Hammad Noha M, Kadry Heba M, Malek Mai M, Bahgat Shereen Mohamed, Abdelsalam Noha M, Afifi Amira Hamed Mohamed, Abo-Alella Doaa Alhussein
Department of Medical Microbiology and Immunology, Faculty of Medicine, Zagazig University, Zagazig 44519, Egypt.
Viral Infection Working Group of International Society of Antimicrobial Chemotherapy (VIWG/ISAC), England and Wales, UK.
Vaccines (Basel). 2022 Oct 12;10(10):1706. doi: 10.3390/vaccines10101706.
Background: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a constantly evolving virus, resulting in an increased burden on the existing COVID-19 vaccines. Healthcare workers (HCWs) are the first line of defense against the coronavirus disease 2019 (COVID-19) pandemic and have been prioritized among the risk categories receiving the COVID-19 vaccine. This work aimed to investigate the maintenance of antibody response of the Oxford−AstraZeneca vaccine (ChAdOx1/nCoV-19). Methods: Anti-spike immunoglobulin G (IgG) was measured at baseline point (immediately prior to vaccination) and 12- and 24-week (w) points following vaccination. Adverse reactions to the vaccine were reported. Participants were followed up for the incidence of COVID-19 during the 12 w interval between vaccination doses for 24 w after the second dose. Results: A total of 255 HCWs participated in the study. Prior to vaccination, 54.1% experienced COVID-19, 88.2% were seropositive after the first dose, while seropositivity reached 95.7% after the second dose. Following the first and second doses, the anti-spike IgG serum level was significantly higher in subjects with past COVID-19 than in others (p < 0.001 and =0.001, respectively). Conclusions: The Oxford−AstraZeneca vaccine is generally safe and provides a highly effective long-term humoral immune response against the Delta and Omicron variants of SARS-CoV-2.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是一种不断进化的病毒,给现有的2019冠状病毒病(COVID-19)疫苗带来了更大负担。医护人员(HCWs)是抗击2019冠状病毒病(COVID-19)大流行的第一道防线,在接受COVID-19疫苗的风险类别中被列为优先接种对象。这项研究旨在调查牛津-阿斯利康疫苗(ChAdOx1/nCoV-19)抗体反应的维持情况。方法:在基线点(接种疫苗前即刻)以及接种疫苗后的第12周和第24周测量抗刺突免疫球蛋白G(IgG)。报告疫苗的不良反应。在接种两剂疫苗之间的12周间隔内以及第二剂疫苗接种后24周内,对参与者随访COVID-19的发病率。结果:共有255名医护人员参与了该研究。接种疫苗前,54.1%的人感染过COVID-19,第一剂疫苗接种后88.2%的人血清呈阳性,而第二剂疫苗接种后血清阳性率达到95.7%。在接种第一剂和第二剂疫苗后,既往感染过COVID-19的受试者抗刺突IgG血清水平显著高于其他人(分别为p<0.001和=0.001)。结论:牛津-阿斯利康疫苗总体安全,对SARS-CoV-2的Delta和Omicron变异株可提供高效的长期体液免疫反应。