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体液免疫反应和副作用如何取决于疫苗类型及既往新冠病毒感染情况。

How Humoral Response and Side Effects Depend on the Type of Vaccine and Past SARS-CoV-2 Infection.

作者信息

Stępień Monika, Zalewska Małgorzata, Knysz Brygida, Świątoniowska-Lonc Natalia, Jankowska-Polańska Beata, Łaczmański Łukasz, Piwowar Agnieszka, Kuźniarski Amadeusz

机构信息

Department of Infectious Diseases, Liver Diseases and Acquired Immune Deficiencies, Wroclaw Medical University, 50-367 Wroclaw, Poland.

Center for Research and Innovation, 4th Military Teaching Hospital, 50-981 Wroclaw, Poland.

出版信息

Vaccines (Basel). 2022 Jun 29;10(7):1042. doi: 10.3390/vaccines10071042.

Abstract

Since the end of December 2020, it has been possible to vaccinate against COVID-19. Our aim was to evaluate and compare the effectiveness of the vaccines available at the time of the mass vaccination program in Poland and also to look into the most common adverse side effects. Patients' anti-SARS-CoV-2 antibodies levels were checked before vaccination and after the first and after the second/last dose by the anti-SARS-CoV-2 QuantiVac ELISA (IgG) (EUROIMMUN MedicinischeLabordiagnostica AG; Luebeck; Germany) test. Before each blood collection, all patients filled out a questionnaire regarding experienced side effects. We observed that 100% of patients responded to the vaccinations. After the first dose, convalescents had much higher levels of anti-SARS-CoV-2 antibodies than naive patients, although after the second dose, 61 out of 162 convalescents (37.7%) had lower results than before. The comparison of immunological responses in the convalescents group after the first dose and in the naive group after the second dose showed that convalescents had higher antibody titers, which may suggest the possibility of changing the vaccination schedule for convalescents. The highest antibody titers after both the first and second doses were observed after Moderna shots. Fever was identified as a significant factor regarding higher levels of antibodies after the first and second doses of the vaccine.

摘要

自2020年12月底以来,已可接种新冠疫苗。我们的目的是评估和比较波兰大规模疫苗接种计划实施时可用疫苗的有效性,并研究最常见的不良副作用。通过抗SARS-CoV-2 QuantiVac ELISA(IgG)(EUROIMMUN Medicinische Labordiagnostica AG;吕贝克;德国)检测,在接种疫苗前、第一剂后以及第二剂/最后一剂后检查患者的抗SARS-CoV-2抗体水平。每次采血前,所有患者都填写了一份关于所经历副作用的问卷。我们观察到100%的患者对疫苗接种有反应。第一剂后,康复者的抗SARS-CoV-2抗体水平比未感染过的患者高得多,尽管第二剂后,162名康复者中有61名(37.7%)的检测结果比之前低。对康复者组第一剂后和未感染过组第二剂后的免疫反应进行比较显示,康复者的抗体滴度更高,这可能表明有可能改变康复者的疫苗接种计划。接种Moderna疫苗后,第一剂和第二剂后的抗体滴度均最高。发热被确定为第一剂和第二剂疫苗后抗体水平较高的一个重要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1fb/9324271/f0b33e0849d6/vaccines-10-01042-g001.jpg

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