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辉瑞 COVID-19 疫苗接种后日本国立感染症研究所-国立卫生研究所员工的保护性疫苗接种后抗体水平。

The level of protective post-vaccination antibodies in NIPH-NIH employees after administration of Pfizer vaccine against COVID-19.

机构信息

National Institute of Public Health - National Institute of Hygiene, Department of Bacteriology and Biocontamination Control.

出版信息

Przegl Epidemiol. 2021;75(1):3-13. doi: 10.32394/pe.75.01.

Abstract

INTRODUCTION

The new SARS-CoV-2 coronavirus, first recognized in China in 2019, within a few months caused a global pandemic of a disease called COVID-19. The high incidence and mortality of COVID-19 was the reason for the beginning of intensive work on the development of an effective vaccine. In Poland, mass vaccinations against this disease began at the end of December 2020.

OBJECTIVES

The aim of the presented study was to determine the effectiveness of stimulating the production of specific antibodies for SARS-CoV-2 by the Pfizer vaccine.

MATERIAL AND METHODS

The presence of IgA and IgG antibodies to the spike (S protein) of SARSCoV-2 was tested by the ELISA/Euroimmun in serum samples obtained from 140 the employees of NIPH-NIH (137 were vaccinated). In addition, the presence of IgG antibodies to S protein, nucleoprotein, and mixture of both in selected serum samples was tested by the newly developed in NIPH-NIH in-house ELISA assay.

RESULTS

IgA and IgG antibodies to the S protein of the SARS-CoV-2 were detected by ELISA/Euroimmun, respectively in 136 and in all 137 vaccinated persons. There were no statistically significant differences in the level of antibodies depending on the sex and age of the vaccinated persons. Slightly higher levels of antibodies have been demonstrated in vaccinated subjects with documented preexisting SARS-CoV-2 immunity compared to subjects without COVID-19 history. The presence of IgA and IgG antibodies was found in respectively, 18 (45.0%) and all 40 (100.0%) tested vaccinated persons by the in-house ELISA with mixture antigen. The study showed that ELISA assay with N protein as an antigen may enable the distinction between antibodies acquired after infection and after vaccination.

CONCLUSIONS

The results obtained in the presented study clearly demonstrate the high effectiveness of the Pfizer vaccine in stimulation of the human immune system to produce antibodies specific for the S protein of the SARS-CoV-2. It is necessary to continue testing vaccine antibody levels at various times after vaccination to determine the potential duration of humoral immunity.

摘要

简介

2019 年在中国首次发现的新型 SARS-CoV-2 冠状病毒,在短短几个月内引发了 COVID-19 疾病的全球大流行。COVID-19 的高发病率和死亡率是开始积极开发有效疫苗的原因。在波兰,于 2020 年 12 月底开始对这种疾病进行大规模疫苗接种。

目的

本研究旨在确定辉瑞疫苗刺激 SARS-CoV-2 特异性抗体产生的效果。

材料和方法

通过 ELISA/Euroimmun 在 140 名 NIPH-NIH 员工(137 人接种疫苗)的血清样本中检测到针对 SARSCoV-2 刺突(S 蛋白)的 IgA 和 IgG 抗体。此外,在选定的血清样本中,通过 NIPH-NIH 新开发的内部 ELISA 检测试剂盒检测了针对 S 蛋白、核蛋白和两者混合物的 IgG 抗体的存在。

结果

通过 ELISA/Euroimmun 分别在 136 名和所有 137 名接种疫苗的个体中检测到针对 SARS-CoV-2 S 蛋白的 IgA 和 IgG 抗体。接种疫苗者的性别和年龄与抗体水平无统计学差异。与没有 COVID-19 病史的个体相比,具有已记录的 SARS-CoV-2 既往感染史的接种者中,抗体水平略高。在 18 名(45.0%)和 40 名(100.0%)接受测试的接种者中,通过内部混合抗原 ELISA 检测到 IgA 和 IgG 抗体的存在。研究表明,使用 N 蛋白作为抗原的 ELISA 检测方法可以区分感染后和接种后获得的抗体。

结论

本研究中获得的结果清楚地表明,辉瑞疫苗在刺激人体免疫系统产生针对 SARS-CoV-2 S 蛋白的特异性抗体方面具有很高的效果。有必要在接种后不同时间继续测试疫苗抗体水平,以确定体液免疫的潜在持续时间。

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