接种和自然感染SARS-CoV-2后对SARS-CoV-2刺突蛋白受体结合域的抗体应答

F. Rahman, Sraboni Mazumder, S. Farook, P. Deb, S. Saha, F. Akter, Md. Shariful Alam Jilani, J. Haq
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引用次数: 0

摘要

背景与目的:SARS-CoV-2抗体在自然感染SARS-CoV-2和疫苗接种后均可产生。本研究旨在确定自然感染SARS-CoV-2并接种疫苗后人群对SARS-CoV-2的抗体反应。材料与方法:研究对象为18岁及以上的成年人。研究人群由四组组成。1组(对照组):健康,无SARS-CoV-2感染史,未接种疫苗;2组:既往有SARS-CoV-2感染史,未接种疫苗;3组:既往无SARS-CoV-2感染史,接种2剂重组腺病毒载体疫苗ChAdOx1(牛津-阿斯利康);4组:既往有SARS-CoV-2感染史,接种2剂ChAdOx1疫苗。第3组和第4组分别于第二次接种后1和7个月采血。在入组时,从Gr-1和gr - 2参与者中采集单份血液样本。ELISA法检测血清中SARS-CoV-2刺突蛋白S1受体结合域(RBD)抗体(抗rbds1 IgG)。结果:共纳入176名18岁及以上的参与者。1组、2组、3组和4组抗rbds1 IgG阳性率分别为51.9%、66.7%、96.8%和100%。第2次接种1个月后,Gr-4组抗rbds1 IgG抗体水平(120.8±31.9 DU/ml)显著高于其他组(p < 0.05)。四组个体的抗体反应无显著差异,不分性别和合并症。第2次接种后7个月,3组和4组的抗体浓度分别下降85.3%(112.1±30.4 DU/ml至75.9±48.7 DU/ml)和81.5%(127.3±20.4 DU/ml至92.5±43.6 DU/ml)。7个月后抗体分别下降40.6%和34.7%,但除3组1例外均为阳性。发热(34.4%)和头痛(24.8%)是接种疫苗后最常见的不良反应。结论:ChAdOx1 nCoV-19疫苗在第2次接种后可诱导出高浓度的持续抗rbds1 IgG抗体,既往感染SARS-CoV-2可作为免疫启动物。因此,在加强剂量之前进行抗体筛选试验可能是一个很好的选择,以最大限度地提高疫苗接种的覆盖率。中华医学会医学杂志。2023;17(1): 009。DOI: https://doi.org/10.55010/imcjms.17.009*Correspondence: J. Ashraful Haq, Ibrahim医学院微生物系,1/A Ibrahim Sarani, Segunbagicha,孟加拉国达卡。电子邮件:jahaq54@yahoo.com
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Antibody response to receptor-binding domain of SARS-CoV-2 spike protein following vaccination and natural infection with SARS-CoV-2
Background and objectives: Antibody to SARS-CoV-2 develops both after natural infection with SARS-CoV-2 and vaccination. This study was undertaken to determine the antibody response to SARS-CoV-2 among population after natural SARS-CoV-2 infection and vaccination. Material and methods: The study was carried out on adults aged 18 years and above. Study population consisted of four groups. Group-1 (control): healthy and history of no prior SARS-CoV-2 infection and vaccination, Group-2: had past SARS-CoV-2 infection and no vaccination, Group-3: received two doses of recombinant adenoviral vector vaccine ChAdOx1 (Oxford–AstraZeneca) without past SARS-CoV-2 infection, and Group-4: had past SARS-CoV-2 infection and received 2 doses of ChAdOx1 vaccination. Blood was collected 1 and 7 months after the second dose of vaccination from Group-3 and 4 individuals. Single blood sample was collected from participants of Gr-1 and 2 at the time of enrolment. Immunoglobulin G (IgG) antibodies to receptor-binding domain (RBD) of SARS-CoV-2 spike protein S1 (anti-RBDS1 IgG) was determined in serum by ELISA method. Results: Total 176 participants aged 18 years and above were enrolled. Anti-RBDS1 IgG positivity rates were 51.9%, 66.7%, 96.8% and 100% in individuals of Group-1, 2, 3 and 4 respectively. Gr-4 had significantly (p < 0.05) mean higher anti-RBDS1 IgG antibody level (120.8 ± 31.9 DU/ml) compared to other groups 1 month after 2nd dose of vaccination. No significant differences in antibody response were found among the individuals of four groups across gender and comorbidities. Seven months after the 2nd dose of vaccines, the antibody concentration declined in 85.3% (112.1 ± 30.4 DU/ml to 75.9 ± 48.7 DU/ml) and 81.5% (127.3 ± 20.4 DU/ml to 92.5 ± 43.6 DU/ml) individuals of Group-3 and Group-4 respectively. Decline of antibody was 40.6% and 34.7% in 7 months, but all remained positive except 1 in Group-3. Fever (34.4%) and headache (24.8%) were the most common adverse effects noted after vaccination. Conclusion: The study revealed that ChAdOx1 nCoV-19 vaccine induces high concentration of persisting anti-RBDS1 IgG antibody after 2nd dose and previous infection with SARS-CoV-2 acts as immune priming. Therefore, antibody screening test prior to booster dose could be a good option to maximize coverage of vaccination. IMC J Med Sci. 2023; 17(1): 009. DOI: https://doi.org/10.55010/imcjms.17.009 *Correspondence: J. Ashraful Haq, Department of Microbiology, Ibrahim Medical College, 1/A Ibrahim Sarani, Segunbagicha, Dhaka, Bangladesh. Email: jahaq54@yahoo.com
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