Department of General Internal Medicine, Hirata Central Hospital, Hirata, Ishikawa District, Fukushima, Japan.
Department of Radiation Health Management, Fukushima Medical University School of Medicine, Fukushima City, Fukushima, Japan.
PLoS One. 2022 Jun 10;17(6):e0269917. doi: 10.1371/journal.pone.0269917. eCollection 2022.
The purpose of this study was to identify factors associated with the increase in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S1) protein and neutralizing antibody titer following SARS-CoV-2 vaccination. This observational study was conducted among healthcare workers working for a private hospital group in Fukushima Prefecture, Japan. Two blood samples were obtained from each participant. The first sample was obtained before the first dose of BNT162b2 (Pfizer-BioNTech) vaccine, and a second sample was obtained approximately 6 weeks later. Immunoglobulin G (IgG) antibody against the SARS-CoV-2 spike (S1) protein, immunoglobulin M (IgM) antibody against SARS-CoV-2 N-protein, and neutralizing activity were measured using the chemiluminescent immunoassay with iFlash 3000. A total of 231 healthcare workers who agreed to participate, and were negative for anti-SARS-CoV-2 IgM antibodies at enrollment, were included in the analysis. All participants had elevated IgG antibodies and neutralizing activity above the cutoff values. A total of 174 (75.3%) and 208 (90.0%) participants experienced adverse reactions after the first and second vaccine doses, respectively. Younger age, female sex, not taking immunosuppressive or antipyretic analgesic medication regularly, a lack of local adverse reactions after the first dose, and the presence of adverse reactions (fever, muscle, and joint pain) after the second dose were associated with higher IgG antibody titers and neutralizing activity. Intake of analgesic antipyretic for adverse reactions to vaccines was not significantly associated with antibody and neutralizing activity titer production. Immune responses after vaccination may differ among individuals, and continued countermeasures to prevent SARS-CoV-2 infection are vital.
本研究旨在确定与接种严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突(S1)蛋白和中和抗体滴度升高相关的因素。这是一项在日本福岛县一家私立医院集团工作的医护人员中进行的观察性研究。每位参与者采集两份血样。第一份样本在接种 BNT162b2(辉瑞-生物技术)疫苗前采集,第二份样本大约在 6 周后采集。使用化学发光免疫分析法和 iFlash 3000 测定针对 SARS-CoV-2 刺突(S1)蛋白的 IgG 抗体、针对 SARS-CoV-2 N 蛋白的 IgM 抗体和中和活性。共有 231 名同意参加且在入组时抗 SARS-CoV-2 IgM 抗体阴性的医护人员纳入分析。所有参与者的 IgG 抗体和中和活性均高于临界值。第一次和第二次疫苗接种后,分别有 174(75.3%)和 208(90.0%)名参与者出现不良反应。年龄较小、女性、不规律服用免疫抑制剂或解热镇痛药物、第一次接种后无局部不良反应以及第二次接种后出现不良反应(发热、肌肉和关节疼痛)与更高的 IgG 抗体滴度和中和活性相关。接种疫苗后的不良反应服用解热镇痛药物与抗体和中和活性滴度产生无显著相关性。接种疫苗后的免疫反应可能因人而异,因此继续采取措施预防 SARS-CoV-2 感染至关重要。