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COVID-19 恢复期个体中的 Spike 特异性循环滤泡辅助 T 细胞和交叉中和抗体反应。

Spike-specific circulating T follicular helper cell and cross-neutralizing antibody responses in COVID-19-convalescent individuals.

机构信息

Translational Medicine Institute, The First People's Hospital of Chenzhou, University of South China, Chenzhou, China.

The Central Hospital of Shaoyang, Shaoyang, China.

出版信息

Nat Microbiol. 2021 Jan;6(1):51-58. doi: 10.1038/s41564-020-00824-5. Epub 2020 Nov 16.

Abstract

Coronavirus disease 2019 (COVID-19) is caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and individuals with COVID-19 have symptoms that can be asymptomatic, mild, moderate or severe. In the early phase of infection, T- and B-cell counts are substantially decreased; however, IgM and IgG are detectable within 14 d after symptom onset. In COVID-19-convalescent individuals, spike-specific neutralizing antibodies are variable. No specific drug or vaccine is available for COVID-19 at the time of writing; however, patients benefit from treatment with serum from COVID-19-convalescent individuals. Nevertheless, antibody responses and cross-reactivity with other coronaviruses in COVID-19-convalescent individuals are largely unknown. Here, we show that the majority of COVID-19-convalescent individuals maintained SARS-CoV-2 spike S1- and S2-specific antibodies with neutralizing activity against the SARS-CoV-2 pseudotyped virus, and that some of the antibodies cross-neutralized SARS-CoV, Middle East respiratory syndrome coronavirus or both pseudotyped viruses. Convalescent individuals who experienced severe COVID-19 showed higher neutralizing antibody titres, a faster increase in lymphocyte counts and a higher frequency of CXCR3 T follicular help (T) cells compared with COVID-19-convalescent individuals who experienced non-severe disease. Circulating T cells were spike specific and functional, and the frequencies of CXCR3 T cells were positively associated with neutralizing antibody titres in COVID-19-convalescent individuals. No individuals had detectable autoantibodies. These findings provide insights into neutralizing antibody responses in COVID-19-convalescent individuals and facilitate the treatment and vaccine development for SARS-CoV-2 infection.

摘要

新型冠状病毒病(COVID-19)由严重急性呼吸系统综合征冠状病毒 2 型(SARS-CoV-2)感染引起,COVID-19 患者的症状可以是无症状、轻症、中症或重症。在感染早期,T 细胞和 B 细胞计数显著下降;然而,在症状出现后 14 天内可检测到 IgM 和 IgG。在 COVID-19 康复个体中,刺突特异性中和抗体是可变的。在撰写本文时,尚无针对 COVID-19 的特效药物或疫苗;然而,患者从 COVID-19 康复个体的血清治疗中获益。尽管如此,COVID-19 康复个体的抗体反应和与其他冠状病毒的交叉反应在很大程度上是未知的。在这里,我们表明,大多数 COVID-19 康复个体维持针对 SARS-CoV-2 假型病毒具有中和活性的 SARS-CoV-2 刺突 S1 和 S2 特异性抗体,并且一些抗体交叉中和 SARS-CoV、中东呼吸综合征冠状病毒或两者的假型病毒。与经历非重症 COVID-19 的 COVID-19 康复个体相比,经历重症 COVID-19 的康复个体显示出更高的中和抗体滴度、更快的淋巴细胞计数增加和更高频率的 CXCR3 T 滤泡辅助(T)细胞。循环 T 细胞是刺突特异性和功能性的,并且 COVID-19 康复个体中 CXCR3 T 细胞的频率与中和抗体滴度呈正相关。没有个体检测到可检测的自身抗体。这些发现提供了 COVID-19 康复个体中中和抗体反应的见解,并促进了 SARS-CoV-2 感染的治疗和疫苗开发。

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