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The ongoing saga of the mechanism(s) of MHC class I-restricted cross-presentation.MHC I类限制性交叉呈递机制的持续研究历程。
Curr Opin Immunol. 2017 Jun;46:89-96. doi: 10.1016/j.coi.2017.03.015. Epub 2017 May 18.
2
Invariant chain as a vehicle to load antigenic peptides on human MHC class I for cytotoxic T-cell activation.不变链作为一种载体,将抗原肽加载到人 MHC Ⅰ类分子上,用于细胞毒性 T 细胞的激活。
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3
MHC class I assembly: out and about.MHC I类分子组装:走出内质网并四处游走
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Antigen storage compartments in mature dendritic cells facilitate prolonged cytotoxic T lymphocyte cross-priming capacity.成熟树突状细胞中的抗原储存区室有助于延长细胞毒性T淋巴细胞的交叉呈递能力。
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Bacterial heat shock proteins promote CD91-dependent class I MHC cross-presentation of chaperoned peptide to CD8+ T cells by cytosolic mechanisms in dendritic cells versus vacuolar mechanisms in macrophages.细菌热休克蛋白通过树突状细胞中的胞质机制与巨噬细胞中的液泡机制,促进伴侣肽的CD91依赖性I类主要组织相容性复合体交叉呈递给CD8 + T细胞。
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6
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Intracellular delivery of a cytolytic T-lymphocyte epitope peptide by pertussis toxin to major histocompatibility complex class I without involvement of the cytosolic class I antigen processing pathway.百日咳毒素将溶细胞性T淋巴细胞表位肽递送至主要组织相容性复合体I类分子的细胞内过程,且不涉及胞质I类抗原加工途径。
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Presentation of exogenous protein antigens on major histocompatibility complex class I molecules by dendritic cells: pathway of presentation and regulation by cytokines.树突状细胞在主要组织相容性复合体I类分子上呈递外源性蛋白质抗原:呈递途径及细胞因子的调节
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Alternative processing pathways for MHC class I-restricted epitope presentation to CD8+ cytotoxic T lymphocytes.MHC I类限制性表位呈递给CD8+细胞毒性T淋巴细胞的替代加工途径。
Biol Chem Hoppe Seyler. 1994 Nov;375(11):731-6. doi: 10.1515/bchm3.1994.375.11.731.
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Cross-presentation: underlying mechanisms and role in immune surveillance.交叉呈递:潜在机制及其在免疫监视中的作用
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本文引用的文献

1
RAB43 facilitates cross-presentation of cell-associated antigens by CD8α+ dendritic cells.RAB43促进CD8α+树突状细胞对细胞相关抗原的交叉呈递。
J Exp Med. 2016 Dec 12;213(13):2871-2883. doi: 10.1084/jem.20160597. Epub 2016 Nov 29.
2
Rab22a controls MHC-I intracellular trafficking and antigen cross-presentation by dendritic cells.Rab22a控制主要组织相容性复合体I类分子(MHC-I)在细胞内的运输以及树突状细胞的抗原交叉呈递。
EMBO Rep. 2016 Dec;17(12):1753-1765. doi: 10.15252/embr.201642358. Epub 2016 Oct 10.
3
TAP-Dependent and -Independent Peptide Import into Dendritic Cell Phagosomes.依赖TAP及不依赖TAP的肽段导入树突状细胞吞噬体
J Immunol. 2016 Nov 1;197(9):3454-3463. doi: 10.4049/jimmunol.1501925. Epub 2016 Sep 23.
4
Organization of the native ribosome-translocon complex at the mammalian endoplasmic reticulum membrane.哺乳动物内质网膜上天然核糖体-转位子复合物的组织形式。
Biochim Biophys Acta. 2016 Oct;1860(10):2122-9. doi: 10.1016/j.bbagen.2016.06.024. Epub 2016 Jun 29.
5
Dendritic cell maturation and cross-presentation: timing matters!树突状细胞成熟与交叉呈递:时机至关重要!
Immunol Rev. 2016 Jul;272(1):97-108. doi: 10.1111/imr.12432.
6
Lipid peroxidation causes endosomal antigen release for cross-presentation.脂质过氧化导致内体抗原释放以进行交叉呈递。
Sci Rep. 2016 Feb 24;6:22064. doi: 10.1038/srep22064.
7
Interaction of TAPBPR, a tapasin homolog, with MHC-I molecules promotes peptide editing.TAPBPR(一种与塔帕辛同源的蛋白)与主要组织相容性复合体I类(MHC-I)分子的相互作用促进肽段编辑。
Proc Natl Acad Sci U S A. 2016 Feb 23;113(8):E1006-15. doi: 10.1073/pnas.1519894113. Epub 2016 Feb 11.
8
Toll-like Receptor 4 Engagement on Dendritic Cells Restrains Phago-Lysosome Fusion and Promotes Cross-Presentation of Antigens.树突状细胞上 Toll 样受体 4 的交联抑制吞噬溶酶体融合并促进抗原的交叉呈递。
Immunity. 2015 Dec 15;43(6):1087-100. doi: 10.1016/j.immuni.2015.11.006.
9
TAPBPR alters MHC class I peptide presentation by functioning as a peptide exchange catalyst.TAPBPR通过作为肽交换催化剂发挥作用,改变MHC I类肽的呈递。
Elife. 2015 Oct 6;4:e09617. doi: 10.7554/eLife.09617.
10
Cross-Presentation of Cell-Associated Antigens by MHC Class I in Dendritic Cell Subsets.树突状细胞亚群中MHC I类分子对细胞相关抗原的交叉呈递
Front Immunol. 2015 Jul 17;6:363. doi: 10.3389/fimmu.2015.00363. eCollection 2015.

MHC I类限制性交叉呈递机制的持续研究历程。

The ongoing saga of the mechanism(s) of MHC class I-restricted cross-presentation.

作者信息

Grotzke Jeff E, Sengupta Debrup, Lu Qiao, Cresswell Peter

机构信息

Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520-8011, United States.

Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520-8011, United States; Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06520-8011, United States.

出版信息

Curr Opin Immunol. 2017 Jun;46:89-96. doi: 10.1016/j.coi.2017.03.015. Epub 2017 May 18.

DOI:10.1016/j.coi.2017.03.015
PMID:28528219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5554740/
Abstract

Cross-presentation is an MHC-I antigen processing pathway that results in the presentation of peptides from exogenous viral, bacterial, parasitic, and tumor antigens and ultimately leads to priming of naïve CD8 T cells. This process involves several cellular compartments and multiple components. Successful generation of MHC-I-peptide complexes requires that these components act together in a coordinated fashion. We discuss recent findings on the source of MHC-I, the role of the TAP transporter, the importance of intracellular trafficking events, mechanisms of antigen access the cytosol, and how innate immune signals can affect presentation, with an emphasis on how these pathways compare to conventional antigen presentation and how they correlate with existing data.

摘要

交叉呈递是一种MHC-I抗原加工途径,可导致外源性病毒、细菌、寄生虫和肿瘤抗原的肽段呈递,并最终引发初始CD8 T细胞的激活。这一过程涉及多个细胞区室和多种成分。成功生成MHC-I-肽复合物需要这些成分以协调的方式共同发挥作用。我们讨论了关于MHC-I来源、TAP转运体的作用、细胞内运输事件的重要性、抗原进入胞质溶胶的机制以及固有免疫信号如何影响呈递的最新研究结果,重点关注这些途径与传统抗原呈递的比较以及它们与现有数据的相关性。