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评估个体、序贯和联合接种策略诱导的来自野生型和新兴变异株的不同 SARS-CoV-2 刺突三聚体产生的体液免疫反应。

Evaluation of humoral immune responses induced by different SARS-CoV-2 spike trimers from wild-type and emerging variants with individual, sequential, and combinational delivered strategies.

机构信息

The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.

Department of Microbiology, Anhui Provincial Center for Disease Control and Prevention, Hefei, Anhui, China.

出版信息

J Med Virol. 2022 Dec;94(12):5841-5849. doi: 10.1002/jmv.28081. Epub 2022 Aug 29.

Abstract

The spike trimer of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an effective target for inducing neutralizing antibodies by coronavirus disease 2019 (COVID-19) vaccines. However, the diversity of spike protein from emerging SASR-CoV-2 variants has become the major challenge for development of a universal vaccine. To investigate the immunogenicity of spike proteins from various circulating strains including wild type, Delta, and Omicron variants, we produced various natural spike trimers and designed three vaccination strategies, that is, individual, sequential, and bivalent regimens to assess autologous and heterogenous antibody responses in a mouse model. The results indicated that monovalent vaccine strategy with individual spike trimer could only induce binding and neutralizing antibodies against homologous viruses. However, sequential and bivalent immunization with Delta and Omicron spike trimers could induce significantly broader neutralizing antibody responses against heterogenous SARS-CoV-2. Interestingly, the spike trimer from Omicron variant showed superior immunogenicity in inducing antibody response against recently emerging XE variant. Taken together, our data supported the development of novel vaccination strategies or multivalent vaccine against emerging variants.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的刺突三聚体是诱导 2019 年冠状病毒病(COVID-19)疫苗产生中和抗体的有效靶点。然而,新兴 SARS-CoV-2 变体的刺突蛋白多样性已成为开发通用疫苗的主要挑战。为了研究包括野生型、Delta 和奥密克戎变体在内的各种流行 SARS-CoV-2 株的刺突蛋白的免疫原性,我们制备了各种天然刺突三聚体,并设计了三种疫苗接种策略,即个体、序贯和双价方案,以在小鼠模型中评估同源和异源抗体反应。结果表明,单价疫苗策略用单个刺突三聚体只能诱导针对同源病毒的结合和中和抗体。然而,Delta 和奥密克戎刺突三聚体的序贯和双价免疫可诱导针对异源 SARS-CoV-2 的显著更广泛的中和抗体反应。有趣的是,奥密克戎变体的刺突三聚体在诱导针对最近出现的 XE 变体的抗体反应方面表现出更高的免疫原性。总之,我们的数据支持针对新兴变体开发新型疫苗接种策略或多价疫苗。

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