Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.
Division of Allergy and Infectious Diseases, University of Washington, Seattle, WA 98195, USA.
Immunity. 2024 Apr 9;57(4):904-911.e4. doi: 10.1016/j.immuni.2024.02.016. Epub 2024 Mar 14.
Immune imprinting describes how the first exposure to a virus shapes immunological outcomes of subsequent exposures to antigenically related strains. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) Omicron breakthrough infections and bivalent COVID-19 vaccination primarily recall cross-reactive memory B cells induced by prior Wuhan-Hu-1 spike mRNA vaccination rather than priming Omicron-specific naive B cells. These findings indicate that immune imprinting occurs after repeated Wuhan-Hu-1 spike exposures, but whether it can be overcome remains unclear. To understand the persistence of immune imprinting, we investigated memory and plasma antibody responses after administration of the updated XBB.1.5 COVID-19 mRNA vaccine booster. We showed that the XBB.1.5 booster elicited neutralizing antibody responses against current variants that were dominated by recall of pre-existing memory B cells previously induced by the Wuhan-Hu-1 spike. Therefore, immune imprinting persists after multiple exposures to Omicron spikes through vaccination and infection, including post XBB.1.5 booster vaccination, which will need to be considered to guide future vaccination.
免疫印记描述了初次接触病毒如何影响随后接触抗原相关株的免疫结果。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)奥密克戎突破性感染和二价 COVID-19 疫苗接种主要召回先前武汉-Hu-1 刺突 mRNA 疫苗接种诱导的交叉反应性记忆 B 细胞,而不是启动奥密克戎特异性幼稚 B 细胞。这些发现表明,免疫印记发生在多次武汉-Hu-1 刺突暴露之后,但是否可以克服仍不清楚。为了了解免疫印记的持久性,我们研究了接种更新的 XBB.1.5 COVID-19 mRNA 疫苗加强针后记忆和血浆抗体反应。我们表明,XBB.1.5 加强针针对当前变体产生了中和抗体反应,这些反应主要是由先前武汉-Hu-1 刺突诱导的预先存在的记忆 B 细胞的回忆引起的。因此,通过接种和感染(包括 XBB.1.5 加强针接种后)对奥密克戎刺突进行多次暴露后,免疫印记仍然存在,这将需要考虑以指导未来的疫苗接种。