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使用即时护理替代中和试验评估疫苗诱导的严重急性呼吸综合征冠状病毒 2 效应的异质性。

Heterogeneity assessment of vaccine-induced effects using point-of-care surrogate neutralization test for severe acute respiratory syndrome coronavirus 2.

机构信息

Kawasaki Physicians Association, Kawasaki, Japan.

Department of Internal Medicine, Kawasaki Rinko General Hospital, Kawasaki, Japan.

出版信息

J Clin Lab Anal. 2022 Jul;36(7):e24545. doi: 10.1002/jcla.24545. Epub 2022 Jun 9.

Abstract

INTRODUCTION

Coronavirus disease (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a global pandemic even after vaccination. We aimed to identify immunological heterogeneity over time in vaccinated healthcare workers using neutralization antibodies and neutralizing activity tests.

METHODS

Serum samples were collected from 214 healthcare workers before vaccination (pre) and on days 22, 90, and 180 after receiving the first dose of BNT162b2 vaccine (day 0). Neutralization antibody (NAb, SARS-CoV-2 S-RBD IgM/IgG) titers and two kinds of surrogate virus neutralization tests (sVNTs) were analyzed (UMIN000043851).

RESULTS

The NAb (SARS-CoV-2 S-RBD IgG) titer peaked on day 90 after vaccination (30,808.0 μg/ml ± 35,211; p < 0.0001) and declined on day 180 (11,678.0 μg/ml ± 33,770.0; p < 0.0001). The neutralizing activity also peaked on day 90 and declined with larger individual differences than those of IgG titer on day 180 (88.9% ± 15.0%, 64.8% ± 23.7%, p < 0.0001). We also found that the results of POCT-sVNT (immunochromatography) were highly correlated with those of conventional sVNT (ELISA).

CONCLUSIONS

Neutralizing activity is the gold standard for vaccine efficacy evaluation. Our results using conventional sVNT showed large individual differences in neutralizing activity reduction on day 180 (64.8% ± 23.7%), suggesting an association with the difference in vaccine efficacy. POCT-sVNT is rapid and user-friendly; it might be used for triage in homes, isolation facilities, and event venues without restrictions on the medical testing environment.

摘要

简介

由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的冠状病毒疾病(COVID-19)即使在接种疫苗后也已成为全球大流行。我们旨在使用中和抗体和中和活性试验来确定接种疫苗的医护人员随时间推移的免疫异质性。

方法

从 214 名医护人员接种疫苗前(预)和接种第一剂 BNT162b2 疫苗后第 22、90 和 180 天(第 0 天)采集血清样本。分析中和抗体(NAb,SARS-CoV-2 的 S-RBD IgM/IgG)滴度和两种替代病毒中和试验(sVNTs)(UMIN000043851)。

结果

接种后第 90 天 NAb(SARS-CoV-2 的 S-RBD IgG)滴度达到峰值(30,808.0μg/ml±35,211;p<0.0001),第 180 天下降(11,678.0μg/ml±33,770.0;p<0.0001)。中和活性也在第 90 天达到峰值,并在第 180 天显示出比 IgG 滴度更大的个体差异(88.9%±15.0%,64.8%±23.7%,p<0.0001)。我们还发现,POCT-sVNT(免疫层析法)的结果与常规 sVNT(ELISA)的结果高度相关。

结论

中和活性是疫苗功效评估的金标准。我们使用常规 sVNT 的结果表明,第 180 天中和活性下降的个体差异很大(64.8%±23.7%),这表明与疫苗功效的差异有关。POCT-sVNT 快速且易于使用;它可以在没有医疗检测环境限制的情况下用于家庭、隔离设施和活动场所的分诊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/307c/9279978/292cb112ba3b/JCLA-36-e24545-g005.jpg

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