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mRNA 新冠疫苗接种对既往 SARS-CoV-2 感染者和未感染者适应性免疫应答动力学的影响。

Kinetics of adaptive immune responses after administering mRNA-Based COVID-19 vaccination in individuals with and without prior SARS-CoV-2 infections.

机构信息

Department of Biological Science and Biotechnology, Andong National University, Andong, 36729, Korea.

Gyeongsang Institute of Health Sciences, Gyeongsang National University, Jinju, 52727, Korea.

出版信息

BMC Infect Dis. 2023 Oct 27;23(1):732. doi: 10.1186/s12879-023-08728-5.

DOI:10.1186/s12879-023-08728-5
PMID:37891503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10604405/
Abstract

OBJECTIVE

We aimed to compare the adaptive immune response in individuals with or without prior SARS-CoV-2 infections following the administration of mRNA-based COVID-19 vaccines.

METHODS

A total of 54 participants with ages ranging from 37 to 56 years old, consisting of 23 individuals without a history of SARS-CoV-2 infection (uninfected group) and 31 individuals with prior infection of SARS-CoV-2 (infected group) who have received two doses of mRNA SARS-CoV-2 vaccines were enrolled in this study. We measured the IFN-γ level upon administration of BNT162b2 (PF) or mRNA-1273 (MO) by QuantiFERON SARS-CoV-2. The production of neutralizing antibodies was evaluated by a surrogate virus neutralization assay, and the neutralizing capacity was assessed by a plaque reduction neutralization test (PRNT). The immune response was compared between the two groups.

RESULTS

A significantly higher level of IFN-γ (p < 0.001) and neutralization antibodies (p < 0.001) were observed in the infected group than those in the uninfected group following the first administration of vaccines. The infected group demonstrated a significantly higher PRNT titer than the uninfected group against the Wuhan strain (p < 0.0001). Still, the two groups were not significantly different against Delta (p = 0.07) and Omicron (p = 0.14) variants. Following the second vaccine dose, T- and B-cell levels were not significantly increased in the infected group.

CONCLUSION

A single dose of mRNA-based COVID-19 vaccines would boost immune responses in individuals who had previously contracted SARS-CoV-2.

摘要

目的

本研究旨在比较既往感染 SARS-CoV-2 人群与无感染史人群在接种 mRNA 新冠疫苗后的适应性免疫反应。

方法

本研究共纳入 54 名年龄在 37 至 56 岁之间的参与者,其中 23 名无 SARS-CoV-2 感染史(未感染组),31 名既往感染过 SARS-CoV-2(感染组),均接种了两剂 mRNA SARS-CoV-2 疫苗。我们通过 QuantiFERON SARS-CoV-2 检测接种 BNT162b2(PF)或 mRNA-1273(MO)时 IFN-γ 的水平。通过假病毒中和试验评估中和抗体的产生,并用蚀斑减少中和试验(PRNT)评估中和能力。比较两组间的免疫反应。

结果

与未感染组相比,感染组在接种疫苗后首次给药时 IFN-γ(p<0.001)和中和抗体(p<0.001)水平显著升高。感染组对武汉株的 PRNT 滴度显著高于未感染组(p<0.0001)。然而,两组对 Delta(p=0.07)和 Omicron(p=0.14)变异株的差异无统计学意义。接种第二剂疫苗后,感染组 T 细胞和 B 细胞水平无显著升高。

结论

单次接种 mRNA 新冠疫苗可增强既往感染 SARS-CoV-2 人群的免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/517e23cb1329/12879_2023_8728_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/ec74cab88b3c/12879_2023_8728_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/d43fedb11396/12879_2023_8728_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/cd629605fe03/12879_2023_8728_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/517e23cb1329/12879_2023_8728_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/ec74cab88b3c/12879_2023_8728_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/d43fedb11396/12879_2023_8728_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/cd629605fe03/12879_2023_8728_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea84/10604405/517e23cb1329/12879_2023_8728_Fig4_HTML.jpg

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2
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3
Post-vaccination T cell immunity to omicron.
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BMC Infect Dis. 2025 Mar 11;25(1):342. doi: 10.1186/s12879-025-10754-4.
4
Validation of the Enzyme-Linked ImmunoSpot Analytic Method for the Detection of Human IFN-γ from Peripheral Blood Mononuclear Cells in Response to the SARS-CoV-2 Spike Protein.酶联免疫斑点分析法检测外周血单个核细胞中 SARS-CoV-2 刺突蛋白诱导的人 IFN-γ的验证。
Biomolecules. 2024 Oct 11;14(10):1286. doi: 10.3390/biom14101286.
奥密克戎疫苗接种后的 T 细胞免疫。
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7
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9
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10
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