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一种用于新型冠状病毒肺炎的双组分重组疫苗的研发。

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

作者信息

Sun Yi-Sheng, Xu Fang, Zhu Han-Ping, Xia Yong, Li Qiao-Min, Luo Yuan-Yuan, Lu Hang-Jing, Wu Bei-Bei, Wang Zhen, Yao Ping-Ping, Zhou Zhan

机构信息

Zhejiang Key Lab of Vaccine, Infectious Disease Prevention and Control, Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, China.

Innovation Institute for Artificial Intelligence in Medicine and Zhejiang Provincial Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

出版信息

Front Immunol. 2024 Dec 20;15:1514226. doi: 10.3389/fimmu.2024.1514226. eCollection 2024.

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.

摘要

引言

尽管世界卫生组织宣布将新型冠状病毒肺炎(COVID-19)这一国际关注的突发公共卫生事件(PHEIC)结束,但它仍继续对人类社会构成重大威胁。接种疫苗仍然是预防COVID-19最有效的方法之一。虽然大部分抗原区域位于受体结合域(RBD),但刺突蛋白的N端结构域(NTD)是诱导针对COVID-19的中和抗体(nAbs)的另一个关键区域。

方法

在两剂免疫实验中,将雌性BALB/c小鼠用不同比例的RBD-Fc和NTD-Fc蛋白进行肌肉注射免疫,每只小鼠的总蛋白剂量为8μg。小鼠在第0天免疫,并在第7天加强免疫。在序贯免疫实验中,雌性BALB/c小鼠组在第0天和第7天用两剂灭活的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗(原型株)进行免疫。在第28天,小鼠分别用RBD-Fc、NTD-Fc、RBD-Fc/NTD-Fc(9:1)、RBD-Fc/NTD-Fc(3:1)、灭活的SARS-CoV-2疫苗(原型株)、灭活的SARS-CoV-2疫苗(奥密克戎株)进行加强免疫。使用酶联免疫吸附测定(ELISA)检测IgG抗体,同时通过使用原型株和奥密克戎株的微量中和试验测量中和抗体。进行酶联免疫斑点试验(ELISPOT)以测量白细胞介素-4(IL-4)和干扰素-γ(IFN-γ)的分泌,并通过ELISA测量上清液中分泌的IL-2和IL-10的浓度。

结果

我们首次基于RBD-Fc和NTD-Fc蛋白开发了一种用于COVID-19的双组分重组疫苗,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和序贯接种中均表现出诱导持久且强效的IgG抗体以及中和抗体的能力。用这种双组分疫苗进行异源加强免疫可诱导比同源组更高的中和抗体滴度。此外,该疫苗引发了相对平衡的Th1和Th2细胞免疫反应。

结论

这种新型双组分重组疫苗具有高免疫原性,并为COVID-19疫苗开发提供了一种潜在的加强免疫策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a518/11695372/951fda1f250c/fimmu-15-1514226-g001.jpg

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