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Sci Rep. 2021 Mar 11;11(1):5803. doi: 10.1038/s41598-021-85081-0.
2
Multi-clonal SARS-CoV-2 neutralization by antibodies isolated from severe COVID-19 convalescent donors.从重症 COVID-19 康复者供体中分离出的抗体对 SARS-CoV-2 的多克隆中和作用。
PLoS Pathog. 2021 Feb 11;17(2):e1009165. doi: 10.1371/journal.ppat.1009165. eCollection 2021 Feb.
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mRNA vaccine-elicited antibodies to SARS-CoV-2 and circulating variants.mRNA 疫苗诱导的针对 SARS-CoV-2 和循环变异株的抗体。
Nature. 2021 Apr;592(7855):616-622. doi: 10.1038/s41586-021-03324-6. Epub 2021 Feb 10.
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Clinical progression and outcomes of 260 patients with severe COVID-19: an observational study.260 例重症 COVID-19 患者的临床进展和结局:一项观察性研究。
Sci Rep. 2021 Feb 4;11(1):3166. doi: 10.1038/s41598-021-82943-5.
5
Human antibodies targeting a Mycobacterium transporter protein mediate protection against tuberculosis.靶向分枝杆菌转运蛋白的人源抗体可介导对结核病的保护。
Nat Commun. 2021 Jan 27;12(1):602. doi: 10.1038/s41467-021-20930-0.
6
Preexisting immunity shapes distinct antibody landscapes after influenza virus infection and vaccination in humans.既往免疫在人类感染流感病毒和接种疫苗后塑造了不同的抗体格局。
Sci Transl Med. 2020 Dec 9;12(573). doi: 10.1126/scitranslmed.abd3601.
7
SARS-CoV-2 Antibody Responses Are Correlated to Disease Severity in COVID-19 Convalescent Individuals.SARS-CoV-2 抗体反应与 COVID-19 恢复期个体的疾病严重程度相关。
J Immunol. 2021 Jan 1;206(1):109-117. doi: 10.4049/jimmunol.2000898. Epub 2020 Nov 18.
8
Serum-IgG responses to SARS-CoV-2 after mild and severe COVID-19 infection and analysis of IgG non-responders.血清 IgG 对轻度和重度 COVID-19 感染后 SARS-CoV-2 的反应以及 IgG 无应答者的分析。
PLoS One. 2020 Oct 21;15(10):e0241104. doi: 10.1371/journal.pone.0241104. eCollection 2020.
9
Occurrence and transmission potential of asymptomatic and presymptomatic SARS-CoV-2 infections: A living systematic review and meta-analysis.无症状和出现症状前 SARS-CoV-2 感染的发生和传播潜力:一项实时系统评价和荟萃分析。
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10
Neutralizing nanobodies bind SARS-CoV-2 spike RBD and block interaction with ACE2.中和纳米抗体结合 SARS-CoV-2 刺突 RBD 并阻断与 ACE2 的相互作用。
Nat Struct Mol Biol. 2020 Sep;27(9):846-854. doi: 10.1038/s41594-020-0469-6. Epub 2020 Jul 13.

抗体:让我们更强大的原因。

Antibodies: what makes us stronger.

机构信息

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Hum Vaccin Immunother. 2021 Oct 3;17(10):3551-3553. doi: 10.1080/21645515.2021.1929034. Epub 2021 May 25.

DOI:10.1080/21645515.2021.1929034
PMID:34032550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8437519/
Abstract

Neutralizing antibodies are the basis of almost all approved prophylactic vaccines and the foundation of effective protection from pathogens, including the recently emerging SARS Coronavirus 2 (SARS-CoV-2). However, the contribution of antibodies to protection and to the course of the disease during first-time exposure to a pathogen is unknown. We analyzed the antibodies and B cell responses in severe and mild COVID-19 patients. Despite our primary assumption that high antibody titers contribute to a mild disease, we found that severe COVID-19 illness, and not mild infection, correlates with strong anti-viral antibody and memory B cell responses. This phenomenon was also demonstrated for anti-Mycobacterium inhibiting antibodies that we recently isolated from an actively infected Tuberculosis-sick donor. This correlation between disease severity and antibody responses can be explained by the fact that high viral loads drive B cell stimulation and generation of high-affinity antibodies that will be protective upon future encounter with the particular pathogen.

摘要

中和抗体几乎是所有获批预防性疫苗的基础,也是针对病原体(包括最近出现的 SARS 冠状病毒 2(SARS-CoV-2))产生有效保护的基础。然而,抗体在初次接触病原体时对保护和疾病进程的贡献尚不清楚。我们分析了重症和轻症 COVID-19 患者的抗体和 B 细胞反应。尽管我们最初的假设是高抗体滴度有助于疾病的轻症化,但我们发现严重的 COVID-19 疾病,而不是轻症感染,与强烈的抗病毒抗体和记忆 B 细胞反应相关。我们最近从一名活动性感染结核病的捐赠者中分离出的抗分枝杆菌抑制抗体也证明了这一现象。这种疾病严重程度与抗体反应之间的相关性可以用以下事实来解释:高病毒载量会驱动 B 细胞的刺激和高亲和力抗体的产生,这些抗体在未来遇到特定病原体时将具有保护作用。