Development of a two-component recombinant vaccine for COVID-19.

IF 5.9 2区 医学 Q1 IMMUNOLOGY Frontiers in Immunology Pub Date : 2024-12-20 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1514226
Yi-Sheng Sun, Fang Xu, Han-Ping Zhu, Yong Xia, Qiao-Min Li, Yuan-Yuan Luo, Hang-Jing Lu, Bei-Bei Wu, Zhen Wang, Ping-Ping Yao, Zhan Zhou
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Abstract

Introduction: Though COVID-19 as a public health emergency of international concern (PHEIC) was declared to be ended by the WHO, it continues to pose a significant threat to human society. Vaccination remains one of the most effective methods for preventing COVID-19. While most of the antigenic regions are found in the receptor binding domain (RBD), the N-terminal domain (NTD) of the S protein is another crucial region for inducing neutralizing antibodies (nAbs) against COVID-19.

Methods: In the two-dose immunization experiment, female BALB/c mice were intramuscularly immunized with different ratios of RBD-Fc and NTD-Fc proteins, with a total protein dose of 8 μg per mouse. Mice were immunized on day 0 and boosted on day 7. In the sequential immunization experiment, groups of female BALB/c mice were immunized with two doses of the inactivated SARS-CoV-2 vaccine (prototype strain) on day 0 and 7. On day 28, mice were boosted with RBD-Fc, NTD-Fc, RBD-Fc/NTD-Fc (9:1), RBD-Fc/NTD-Fc (3:1), inactivated SARS-CoV-2 vaccine (protoype strain), inactivated SARS-CoV-2 vaccine (omicron strain), individually. The IgG antibodies were detected using ELISA, while the neutralizing antibodies were measured through a microneutralization assay utilizing both the prototype and omicron strains. The ELISPOT assays were performed to measure the secretion of IL-4 and IFN-γ, and the concentrations of secreted IL-2 and IL-10 in the supernatants were measured by ELISA.

Results: We have first developed a two-component recombinant vaccine for COVID-19 based on RBD-Fc and NTD-Fc proteins, with an optimal RBD-Fc/NTD-Fc ratio of 3:1. This novel two-component vaccine demonstrated the ability to induce durable and potent IgG antibodies, as well as the neutralizing antibodies in both the two-dose homologous and sequential vaccinations. Heterologous booster with this two-component vaccine could induce higher neutralizing antibody titers than the homologous group. Additionally, the vaccine elicited relatively balanced Th1- and Th2-cell immune responses.

Conclusion: This novel two-component recombinant vaccine exhibits high immunogenicity and offers a potential booster strategy for COVID-19 vaccine development.

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新型冠状病毒双组分重组疫苗的研制
导言:尽管世界卫生组织宣布 COVID-19 作为国际关注的突发公共卫生事件(PHEIC)已经结束,但它仍对人类社会构成重大威胁。接种疫苗仍是预防 COVID-19 的最有效方法之一。虽然大部分抗原区域位于受体结合域(RBD),但 S 蛋白的 N 端域(NTD)是诱导 COVID-19 中和抗体(nAbs)的另一个关键区域:在两剂量免疫实验中,雌性BALB/c小鼠肌肉注射不同比例的RBD-Fc和NTD-Fc蛋白,每只小鼠的蛋白总剂量为8 μg。小鼠在第0天进行免疫,第7天进行强化。在连续免疫实验中,每组雌性 BALB/c 小鼠分别在第 0 天和第 7 天接种两剂 SARS-CoV-2 灭活疫苗(原型株)。第 28 天,分别用 RBD-Fc、NTD-Fc、RBD-Fc/NTD-Fc(9:1)、RBD-Fc/NTD-Fc(3:1)、SARS-CoV-2 灭活疫苗(原型株)、SARS-CoV-2 灭活疫苗(奥米克隆株)对小鼠进行强化。IgG 抗体采用 ELISA 法检测,中和抗体则采用原型株和奥米克龙株的微中和法测定。用 ELISPOT 法检测 IL-4 和 IFN-γ 的分泌,用 ELISA 法检测上清液中分泌的 IL-2 和 IL-10 的浓度:我们首次开发出了一种基于RBD-Fc和NTD-Fc蛋白的COVID-19双组分重组疫苗,其最佳RBD-Fc/NTD-Fc比例为3:1。这种新型双组分疫苗在两剂同源接种和连续接种中均能诱导出持久、强效的 IgG 抗体以及中和抗体。使用这种双组分疫苗的异源强化免疫比同源组能诱导出更高的中和抗体滴度。此外,该疫苗还能引起相对平衡的 Th1 和 Th2 细胞免疫反应:结论:这种新型双组分重组疫苗具有很高的免疫原性,为 COVID-19 疫苗的开发提供了一种潜在的增效策略。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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