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免疫抑制多发性硬化症患者从 SARS-CoV-2 感染中康复后的免疫特征。

Immunologic characterization of a immunosuppressed multiple sclerosis patient that recovered from SARS-CoV-2 infection.

机构信息

Flow Cytometry Laboratory, Diagnostic Department, ASST Spedali Civili di Brescia, Brescia, Italy.

Centro di Ricerca Emato-oncologica AIL (CREA), Diagnostic Department, ASST Spedali Civili di Brescia, Brescia, Italy.

出版信息

J Neuroimmunol. 2020 Aug 15;345:577282. doi: 10.1016/j.jneuroim.2020.577282. Epub 2020 May 29.

DOI:10.1016/j.jneuroim.2020.577282
PMID:32505908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7256606/
Abstract

A multiple sclerosis patient infected by SARS-CoV-2 during fingolimod therapy was hospitalized with moderate clinical features, and recovered in 15 days. High levels of CCL5 and CCL10 chemokines and of antibody-secreting B cells were detected, while the levels other B- and T-cell subsets were comparable to that of appropriate controls. However, CD4+ and CD8+ cells were oligoclonally expanded and prone to apoptosis when stimulated in vitro. This study suggests that fingolimod-immunosuppressed patients, despite the low circulating lymphocytes, may rapidly expand antibody-secreting cells and mount an effective immune response that favors COVID-19 recovery after drug discontinuation.

摘要

一名多发性硬化症患者在接受芬戈莫德治疗期间感染了 SARS-CoV-2,出现中等临床特征,15 天后康复。研究人员检测到高水平的趋化因子 CCL5 和 CCL10 以及分泌抗体的 B 细胞,而其他 B 细胞和 T 细胞亚群的水平与适当的对照相当。然而,体外刺激时,CD4+和 CD8+细胞呈寡克隆扩增且易发生凋亡。这项研究表明,尽管芬戈莫德抑制免疫的患者循环淋巴细胞数量较低,但他们可能会迅速扩增分泌抗体的细胞,并产生有效的免疫反应,有利于停药后 COVID-19 的康复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d243/7256606/13e1602726fa/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d243/7256606/463c8107f3ca/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d243/7256606/13e1602726fa/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d243/7256606/463c8107f3ca/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d243/7256606/13e1602726fa/gr1_lrg.jpg

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