Xu Xiaolin, Wang Luquan, Sun Yixin, Yang Changqing, Wang Xiaoling, Guo Peng, Mei Dong
Department of Pharmacy, Beijing Children's Hospital, National Center for Children's Health, Capital Medical University, Beijing, 100045, China.
School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Eur J Pediatr. 2025 May 3;184(5):324. doi: 10.1007/s00431-025-06152-2.
The increasing use of tumor necrosis factor inhibitors (TNFi) in pediatric patients has raised concerns about their potential impact on the immune system and related adverse events. Infection-related adverse events (AEs) caused by TNFi have already raised widespread concerns in real-world settings. This study aims to comprehensively analyze and summarize the infection-related AEs associated with TNFi in pediatric patients. A retrospective pharmacovigilance study was conducted to identify cases of TNFi-related infections reported to the FDA Adverse Event Reporting System (FAERS) database between Q1 2004 and Q1 2023. TNFi reports were carefully reviewed to exclude confounding factors like other AEs, concomitant medications, and prescription indications. Proportionality analysis was conducted by comparing TNFi reports to the entire FAERS database to identify infection-related AEs significantly associated with TNFi use. Infection-related AEs accounted for 8.36% of all TNFi-related adverse event reports in the FAERS database. A total of 8050 cases of TNFi-associated infections were identified in the pediatric population, with 2.57% of reports resulting in fatalities. Infliximab and golimumab showed a stronger association with infection-related AEs compared to other TNFi. Notably, only adalimumab shows a lower risk of viral infections, while it exhibits an increased risk of bacterial and mycobacterial infections, similar to other TNFi.
This study identified a significant association between TNFi use and infection-related AEs in pediatric patients, providing the foothold for further research. However, due to its retrospective nature, further investigations are warranted to confirm these findings and identify potential risk factors in a controlled, prospective study setting.
• There is sufficient evidence to demonstrate the infection risk associated with TNFi in adult patients. • Pediatric patients, whose immune systems are still developing, are more vulnerable to certain infections.
• There is a significant association between TNFi use and infection-related adverse events in pediatric patients, and different TNFi have distinct infection profiles.
肿瘤坏死因子抑制剂(TNFi)在儿科患者中的使用日益增加,引发了人们对其对免疫系统潜在影响及相关不良事件的担忧。TNFi引起的感染相关不良事件(AE)在现实环境中已引起广泛关注。本研究旨在全面分析和总结儿科患者中与TNFi相关的感染相关AE。进行了一项回顾性药物警戒研究,以识别2004年第一季度至2023年第一季度期间向美国食品药品监督管理局不良事件报告系统(FAERS)数据库报告的与TNFi相关感染的病例。对TNFi报告进行了仔细审查,以排除其他AE、合并用药和处方适应症等混杂因素。通过将TNFi报告与整个FAERS数据库进行比较来进行比例分析,以识别与TNFi使用显著相关的感染相关AE。在FAERS数据库中,感染相关AE占所有与TNFi相关不良事件报告的8.36%。在儿科人群中总共识别出8050例与TNFi相关的感染病例,其中2.57%的报告导致死亡。与其他TNFi相比,英夫利昔单抗和戈利木单抗与感染相关AE的关联更强。值得注意的是,只有阿达木单抗显示出较低的病毒感染风险,而与其他TNFi类似,它表现出细菌和分枝杆菌感染风险增加。
本研究确定了TNFi使用与儿科患者感染相关AE之间存在显著关联,为进一步研究提供了立足点。然而,由于其回顾性性质,有必要进行进一步调查以证实这些发现,并在对照的前瞻性研究环境中识别潜在风险因素。
• 有充分证据证明成人患者中与TNFi相关的感染风险。• 免疫系统仍在发育的儿科患者更容易受到某些感染。
• TNFi使用与儿科患者感染相关不良事件之间存在显著关联,且不同的TNFi具有不同的感染特征。