Pereira Magno Luís Costa, Moreira Jessica Pronestino de Lima, Porto Luís Cristóvão, Souza Vania Maria Almeida de, Gonçalves Beatriz Cunta, Sampaio Amanda de Barros, Moutela Matheus Figueiredo, Farha Larissa Dos Reis, Esberard Bárbara Cathalá, Amorim Renata Fernandes de, Souza Heitor Siffert Pereira de, Carvalho Ana Teresa Pugas
Inflammatory Bowel Disease Outpatients Unit, Piquet Carneiro Polyclinic, Rio de Janeiro State University, Rio de Janeiro 20950-003, Brazil.
Department of Bromatology, Faculty of Pharmacy, Fluminense Federal University, Niterói 24241-002, Brazil.
Healthcare (Basel). 2023 Oct 19;11(20):2767. doi: 10.3390/healthcare11202767.
This study aimed to evaluate humoral responses after vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) of patients with inflammatory bowel disease (IBD). Patients with IBD enrolled in a tertiary outpatient unit were followed up between September 2021 and September 2022 via serial blood collection. Immunoglobulin G antibody titers against SARS-CoV-2 were measured before administration and 1 and 6 months after the administration of two doses of different vaccination regimens. The results were compared with those of a healthy control group obtained during the same period. The mean pre-vaccination antibody titers were 452.0 and 93.3 AU/mL in the IBD ( = 42) and control ( = 89) groups, respectively. After two doses of the vaccine, the titers significantly increased in both groups (IBD, 8568.0 AU/mL; control, 7471.0 AU/mL; < 0.001). One month after the second dose, no significant differences were observed between the two groups ( = 0.955). Significant differences between vaccination schemes in the IBD group were observed, with higher titers in those who received Pfizer, younger patients ( < 0.005), and those with a previous coronavirus disease 2019 (COVID-19) infection ( < 0.012). The use of immunosuppressants and immunobiologicals did not affect the overall humoral response to COVID-19 vaccine in patients with IBD, but specific vaccine regimens, age, and previous coronavirus infection significantly did. This study reinforces the positive impact of booster doses and the safety of SARS-CoV-2 vaccination.
本研究旨在评估炎症性肠病(IBD)患者接种严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗后的体液免疫反应。2021年9月至2022年9月期间,对一家三级门诊单位收治的IBD患者进行了连续采血随访。在接种两剂不同疫苗方案之前、接种后1个月和6个月,测量了针对SARS-CoV-2的免疫球蛋白G抗体滴度。将结果与同期获得的健康对照组结果进行比较。IBD组(n = 42)和对照组(n = 89)接种前的平均抗体滴度分别为452.0和93.3 AU/mL。接种两剂疫苗后,两组的滴度均显著升高(IBD组为8568.0 AU/mL;对照组为7471.0 AU/mL;P < 0.001)。在第二剂接种后1个月,两组之间未观察到显著差异(P = 0.955)。在IBD组中,观察到不同疫苗接种方案之间存在显著差异,接种辉瑞疫苗的患者、年轻患者(P < 0.005)以及既往有2019冠状病毒病(COVID-19)感染的患者(P < 0.012)抗体滴度更高。使用免疫抑制剂和免疫生物制剂并不影响IBD患者对COVID-19疫苗的总体体液免疫反应,但特定的疫苗接种方案、年龄和既往冠状病毒感染显著影响该反应。本研究强化了加强针的积极影响以及SARS-CoV-2疫苗接种的安全性。