当前位置:科学网首页 > 小柯机器人 >详情
COVID-19康复患者中存在强烈的CD4+和CD8+记忆T细胞
作者:小柯机器人 发布时间:2020/9/9 17:12:53

英国牛津大学Tao Dong研究团队发现,COVID-19康复患者中存在SARS-CoV-2引发的强烈CD4+和CD8+记忆T细胞。这一研究成果于2020年9月4日在线发表在《自然—免疫学》上。

通过使用基于干扰素γ的测定方法来检测SARS-CoV-2中除了ORF1以外的肽段,研究人员揭示了42名从COVID-19中恢复后的患者(28名轻症和14名重症)以及16名未感染者的T细胞记忆。与轻症病例相比,重症T细胞应答的广度和强度明显更高。总体的和突刺蛋白特异性的T细胞应答与突刺蛋白特异性抗体应答相关。
 
研究人员鉴定出41个含有CD4+和/或CD8+表位的肽,包括六个免疫主导区域。六个优化的CD8+表位被定义,其中肽-MHC五聚体-阳性细胞表现出中央型和效应型记忆表型。在轻症病例中,更高比例的SARS-CoV-2特异性CD8+T细胞被观察到。与轻症疾病相关T细胞应答的鉴定将促进对保护性免疫的理解,并强调了在未来的COVID-19疫苗设计中应关注非突刺蛋白。
 
据悉,SARS-CoV-2疫苗和治疗剂的开发将取决于对病毒免疫力的了解。
 
附:英文原文

Title: Broad and strong memory CD4 + and CD8 + T cells induced by SARS-CoV-2 in UK convalescent individuals following COVID-19

Author: Yanchun Peng, Alexander J. Mentzer, Guihai Liu, Xuan Yao, Zixi Yin, Danning Dong, Wanwisa Dejnirattisai, Timothy Rostron, Piyada Supasa, Chang Liu, Csar Lpez-Camacho, Jose Slon-Campos, Yuguang Zhao, David I. Stuart, Guido C. Paesen, Jonathan M. Grimes, Alfred A. Antson, Oliver W. Bayfield, Dorothy E. D. P. Hawkins, De-Sheng Ker, Beibei Wang, Lance Turtle, Krishanthi Subramaniam, Paul Thomson, Ping Zhang, Christina Dold, Jeremy Ratcliff, Peter Simmonds, Thushan de Silva, Paul Sopp, Dannielle Wellington, Ushani Rajapaksa, Yi-Ling Chen, Mariolina Salio, Giorgio Napolitani, Wayne Paes, Persephone Borrow, Benedikt M. Kessler, Jeremy W. Fry, Nikolai F. Schwabe, Malcolm G. Semple, J. Kenneth Baillie, Shona C. Moore, Peter J. M. Openshaw, M. Azim Ansari, Susanna Dunachie, Eleanor Barnes, John Frater, Georgina Kerr, Philip Goulder, Teresa Lockett, Robert Levin, Yonghong Zhang, Ronghua Jing, Ling-Pei Ho, Richard J. Cornall, Christopher P. Conlon

Issue&Volume: 2020-09-04

Abstract: The development of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines and therapeutics will depend on understanding viral immunity. We studied T cell memory in 42 patients following recovery from COVID-19 (28 with mild disease and 14 with severe disease) and 16 unexposed donors, using interferon-γ-based assays with peptides spanning SARS-CoV-2 except ORF1. The breadth and magnitude of T cell responses were significantly higher in severe as compared with mild cases. Total and spike-specific T cell responses correlated with spike-specific antibody responses. We identified 41 peptides containing CD4+ and/or CD8+ epitopes, including six immunodominant regions. Six optimized CD8+ epitopes were defined, with peptide–MHC pentamer-positive cells displaying the central and effector memory phenotype. In mild cases, higher proportions of SARS-CoV-2-specific CD8+ T cells were observed. The identification of T cell responses associated with milder disease will support an understanding of protective immunity and highlights the potential of including non-spike proteins within future COVID-19 vaccine design.

DOI: 10.1038/s41590-020-0782-6

Source: https://www.nature.com/articles/s41590-020-0782-6

期刊信息

Nature Immunology:《自然—免疫学》,创刊于2000年。隶属于施普林格·自然出版集团,最新IF:23.53
官方网址:https://www.nature.com/ni/
投稿链接:https://mts-ni.nature.com/cgi-bin/main.plex