Gussarow Daniel, Bonifacius Agnes, Cossmann Anne, Stankov Metodi V, Mausberg Philip, Tischer-Zimmermann Sabine, Gödecke Nina, Kalinke Ulrich, Behrens Georg M N, Blasczyk Rainer, Eiz-Vesper Britta
Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hanover, Germany.
Department of Rheumatology and Clinical Immunology, Hannover Medical School, Hanover, Germany.
Front Med (Lausanne). 2021 Nov 25;8:770381. doi: 10.3389/fmed.2021.770381. eCollection 2021.
Since its declaration as a pandemic in March 2020, SARS-CoV-2 has infected more than 217 million people worldwide and despite mild disease in the majority of the cases, more than 4.5 million cases of COVID-19-associated death have been reported as of September 2021. The question whether recovery from COVID-19 results in prevention of reinfection can be answered with a "no" since cases of reinfections have been reported. The more important question is whether during SARS-CoV-2 infection, a protective immunity is built and maintained afterwards in a way which protects from possibly severe courses of disease in case of a reinfection. A similar question arises with respect to vaccination: as of September 2021, globally, more than 5.2 billion doses of vaccines have been administered. Therefore, it is of utmost importance to study the cellular and humoral immunity toward SARS-CoV-2 in a longitudinal manner. In this study, reconvalescent COVID-19 patients have been followed up for more than 1 year after SARS-CoV-2 infection to characterize in detail the long-term humoral as well as cellular immunity. Both SARS-CoV-2-specific T cells and antibodies could be detected for a period of more than 1 year after infection, indicating that the immune protection established during initial infection is maintained and might possibly protect from severe disease in case of reinfection or infection with novel emerging variants. Moreover, these data demonstrate the opportunity for immunotherapy of hospitalized COVID-19 patients via adoptive transfer of functional antiviral T cells isolated from reconvalescent individuals.
自2020年3月被宣布为大流行病以来,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)已感染全球超过2.17亿人,尽管大多数病例症状较轻,但截至2021年9月,已报告超过450万例与新冠病毒病(COVID-19)相关的死亡病例。由于已有再次感染病例的报告,因此COVID-19康复后是否能预防再次感染的问题答案是否定的。更重要的问题是,在SARS-CoV-2感染期间,是否会建立并随后维持一种保护性免疫,从而在再次感染时防止可能出现的严重病程。关于疫苗接种也出现了类似问题:截至2021年9月,全球已接种超过52亿剂疫苗。因此,纵向研究针对SARS-CoV-2的细胞免疫和体液免疫至关重要。在本研究中,对COVID-19康复患者在SARS-CoV-2感染后进行了1年多的随访,以详细表征长期的体液免疫和细胞免疫。感染后1年多的时间里均可检测到SARS-CoV-2特异性T细胞和抗体,这表明初次感染期间建立的免疫保护得以维持,并且在再次感染或感染新出现的变异株时可能预防严重疾病。此外,这些数据证明了通过过继转移从康复个体中分离出的功能性抗病毒T细胞对住院COVID-19患者进行免疫治疗的可能性。