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Selective and cross-reactive SARS-CoV-2 T cell epitopes in unexposed humans.未暴露于 SARS-CoV-2 人群中的选择性和交叉反应性 T 细胞表位。
Science. 2020 Oct 2;370(6512):89-94. doi: 10.1126/science.abd3871. Epub 2020 Aug 4.
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Proteome-Wide Zika Virus CD4 T Cell Epitope and HLA Restriction Determination.全蛋白质组 Zika 病毒 CD4 T 细胞表位和 HLA 限制的鉴定。
Immunohorizons. 2020 Aug 4;4(8):444-453. doi: 10.4049/immunohorizons.2000068.
3
Computationally Optimized SARS-CoV-2 MHC Class I and II Vaccine Formulations Predicted to Target Human Haplotype Distributions.基于计算优化的 SARS-CoV-2 MHC Ⅰ类和Ⅱ类疫苗配方,预测针对人类单倍型分布。
Cell Syst. 2020 Aug 26;11(2):131-144.e6. doi: 10.1016/j.cels.2020.06.009. Epub 2020 Jul 27.
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MHCflurry 2.0: Improved Pan-Allele Prediction of MHC Class I-Presented Peptides by Incorporating Antigen Processing.MHCflurry 2.0:通过纳入抗原加工提高 MHC I 类呈递肽的泛等位基因预测。
Cell Syst. 2020 Jul 22;11(1):42-48.e7. doi: 10.1016/j.cels.2020.06.010. Epub 2020 Jul 14.
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Phenotype and kinetics of SARS-CoV-2-specific T cells in COVID-19 patients with acute respiratory distress syndrome.急性呼吸窘迫综合征的 COVID-19 患者中 SARS-CoV-2 特异性 T 细胞的表型和动力学。
Sci Immunol. 2020 Jun 26;5(48). doi: 10.1126/sciimmunol.abd2071.
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MAIT Cell Activation and Functions.MAIT 细胞的激活与功能。
Front Immunol. 2020 May 27;11:1014. doi: 10.3389/fimmu.2020.01014. eCollection 2020.
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Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals.COVID-19 疾病患者和未接触者体内针对 SARS-CoV-2 冠状病毒的 T 细胞反应的靶标。
Cell. 2020 Jun 25;181(7):1489-1501.e15. doi: 10.1016/j.cell.2020.05.015. Epub 2020 May 20.
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Benchmarking predictions of MHC class I restricted T cell epitopes in a comprehensively studied model system.在一个经过全面研究的模型系统中对 MHC Ⅰ类限制性 T 细胞表位的预测进行基准测试。
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Glycopeptide epitope facilitates HIV-1 envelope specific humoral immune responses by eliciting T cell help.糖肽表位通过诱导 T 细胞辅助来促进 HIV-1 包膜的特异性体液免疫反应。
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NetMHCpan-4.1 and NetMHCIIpan-4.0: improved predictions of MHC antigen presentation by concurrent motif deconvolution and integration of MS MHC eluted ligand data.NetMHCpan-4.1 和 NetMHCIIpan-4.0:通过同时对基序进行分解以及整合 MS MHC 洗脱配体数据,改进了 MHC 抗原呈递的预测。
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表位预测和鉴定——人类适应性 T 细胞反应。

Epitope prediction and identification- adaptive T cell responses in humans.

机构信息

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA.

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA; Department of Medicine, Division of Infectious Diseases and Global Public Health, University of California, San Diego, La Jolla, CA, 92037, USA.

出版信息

Semin Immunol. 2020 Aug;50:101418. doi: 10.1016/j.smim.2020.101418. Epub 2020 Oct 31.

DOI:10.1016/j.smim.2020.101418
PMID:33131981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7749839/
Abstract

Epitopes, in the context of T cell recognition, are short peptides typically derived by antigen processing, and presented on the cell surface bound to MHC molecules (HLA molecules in humans) for TCR scrutiny. The identification of epitopes is a context-dependent process, with consideration given to, for example, the source pathogen and protein, the host organism, and state of the immune reaction (e.g., following natural infection, vaccination, etc.). In the following review, we consider the various approaches used to define T cell epitopes, including both bioinformatic and experimental approaches, and discuss the concepts of immunodominance and immunoprevalence. We also discuss HLA polymorphism and epitope restriction, and the resulting impact on the identification of, and potential population coverage afforded by, epitopes or epitope-based vaccines. Finally, some examples of the practical application of T cell epitope identification are provided, showing how epitopes have been valuable for deriving novel immunological insights in the context of the immune response to various pathogens and allergens.

摘要

在 T 细胞识别的背景下,表位是通过抗原加工产生的短肽,通常与 MHC 分子(人类中的 HLA 分子)结合并呈现在细胞表面,以供 TCR 检查。表位的识别是一个依赖于上下文的过程,需要考虑例如病原体和蛋白质的来源、宿主生物体以及免疫反应的状态(例如,自然感染后、接种疫苗后等)。在以下综述中,我们考虑了用于定义 T 细胞表位的各种方法,包括生物信息学和实验方法,并讨论了免疫显性和免疫普遍性的概念。我们还讨论了 HLA 多态性和表位限制,以及这对表位或基于表位的疫苗的鉴定和潜在人群覆盖的影响。最后,提供了 T 细胞表位鉴定的一些实际应用示例,展示了表位如何在各种病原体和过敏原免疫反应的背景下为获得新的免疫学见解提供了有价值的信息。