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接种阿斯利康新冠疫苗(ChAdOx1)的医护人员中抗刺突抗体的衰减:一项前瞻性纵向研究

Waning of Anti-spike Antibodies in AZD1222 (ChAdOx1) Vaccinated Healthcare Providers: A Prospective Longitudinal Study.

作者信息

Mishra Sanjeeb K, Pradhan Subrat K, Pati Sanghamitra, Sahu Sumanta, Nanda Rajiv K

机构信息

Community Medicine, Veer Surendra Sai Institute of Medical Sciences And Research, Sambalpur, IND.

Field Epidemiology, Indian Council of Medical Research, Chennai, IND.

出版信息

Cureus. 2021 Nov 25;13(11):e19879. doi: 10.7759/cureus.19879. eCollection 2021 Nov.

DOI:10.7759/cureus.19879
PMID:34976499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8712221/
Abstract

Introduction Coronavirus disease 2019 (COVID-19) vaccines are nothing short of a miracle story halting the pandemic across the globe. Nearly half of the global population has received at least one dose. Nevertheless, antibody levels in vaccinated people have shown waning, and breakthrough infections have occurred. Our study aims to measure antibody kinetics following AZD1222 (ChAdOx1) vaccination six months after the second dose and the factors affecting the kinetics. Materials and methods We conducted a prospective longitudinal study monitoring for six months after the second of two AZD1222 (ChAdOx1) vaccine doses in healthcare professionals and healthcare facility employees at Veer Surendra Sai Institute of Medical Sciences and Research (included doctors, nurses, paramedical staff, security and sanitary workers, and students). Two 0.5-mL doses of the vaccine were administered intramuscularly, containing 5 x 10 viral particles 28 to 30 days between doses. We collected blood samples one month after the first dose (Round 1), one month after the second dose (Round 2), and six months after the second dose (Round 3). We tested for immunoglobulin G (IgG) levels against the receptor-binding domain of the spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by chemiluminescence microparticle immunoassay. We conducted a linear mixed model analysis to study the antibody kinetics and influencing factors. Results Our study included 122 participants (mean age, 41.5 years; 66 men, 56 women). The geometric mean IgG titers were 138.01 binding antibody units (BAU)/mL in Round 1, 176.48 BAU/mL in Round 2, and 112.95 BAU/mL in Round 3. Seven participants showed seroreversion, and 11 had breakthrough infections. Eighty-six participants showed a substantial decline in antibody titer from Rounds 2 to 3. Persons aged 45 or older had higher mean titer than people aged younger than 45 years. Overweight and obese (BMI ≥ 25 kg/m) had a higher mean titer than average or underweight persons. The only significant predictor of IgG titers at six months was SARS-CoV-2 infection on mixed model analysis. Conclusion We found a substantial decline in antibody levels leading to seven cases of seroreversion in healthcare professionals who received the ChAdOx1 vaccine. History of prior COVID-19 was the only significant factor in antibody levels at six months. Seroreversion and breakthrough infection warrant further research into the optimal timing and potential benefits of booster doses of the AZD1222 (ChAdOx1) COVID-19 vaccine.

摘要

引言 2019 冠状病毒病(COVID-19)疫苗堪称奇迹,阻止了全球范围内的大流行。全球近一半人口已接种至少一剂疫苗。然而,接种疫苗者体内的抗体水平已显示出下降,且出现了突破性感染。我们的研究旨在测量接种 AZD1222(ChAdOx1)疫苗第二剂六个月后的抗体动力学以及影响该动力学的因素。

材料与方法 我们在维尔·苏伦德拉·赛义德医学科学与研究学院对医护人员和医疗机构员工(包括医生、护士、辅助医疗人员、安保及卫生工作者和学生)进行了一项前瞻性纵向研究,在两剂 AZD1222(ChAdOx1)疫苗的第二剂接种后监测六个月。两剂 0.5 毫升的疫苗通过肌肉注射给药,每剂含 5×10 个病毒颗粒,两剂之间间隔 28 至 30 天。我们在第一剂接种后一个月(第 1 轮)、第二剂接种后一个月(第 2 轮)以及第二剂接种后六个月(第 3 轮)采集血样。我们通过化学发光微粒子免疫分析检测针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突蛋白受体结合域的免疫球蛋白 G(IgG)水平。我们进行了线性混合模型分析以研究抗体动力学及影响因素。

结果 我们的研究纳入了 122 名参与者(平均年龄 41.5 岁;男性 66 名;女性 56 名)。第 1 轮的几何平均 IgG 滴度为 138.01 结合抗体单位(BAU)/毫升,第 2 轮为 176.48 BAU/毫升,第 3 轮为 112.95 BAU/毫升。7 名参与者出现血清转化逆转,11 人发生突破性感染。86 名参与者的抗体滴度从第 2 轮至第 3 轮出现大幅下降。45 岁及以上人群的平均滴度高于 45 岁以下人群。超重和肥胖者(BMI≥25 kg/m²)的平均滴度高于平均体重或体重过轻者。混合模型分析显示,六个月时 IgG 滴度的唯一显著预测因素是 SARS-CoV-2 感染。

结论 我们发现,接种 ChAdOx1 疫苗的医护人员体内抗体水平大幅下降,导致 7 例血清转化逆转。既往 COVID-19 病史是六个月时抗体水平的唯一显著因素。血清转化逆转和突破性感染值得进一步研究 AZD1222(ChAdOx1)COVID-19 疫苗加强剂量的最佳时机和潜在益处。

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