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多因素血清学分析揭示了既往人类冠状病毒反应对 SARS-CoV-2 免疫的贡献。

Multifactorial seroprofiling dissects the contribution of pre-existing human coronaviruses responses to SARS-CoV-2 immunity.

机构信息

Institute of Medical Virology, University of Zurich, Zurich, Switzerland.

Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, Zurich, Switzerland.

出版信息

Nat Commun. 2021 Nov 18;12(1):6703. doi: 10.1038/s41467-021-27040-x.

DOI:10.1038/s41467-021-27040-x
PMID:34795285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8602384/
Abstract

Determination of SARS-CoV-2 antibody responses in the context of pre-existing immunity to circulating human coronavirus (HCoV) is critical for understanding protective immunity. Here we perform a multifactorial analysis of SARS-CoV-2 and HCoV antibody responses in pre-pandemic (N = 825) and SARS-CoV-2-infected donors (N = 389) using a custom-designed multiplex ABCORA assay. ABCORA seroprofiling, when combined with computational modeling, enables accurate definition of SARS-CoV-2 seroconversion and prediction of neutralization activity, and reveals intriguing interrelations with HCoV immunity. Specifically, higher HCoV antibody levels in SARS-CoV-2-negative donors suggest that pre-existing HCoV immunity may provide protection against SARS-CoV-2 acquisition. In those infected, higher HCoV activity is associated with elevated SARS-CoV-2 responses, indicating cross-stimulation. Most importantly, HCoV immunity may impact disease severity, as patients with high HCoV reactivity are less likely to require hospitalization. Collectively, our results suggest that HCoV immunity may promote rapid development of SARS-CoV-2-specific immunity, thereby underscoring the importance of exploring cross-protective responses for comprehensive coronavirus prevention.

摘要

在了解保护性免疫的过程中,确定 SARS-CoV-2 抗体反应与循环人类冠状病毒(HCoV)的预先存在的免疫之间的关系至关重要。在这里,我们使用定制的多路复用 ABCORA 测定法,对大流行前(N=825)和 SARS-CoV-2 感染供体(N=389)中的 SARS-CoV-2 和 HCoV 抗体反应进行了多因素分析。ABCORA 血清分析与计算模型相结合,可以准确定义 SARS-CoV-2 血清转化并预测中和活性,并揭示了与 HCoV 免疫的有趣关系。具体而言,SARS-CoV-2 阴性供体中较高的 HCoV 抗体水平表明,预先存在的 HCoV 免疫可能提供针对 SARS-CoV-2 获得的保护。在感染者中,较高的 HCoV 活性与 SARS-CoV-2 反应的升高相关,表明交叉刺激。最重要的是,HCoV 免疫可能会影响疾病的严重程度,因为具有高 HCoV 反应性的患者不太可能需要住院治疗。总之,我们的结果表明,HCoV 免疫可能会促进 SARS-CoV-2 特异性免疫的快速发展,从而强调了探索交叉保护反应以进行全面冠状病毒预防的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/2e12a020388a/41467_2021_27040_Fig8_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/50ebaec5578a/41467_2021_27040_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/54b20b1e641f/41467_2021_27040_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/68d8a12f4b66/41467_2021_27040_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/d42652dee9b0/41467_2021_27040_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/2e12a020388a/41467_2021_27040_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/b2f585ee09b0/41467_2021_27040_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/30f44c4329c0/41467_2021_27040_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/dfe3e3371d48/41467_2021_27040_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/50ebaec5578a/41467_2021_27040_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/54b20b1e641f/41467_2021_27040_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/68d8a12f4b66/41467_2021_27040_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/d42652dee9b0/41467_2021_27040_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20b3/8602384/2e12a020388a/41467_2021_27040_Fig8_HTML.jpg

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