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接种BNT162b2或ChAdOx1新冠疫苗的医护人员血清抗体反应比较及不良反应分析

Serum Antibody Response Comparison and Adverse Reaction Analysis in Healthcare Workers Vaccinated with the BNT162b2 or ChAdOx1 COVID-19 Vaccine.

作者信息

Lim Sung-Hee, Choi Seong-Hyeok, Kim Bora, Kim Ji-Youn, Ji Young-Sok, Kim Se-Hyung, Kim Chan-Kyu, Kim Tark, Choo Eun-Ju, Moon Ji-Eun, Yun Jina, Park Seong-Kyu

机构信息

Department of Medicine, Division of Hematology-Oncology, Soonchunhyang University Bucheon Hospital, Bucheon 14584, Korea.

Department of Medicine, Division of Infectious Disease, Soonchunhyang University Bucheon Hospital, Bucheon 14584, Korea.

出版信息

Vaccines (Basel). 2021 Nov 24;9(12):1379. doi: 10.3390/vaccines9121379.

Abstract

The COVID-19 pandemic is changing rapidly and requires different strategies to maintain immunization. In Korea, different COVID-19 vaccines are recommended and available for various populations, including healthcare workers (HCWs) at high risk of SARS-CoV-2 infection. We plan to evaluate the adverse events (AEs) and immunogenicity of the BNT162b2 and ChAdOx1 vaccines in HCWs at a single center. This cohort study included HCWs fully vaccinated with either BNT162b2 or ChAdOx1. Blood samples were taken eight weeks after the second vaccination with both COVID-19 vaccines and six months after the second vaccination from participants with the BNT162b2 vaccine. The primary endpoint for immunogenicity was the serum neutralizing antibody responses eight weeks after vaccination. The secondary endpoint was the incidence of various AEs within 28 days of each vaccination. Between 16 March and 23 June 2021, 115 participants were enrolled (65 in the ChAdOx1 group and 50 in the BNT162b2 group). Significantly higher surrogate virus neutralization test (sVNT) inhibition was observed in participants vaccinated with two doses of BNT162b2 (mean (SD) 91.4 (9.68)%) than in those vaccinated with ChAdOx1 (mean (SD) 73.3 (22.57)%). The effectiveness of the BNT162b2 vaccine was maintained across all age and gender categories. At six months after the second dose, serum antibody levels declined significantly in the BNT162b2 group. The main adverse events, including fever, myalgia, fatigue, and headache, were significantly higher in the ChAdOx1 group after the first dose, whereas, after the second dose, those AEs were significantly higher in the BNT162b2 group ( < 0.05). Two doses of either the ChAdOx1 or the BNT162b2 COVID-19 vaccine resulted in very high seropositivity among the HCWs at our center. The quality of the antibody response, measured by sVNT inhibition, was significantly better with the BNT162b2 vaccine than with the ChAdOx1 vaccine. There was no significant association between neutralizing antibody response and AE after each vaccination in our cohort.

摘要

新型冠状病毒肺炎(COVID-19)大流行正在迅速变化,需要采取不同策略来维持免疫接种。在韩国,针对包括有严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染高风险的医护人员(HCW)在内的不同人群,推荐并提供了不同的COVID-19疫苗。我们计划在单一中心评估BNT162b2和ChAdOx1疫苗在医护人员中的不良事件(AE)和免疫原性。这项队列研究纳入了完全接种BNT162b2或ChAdOx1疫苗的医护人员。在接种两种COVID-19疫苗的第二次接种后8周以及接种BNT162b2疫苗的参与者第二次接种后6个月采集血样。免疫原性的主要终点是接种后8周的血清中和抗体反应。次要终点是每次接种后28天内各种不良事件的发生率。在2021年3月16日至6月23日期间,共招募了115名参与者(ChAdOx1组65名,BNT162b2组50名)。接种两剂BNT162b2的参与者中观察到的替代病毒中和试验(sVNT)抑制率显著高于接种ChAdOx1的参与者(平均值(标准差)91.4(9.68)%比73.3(22.57)%)。BNT162b2疫苗的有效性在所有年龄和性别类别中均得以维持。在第二次接种后6个月,BNT162b2组的血清抗体水平显著下降。主要不良事件,包括发热、肌痛、疲劳和头痛,在ChAdOx1组第一次接种后显著更高,而在第二次接种后,这些不良事件在BNT162b2组显著更高(<0.05)。两剂ChAdOx1或BNT162b2 COVID-19疫苗在我们中心的医护人员中均导致了非常高的血清阳性率。通过sVNT抑制测量的抗体反应质量,BNT162b2疫苗显著优于ChAdOx1疫苗。在我们的队列中,每次接种后中和抗体反应与不良事件之间无显著关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df5b/8708890/29bc392a7c0c/vaccines-09-01379-g001.jpg

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