Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Hum Vaccin Immunother. 2021 Oct 3;17(10):3551-3553. doi: 10.1080/21645515.2021.1929034. Epub 2021 May 25.
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.
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。