台湾地区接种疫苗医护人员SARS-CoV-2抗体的中和作用

Annals of medicine Pub Date : 2025-12-01 Epub Date: 2024-12-23 DOI:10.1080/07853890.2024.2442533
Seto Priyambodo, Kuang-Che Kuo, Ken-Pen Weng, Shih-Feng Liu, Guan-Da Syu, Ho-Chang Kuo
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引用次数: 0

摘要

背景:疫苗接种是控制SARS-CoV-2疫情的最佳途径之一。在台湾,卫生保健工作者优先接种疫苗,但这些疫苗对他们的有效性尚不清楚。因此,在初级强化疫苗接种后检查他们的中和抗体是必要的。方法:在这项前瞻性观察研究中,于2021年3月19日至2021年8月21日期间纳入了台湾长庚纪念医院的514名医护人员。两剂新冠病毒疫苗均为AZD1222与mRNA-1273的匹配或混合,即AZD1222 + AZD1222 (n = 406)、mRNA-1273 + mRNA-1273 (n = 62)和AZD1222 + mRNA-1273 (n = 46)。接种两剂疫苗后抽取血样,定义为疫苗后天数[中位数34.00天,四分位数范围(IQR) 29.00-42.00天],并通过SARS-CoV-2中和试剂盒检测中和抗体。在阴性对照的基础上,以抑制率的百分比对结果进行分析。结果:2次接种后,接种AZD1222 + mRNA-1273(中位数为97.15%,IQR为96.06 ~ 98.06%)和mRNA-1273 + mRNA-1273(中位数为97.47%,IQR为96.75 ~ 97.89%)的人比接种AZD1222 + AZD1222疫苗(中位数为71.28%,IQR为49.39 ~ 89.70%)的人表现出更高的中和抗体(该百分比指对替代病毒的抑制)。除了mRNA-1273 + mRNA-1273组外,接种后几天对中和抗体产生负影响。第二次给药后发热、头痛和肌痛的出现反映在较高的中和抗体中(无发热中位数76.00% vs发热中位数97.00%,p vs。头痛95.00%;肌痛96.00%,p。高血压56.00%,p = 0.0029;无癌中位数为81.00%,癌中位数为56.00%,p = 0.0143)。结论:推荐使用异源疫苗(AZD1222 + mRNA-1273)和2剂mRNA疫苗。对于未来的方向,我们需要调查疫苗接种对新的SARS-CoV-2变体的有效性。
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Neutralizing antibodies against SARS-CoV-2 of vaccinated healthcare workers in Taiwan.

Background: Vaccination is one of the best ways to control the SARS-CoV-2 outbreak. In Taiwan, healthcare workers were prioritized for vaccination, but the effectiveness of these vaccines for them remains unclear. Thus, it's essential to examine their neutralizing antibodies after prime-boost vaccinations.

Methods: In this prospective observational study, 514 healthcare workers from Chang Gung Memorial hospitals in Taiwan were included between 19 March 2021 and 21 August 2021. The two doses of COVID-19 vaccines were either a match or a mixing of AZD1222 and mRNA-1273, e.g. AZD1222 + AZD1222 (n = 406), mRNA-1273 + mRNA-1273 (n = 62), and AZD1222 + mRNA-1273 (n = 46). Blood specimens were drawn after two doses of vaccines, defined as post-vaccine days [median 34.00 days and interquartile range (IQR) 29.00-42.00 days], and examined for the neutralizing antibodies via SARS-CoV-2 neutralization kits. The results were analyzed as a percentage of inhibition based on the negative control.

Results: After 2 vaccination doses, subjects with AZD1222 + mRNA-1273 (median 97.15%, IQR 96.06-98.06%) and mRNA-1273 + mRNA-1273 (median 97.47%, IQR 96.75-97.89%) exhibited higher neutralizing antibodies than those receiving AZD1222 + AZD1222 vaccines (median 71.28%, IQR 49.39-89.70%) (the percentage was referred to inhibition of surrogate virus). The post-vaccination days negatively impacted the neutralizing antibodies, except for the mRNA-1273 + mRNA-1273 group. The presence of fever, headache, and myalgia after the second dosage was reflected in the higher neutralizing antibodies (median of no fever 76.00% vs. fever 97.00%, p < 0.0001; median of no headache 76.00% vs. headache 95.00%, p < 0.0001; median of no myalgia 75.50% vs. myalgia 96.00%, p < 0.0001). The subjects with underlying diseases, including hypertension and cancer showed lower neutralizing antibodies (median of no hypertension 81.00% vs. hypertension 56.00%, p = 0.0029; median of no cancer 81.00% vs. cancer 56.00%, p = 0.0143).

Conclusion: Heterologous prime-boost vaccines (AZD1222 + mRNA-1273) and two doses of mRNA vaccines are recommended. For future directions, we need to investigate the effectiveness of the vaccination against new SARS-CoV-2 variants.

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