• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1016/j.molimm.2020.12.008
PMID:33636434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8075093/
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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2c1/8075093/d880d7c7d60f/nihms-1687695-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2c1/8075093/8e1179ea9fce/nihms-1687695-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2c1/8075093/d880d7c7d60f/nihms-1687695-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2c1/8075093/8e1179ea9fce/nihms-1687695-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2c1/8075093/d880d7c7d60f/nihms-1687695-f0002.jpg

相似文献

1
CD1 and MR1 recognition by human γδ T cells.人 γδ T 细胞对 CD1 和 MR1 的识别。
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.Vδ3 γδ T 细胞受体识别抗原呈递分子 MR1。
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 MR1.一类 γδ T 细胞受体识别呈递分子 MR1 下侧。
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.T细胞抗原受体:免疫系统的瑞士军刀。
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.CD1和MR1介导的脂质和小分子呈递
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.建立 T 细胞受体识别 CD1-脂质和 MR1-代谢物复合物的模型。
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.人类 T 细胞使用 CD1 和 MR1 来识别脂质和小分子。
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.γδ TCR 对 MR1 的识别:适应翻转的生活。
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.Ⅰ 类 CD1 分子 CD1c 的多样抗原呈递。
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.社论:CD1 及 MR1 限制型 T 细胞在免疫与疾病中的作用
Front Immunol. 2019 Aug 6;10:1837. doi: 10.3389/fimmu.2019.01837. eCollection 2019.

引用本文的文献

1
Three-Dimensional Modeling of T Cell Receptor Gamma (TRG)_Delta (TRD)/CD1D Complex Reveals Different Binding Interactions Depending on the TRD CDR3 Length.T细胞受体γ(TRG)-δ(TRD)/CD1D复合物的三维建模揭示了取决于TRD互补决定区3(CDR3)长度的不同结合相互作用。
Antibodies (Basel). 2025 May 29;14(2):46. doi: 10.3390/antib14020046.
2
Recognition of MR1-antigen complexes by TCR Vγ9Vδ2.TCR Vγ9Vδ2对MR1-抗原复合物的识别。
Front Immunol. 2025 Feb 18;16:1519128. doi: 10.3389/fimmu.2025.1519128. eCollection 2025.
3
Research Progress of γδT Cells in Tumor Immunotherapy.

本文引用的文献

1
Human γδ T cells recognize CD1b by two distinct mechanisms.人类 γδ T 细胞通过两种不同的机制识别 CD1b。
Proc Natl Acad Sci U S A. 2020 Sep 15;117(37):22944-22952. doi: 10.1073/pnas.2010545117. Epub 2020 Aug 31.
2
Butyrophilin-like proteins display combinatorial diversity in selecting and maintaining signature intraepithelial γδ T cell compartments.但是丝氨酸蛋白酶抑制剂家族蛋白在选择和维持特征性上皮内 γδ T 细胞隔室方面表现出组合多样性。
Nat Commun. 2020 Jul 28;11(1):3769. doi: 10.1038/s41467-020-17557-y.
3
Ligand-dependent downregulation of MR1 cell surface expression.
γδT 细胞在肿瘤免疫治疗中的研究进展。
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.单细胞 RNA 测序数据中 T 细胞表型的当前注释策略。
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.改善用于治疗实体恶性肿瘤的工程化γδT细胞受体疗法的策略。
Front Immunol. 2023 Jun 27;14:1159337. doi: 10.3389/fimmu.2023.1159337. eCollection 2023.
配体依赖性的 MR1 细胞表面表达下调。
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.Butyrophilin 2A1 对于 γδ T 细胞对磷酸抗原的反应至关重要。
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 MR1.一类 γδ T 细胞受体识别呈递分子 MR1 下侧。
Science. 2019 Dec 20;366(6472):1522-1527. doi: 10.1126/science.aav3900.
6
Differential skewing of donor-unrestricted and γδ T cell repertoires in tuberculosis-infected human lungs.结核感染人类肺部中供体非限制和 γδ T 细胞 repertoire 的差异偏斜。
J Clin Invest. 2020 Jan 2;130(1):214-230. doi: 10.1172/JCI130711.
7
Distinct CD1d docking strategies exhibited by diverse Type II NKT cell receptors.不同的 II 型 NKT 细胞受体表现出独特的 CD1d 对接策略。
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.但钛蛋白样 3 直接结合人 Vγ4 T 细胞受体,使用不同于克隆限制抗原的方式。
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.γδ TCR 配体:解决一个 5 亿年历史之谜的探索。
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.重塑人类 Vδ1 淋巴细胞的适应性作用。
Trends Immunol. 2018 Jun;39(6):446-459. doi: 10.1016/j.it.2018.03.003. Epub 2018 Apr 18.