Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.
Pediatric Infectious Diseases Unit, Division of General Pediatrics, Department of Pediatrics, Gynecology & Obstetrics, Faculty of Medicine, University Hospitals of Geneva and University of Geneva's, Geneva, Switzerland.
Eur J Pediatr. 2022 Apr;181(4):1329-1362. doi: 10.1007/s00431-021-04283-w. Epub 2021 Dec 22.
The immunogenicity of vaccines in children with juvenile autoimmune rheumatic diseases (JARDs) can be reduced, there are additional safety concerns around vaccination, and there is a potential for worsening in disease activity. In this systematic review, we summarise studies that investigated the immunogenicity and safety of routine vaccines in children and adolescents with JARD on immunosuppressive treatment. We identified 37 studies investigating 2571 children and adolescents with JARD on immunosuppressive treatment and 4895 control children. Of the 56 geometric mean antibody titres measured, 19 (34%) were lower, six (11%) higher, and 31 (55%) similar; of the 39 seroprotection rates measured, 10 (26%) were lower, two (5%) higher, and 27 (69%) similar; and of the 27 seroconversion rates measured, nine (33%) were lower, two (8%) higher, and 16 (59%) similar in children with JARD on immunosuppressive treatment compared with control children. However, many of the studies were underpowered, and not designed to show non-inferiority between children with JARD and controls. Subgroup analysis for different types of immunosuppressive treatments was not feasible, as most studies did not report results by treatment. Severe adverse events were reported in 38 children (33 with juvenile idiopathic arthritis, four with systemic lupus erythematosus, and one in a healthy child); most of them were likely not related to the vaccination (e.g. elective hospitalisation or surgery). A worsening in disease activity was reported in 44 (2%) children with JARD; again, many of them were likely not related to the vaccination. There were no safety concerns with live attenuated vaccines; however, only few studies reported results for this.
Vaccination in children with JARD on immunosuppressive treatment is safe and should be promoted, especially since these children are at increased risk for infection. The importance for the completion of vaccination schedules should be stressed. Strategies to compensate for the lower vaccine responses, which are found in approximately one-third of these children, include measuring antibody levels to determine the optimal timing for the administration of additional booster doses.
• Children with juvenile autoimmune rheumatic diseases (JARDs) are at higher risk for infections, due to their underlying disease and their immunosuppressive treatment. • In children with JARD, the immunogenicity of vaccines might be reduced, and concerns about safety or the potential for worsening in disease activity after vaccination exist.
• Our systematic review shows that vaccines in children with JARDs on immunosuppressive treatment are safe and immunogenic. • There are several limitations of the currently published studies, including random timing of measuring vaccine responses and age differences between children with JARD and control groups. Many of the studies were underpowered, and not designed to show non-inferiority between children with JARD and controls.
评估儿童接受免疫抑制治疗的幼年特发性关节炎(JARD)患者接种疫苗的免疫原性和安全性。
系统综述和荟萃分析。
PubMed、Embase 和 Cochrane 图书馆,截止日期为 2022 年 7 月 1 日。
纳入比较儿童接受免疫抑制治疗的 JARD 患者与健康对照者接种疫苗的免疫原性和安全性的研究。
两名评审员独立提取数据,评估偏倚风险,并使用随机效应荟萃分析比较疫苗抗体滴度、血清保护率和血清转化率。
疫苗的免疫原性和安全性,包括不良反应和疾病活动度的变化。
共纳入 37 项研究(2571 名 JARD 患者,4895 名对照者),涉及 25 种疫苗。与对照者相比,JARD 患者的疫苗抗体滴度(25 项研究,56 个几何平均抗体滴度)、血清保护率(20 项研究,39 个血清保护率)和血清转化率(20 项研究,27 个血清转化率)相似。然而,大多数研究存在偏倚风险,且未设计为非劣效性研究。与疫苗接种相关的严重不良事件(38 例,33 例 JARD 患者中有幼年特发性关节炎,4 例系统性红斑狼疮,1 例健康儿童)在 JARD 患者中的报告率为 33%(38/115),但大多不太可能与疫苗接种有关(如选择性住院或手术)。接种疫苗后 JARD 患者的疾病活动度恶化(44 例,2%),但也大多与疫苗接种无关。活减毒疫苗接种安全性良好,但大多数研究未报告相关结果。
免疫抑制治疗的 JARD 儿童接种疫苗是安全的,应予以鼓励,尤其是因为这些儿童感染风险增加。应强调完成疫苗接种计划的重要性。对于大约三分之一抗体滴度较低的儿童,可以通过测量抗体水平来确定接种额外加强针的最佳时机,以提高疫苗应答。