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预先存在的与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)发生交叉反应的体液免疫可能预防危重症患者因冠状病毒病2019(COVID-19)死亡。

Preexisting Humoral Immunity Cross-Reacting with SARS-CoV-2 Might Prevent Death Due to COVID-19 in Critical Patients.

作者信息

Yamashita Taro, Shimakami Tetsuro, Nio Kouki, Terashima Takeshi, Okajima Masaki, Taniguchi Takumi, Wada Takashi, Honda Masao, Gabata Toshifumi, Ota Kenji, Yanagihara Katsunori, Kaneko Shuichi

机构信息

Department of General Medicine, Kanazawa University Hospital, Kanazawa 920-8641, Japan.

Center for Education in Community Medicine, Kanazawa University Hospital, Kanazawa 920-8641, Japan.

出版信息

J Clin Med. 2022 Jul 4;11(13):3870. doi: 10.3390/jcm11133870.

DOI:10.3390/jcm11133870
PMID:35807155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9267280/
Abstract

The preexistence of humoral immunity, which cross-reacts with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) protein due to prior endemic low-pathogenic human coronavirus infection, has been reported, but its role in coronavirus disease 2019 (COVID-19) outcomes remains elusive. We evaluated serum samples obtained from 368 patients before the pandemic and 1423 independent serum samples from patients during the pandemic. We found that approximately 6~13% and 1.5% of patients had IgG cross-reactivity to the SARS-CoV-2 spike and nucleocapsid proteins in both cohorts. We evaluated the IgG cross-reactivity to the SARS-CoV-2 spike and nucleocapsid proteins in 48 severe or critical COVID-19 patients to evaluate if the elevation of IgG was evoked as a primary response (IgG elevation from 10 days after antigen exposure) or boosted as a secondary response (IgG elevation immediately after antigen exposure). Approximately 50% of patients showed humoral immune responses to the nucleocapsid protein of SARS-CoV-2. Importantly, none of the critically ill patients with this humoral immunity died, whereas 40% of patients without this immunity did. Taken together, subjects had humoral immunity to SARS-CoV-2 nucleocapsid but not spike before the pandemic, which might prevent critically ill COVID-19 patients from dying.

摘要

据报道,由于既往地方性低致病性人冠状病毒感染,存在与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)蛋白发生交叉反应的体液免疫,但它在2019冠状病毒病(COVID-19)结局中的作用仍不明确。我们评估了大流行前从368例患者获得的血清样本以及大流行期间从患者获得的1423份独立血清样本。我们发现,在两个队列中,分别约有6%~13%和1.5%的患者对SARS-CoV-2刺突蛋白和核衣壳蛋白具有IgG交叉反应性。我们评估了48例重症或危重症COVID-19患者对SARS-CoV-2刺突蛋白和核衣壳蛋白的IgG交叉反应性,以评估IgG升高是作为主要反应(抗原暴露10天后IgG升高)诱发的,还是作为次要反应(抗原暴露后立即IgG升高)增强的。约50%的患者对SARS-CoV-2核衣壳蛋白表现出体液免疫反应。重要的是,具有这种体液免疫的危重症患者无一死亡,而没有这种免疫的患者中有40%死亡。综上所述,在大流行前,受试者对SARS-CoV-2核衣壳具有体液免疫,但对刺突蛋白没有,这可能会防止重症COVID-19患者死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/0f1cbecf0b23/jcm-11-03870-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/8a3b7ff038d2/jcm-11-03870-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/3a6a5f91aa54/jcm-11-03870-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/8457882a1c5d/jcm-11-03870-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/5508e8dccab0/jcm-11-03870-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/c1036df63486/jcm-11-03870-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/0f1cbecf0b23/jcm-11-03870-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/8a3b7ff038d2/jcm-11-03870-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/3a6a5f91aa54/jcm-11-03870-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/8457882a1c5d/jcm-11-03870-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/5508e8dccab0/jcm-11-03870-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/c1036df63486/jcm-11-03870-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/623b/9267280/0f1cbecf0b23/jcm-11-03870-g006.jpg

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