Papadokostaki Eleni, Tentolouris Anastasios, Anastasiou Ioanna A, Psichogiou Mina, Iliaki Evangelia, Eleftheriadou Ioanna, Hatzakis Angelos, Tentolouris Nikolaos
Diabetes Center, First Department of Propaedeutic Internal Medicine, Medical School, National and Kapodistrian University of Athens, Laiko General Hospital, 115 27 Athens, Greece.
Department of Internal Medicine, University Hospital of Heraklion, 715 00 Heraklion, Greece.
Vaccines (Basel). 2022 Mar 2;10(3):382. doi: 10.3390/vaccines10030382.
The mRNA-based BNT162b2 vaccine has demonstrated high efficacy against severe SARS-CoV-2. However, data regarding immune response in people with diabetes mellitus (DM) after vaccination with the BNT162b2 vaccine are limited. In this prospective observational study, we examined humoral immune response in participants with and without DM after vaccination with the BNT162b2 mRNA vaccine. A total of 174 participants (58 with and 116 without diabetes, matched for age) were included. Antibodies were measured 21 days after the first dose, 7−15 days after the second dose, and 70−75 days after the second and before the third dose of the vaccine. Antibodies were measured by an anti-SARS-CoV-2 receptor-binding domain IgG (Abs-RBD-IgG) assay by a chemiluminescent microparticle immune assay; values > 50 AU/mL are considered protective from severe disease. Almost 17% of participants with DM did not develop adequate humoral immune response to the BNT162b2 mRNA vaccine after the first dose; however, it was high and similar after the second dose in both participants with and without DM and remained so almost 2 months after the second dose of the vaccine. Geometric mean values of Abs-RBD-IgG were not significantly different between participants with and without DM during the study. At least two doses of the BNT162b2 vaccine are necessary to ensure adequate and sustainable immune response in people with DM.
基于信使核糖核酸的BNT162b2疫苗已证明对严重的新型冠状病毒2具有高效性。然而,关于糖尿病患者接种BNT162b2疫苗后的免疫反应数据有限。在这项前瞻性观察研究中,我们检测了接种BNT162b2信使核糖核酸疫苗后糖尿病患者和非糖尿病患者的体液免疫反应。共纳入174名参与者(58名患有糖尿病,116名未患糖尿病,年龄匹配)。在接种第一剂疫苗后21天、第二剂疫苗后7至15天以及第二剂疫苗后且第三剂疫苗前70至75天测量抗体。通过化学发光微粒免疫分析的抗新型冠状病毒2受体结合域免疫球蛋白G(Abs-RBD-IgG)检测法测量抗体;值>50 AU/mL被认为对严重疾病具有保护作用。近17%的糖尿病患者在接种第一剂BNT162b2信使核糖核酸疫苗后未产生足够的体液免疫反应;然而,在接种第二剂疫苗后,糖尿病患者和非糖尿病患者的体液免疫反应都很高且相似,并且在接种第二剂疫苗后近2个月仍保持如此。在研究期间,糖尿病患者和非糖尿病患者的Abs-RBD-IgG几何平均值无显著差异。至少需要两剂BNT162b2疫苗才能确保糖尿病患者产生足够且持续的免疫反应。