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本文引用的文献

1
CD1b-restricted GEM T cell responses are modulated by mycolic acid meromycolate chains.CD1b 限制性 GEM T 细胞反应受类脂阿拉伯甘露糖脂的酰基链调节。
Proc Natl Acad Sci U S A. 2017 Dec 19;114(51):E10956-E10964. doi: 10.1073/pnas.1708252114. Epub 2017 Nov 20.
2
A molecular basis of human T cell receptor autoreactivity toward self-phospholipids.人类 T 细胞受体对自身磷脂的自身反应性的分子基础。
Sci Immunol. 2017 Oct 20;2(16). doi: 10.1126/sciimmunol.aao1384.
3
Four pathways of CD1 antigen presentation to T cells.CD1抗原提呈给T细胞的四条途径。
Curr Opin Immunol. 2017 Jun;46:127-133. doi: 10.1016/j.coi.2017.07.013. Epub 2017 Jul 28.
4
CD1b-mycolic acid tetramers demonstrate T-cell fine specificity for mycobacterial lipid tails.CD1b-分枝菌酸四聚体显示出对分枝杆菌脂质尾部的T细胞精细特异性。
Eur J Immunol. 2017 Sep;47(9):1525-1534. doi: 10.1002/eji.201747062. Epub 2017 Jul 31.
5
Functionally diverse human T cells recognize non-microbial antigens presented by MR1.功能多样的人类T细胞识别由MR1呈递的非微生物抗原。
Elife. 2017 May 18;6:e24476. doi: 10.7554/eLife.24476.
6
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Chemistry. 2017 Jan 31;23(7):1694-1701. doi: 10.1002/chem.201605287. Epub 2017 Jan 18.
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CD1b-autoreactive T cells recognize phospholipid antigens and contribute to antitumor immunity against a CD1b T cell lymphoma.CD1b自身反应性T细胞识别磷脂抗原,并有助于对抗CD1b T细胞淋巴瘤的抗肿瘤免疫。
Oncoimmunology. 2016 Jul 22;5(9):e1213932. doi: 10.1080/2162402X.2016.1213932. eCollection 2016.
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Psoriatic T cells recognize neolipid antigens generated by mast cell phospholipase delivered by exosomes and presented by CD1a.银屑病T细胞识别由肥大细胞磷脂酶产生、通过外泌体传递并由CD1a呈递的新脂质抗原。
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CD1 脂质抗原呈递途径的多功能性。

The versatility of the CD1 lipid antigen presentation pathway.

机构信息

Faculty of Medicine, Academic Unit of Clinical and Experimental Sciences, Southampton, UK.

F.Hoffmann-La Roche Ltd, Basel, Switzerland.

出版信息

Immunology. 2018 Jun;154(2):196-203. doi: 10.1111/imm.12912. Epub 2018 Mar 24.

DOI:10.1111/imm.12912
PMID:29460282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5980215/
Abstract

The family of non-classical major histocompatibility complex (MHC) class-I like CD1 molecules has an emerging role in human disease. Group 1 CD1 includes CD1a, CD1b and CD1c, which function to display lipids on the cell surface of antigen-presenting cells for direct recognition by T-cells. The recent advent of CD1 tetramers and the identification of novel lipid ligands has contributed towards the increasing number of CD1-restricted T-cell clones captured. These advances have helped to identify novel donor unrestricted and semi-invariant T-cell populations in humans and new mechanisms of T-cell recognition. However, although there is an opportunity to design broadly acting lipids and harness the therapeutic potential of conserved T-cells, knowledge of their role in health and disease is lacking. We briefly summarize the current evidence implicating group 1 CD1 molecules in infection, cancer and autoimmunity and show that although CD1 are not as diverse as MHC, recent discoveries highlight their versatility as they exhibit intricate mechanisms of antigen presentation.

摘要

非经典主要组织相容性复合体(MHC)I 类样 CD1 分子家族在人类疾病中具有新兴作用。第 1 组 CD1 包括 CD1a、CD1b 和 CD1c,它们的功能是在抗原呈递细胞的细胞表面展示脂质,以便 T 细胞直接识别。最近出现的 CD1 四聚体和新的脂质配体的鉴定,有助于捕获越来越多的 CD1 限制性 T 细胞克隆。这些进展有助于在人类中鉴定新型非供体受限和半不变 T 细胞群体,以及 T 细胞识别的新机制。然而,尽管有机会设计广泛作用的脂质并利用保守 T 细胞的治疗潜力,但对它们在健康和疾病中的作用知之甚少。我们简要总结了目前与第 1 组 CD1 分子在感染、癌症和自身免疫中的关联的证据,并表明,尽管 CD1 不如 MHC 多样化,但最近的发现强调了它们的多功能性,因为它们表现出复杂的抗原呈递机制。