor Immunotherapy.
Cancer Control. 2024 Jan-Dec;31:10732748241284863. doi: 10.1177/10732748241284863.
4
Current annotation strategies for T cell phenotyping of single-cell RNA-seq data.
Front Immunol. 2023 Dec 21;14:1306169. doi: 10.3389/fimmu.2023.1306169. eCollection 2023.
5
Strategies to improve γδTCRs engineered T-cell therapies for the treatment of solid malignancies.
Front Immunol. 2023 Jun 27;14:1159337. doi: 10.3389/fimmu.2023.1159337. eCollection 2023.

本文引用的文献

1
Human γδ T cells recognize CD1b by two distinct mechanisms.
Proc Natl Acad Sci U S A. 2020 Sep 15;117(37):22944-22952. doi: 10.1073/pnas.2010545117. Epub 2020 Aug 31.
3
Ligand-dependent downregulation of MR1 cell surface expression.
Proc Natl Acad Sci U S A. 2020 May 12;117(19):10465-10475. doi: 10.1073/pnas.2003136117. Epub 2020 Apr 27.
4
Butyrophilin 2A1 is essential for phosphoantigen reactivity by γδ T cells.
Science. 2020 Feb 7;367(6478). doi: 10.1126/science.aay5516. Epub 2020 Jan 9.
5
A class of γδ T cell receptors recognize the underside of the antigen-presenting molecule MR1.
Science. 2019 Dec 20;366(6472):1522-1527. doi: 10.1126/science.aav3900.
7
Distinct CD1d docking strategies exhibited by diverse Type II NKT cell receptors.
Nat Commun. 2019 Nov 20;10(1):5242. doi: 10.1038/s41467-019-12941-9.
8
Butyrophilin-like 3 Directly Binds a Human Vγ4 T Cell Receptor Using a Modality Distinct from Clonally-Restricted Antigen.
Immunity. 2019 Nov 19;51(5):813-825.e4. doi: 10.1016/j.immuni.2019.09.006. Epub 2019 Oct 15.
9
γδ TCR ligands: the quest to solve a 500-million-year-old mystery.
Nat Immunol. 2019 Feb;20(2):121-128. doi: 10.1038/s41590-018-0304-y. Epub 2019 Jan 21.
10
Recasting Human Vδ1 Lymphocytes in an Adaptive Role.
Trends Immunol. 2018 Jun;39(6):446-459. doi: 10.1016/j.it.2018.03.003. Epub 2018 Apr 18.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验