Monoclonal Antibody Discovery (MAD) Lab, Fondazione Toscana Life Sciences, Siena, Italy.
VisMederi Research S.r.l., Siena, Italy.
Nat Commun. 2023 Mar 28;14(1):1734. doi: 10.1038/s41467-023-37422-y.
Severe acute respiratory syndrome 2 Omicron BA.4 and BA.5 are characterized by high transmissibility and ability to escape natural and vaccine induced immunity. Here we test the neutralizing activity of 482 human monoclonal antibodies isolated from people who received two or three mRNA vaccine doses or from people vaccinated after infection. The BA.4 and BA.5 variants are neutralized only by approximately 15% of antibodies. Remarkably, the antibodies isolated after three vaccine doses target mainly the receptor binding domain Class 1/2, while antibodies isolated after infection recognize mostly the receptor binding domain Class 3 epitope region and the N-terminal domain. Different B cell germlines are used by the analyzed cohorts. The observation that mRNA vaccination and hybrid immunity elicit a different immunity against the same antigen is intriguing and its understanding may help to design the next generation of therapeutics and vaccines against coronavirus disease 2019.
严重急性呼吸系统综合征 2 型奥密克戎 BA.4 和 BA.5 的特点是具有高传染性和逃避自然及疫苗诱导免疫的能力。在这里,我们测试了从接种两剂或三剂 mRNA 疫苗的人群或从感染后接种疫苗的人群中分离出来的 482 个人源单克隆抗体的中和活性。BA.4 和 BA.5 变体仅被约 15%的抗体中和。值得注意的是,三剂疫苗接种后分离出的抗体主要靶向受体结合域 1/2 类,而感染后分离出的抗体主要识别受体结合域 3 表位区域和 N 端结构域。分析队列使用不同的 B 细胞胚系。有趣的是,观察到 mRNA 疫苗接种和混合免疫对相同抗原产生不同的免疫反应,其理解可能有助于设计针对 2019 年冠状病毒病的下一代治疗药物和疫苗。