Department of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Pediatrics, Carmel Medical Center, Technion Faculty of Medicine, Haifa, Israel.
Department of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, the Netherlands.
Vaccine. 2023 Aug 23;41(37):5477-5482. doi: 10.1016/j.vaccine.2023.07.052. Epub 2023 Jul 27.
Vaccines, especially live attenuated vaccines, in children with JIA pose a great challenge due to both potential lower immunogenicity and safety as a result of immunosuppressive treatment. For many years, in the Netherlands, JIA patients receive a measles-mumps-rubella (MMR) booster vaccine at the age of nine years as part of the national immunization program.
To study long-term humoral immunoprotection in a large cohort of JIA patients who received the MMR booster vaccine while being treated with immunomodulatory therapies at the Wilhelmina Children's Hospital in Utrecht, the Netherlands.
MMR-specific IgG antibody concentrations in stored serum samples of vaccinated JIA patients were determined with chemiluminescent microparticle immunoassays (CMIA). Samples were analyzed five years after MMR booster vaccination and at last available follow-up visit using both crude and adjusted analyses. Additional clinical data were collected from electronic medical records.
In total, 236 samples from 182 patients were analyzed, including 67 samples that were available five years post-vaccination, and an additional 169 samples available from last visits with a median duration after vaccination of 6.9 years (IQR: 2.8-8.8). Twenty-eight patients were using biologic disease-modifying antirheumatic drugs (bDMARDS) of whom 96% anti-TNF agents and 4% tocilizumab. Percentages of protective antibody levels against measles after five years were significantly lower for patients who used bDMARD therapy at vaccination compared to patients who did not: 60% versus 86% (P = 0.03). For mumps (80% versus 94%) and rubella (60% versus 83%) this difference did not reach statistical significance (P = 0.11 and P = 0.07, respectively). Antibody levels post-vaccination decreased over time, albeit not significantly different between bDMARD users and non-bDMARD users.
The MMR booster vaccine demonstrated long-term immunogenicity in the majority of children with JIA from a large cohort, although lower percentages of protective measles antibody levels were observed in bDMARD users. Hence, it might be indicated to measure antibody levels at least five years after MMR booster vaccination in the latter group and advice an extra booster accordingly.
由于免疫抑制治疗,疫苗,尤其是减毒活疫苗,在幼年特发性关节炎(JIA)患儿中带来了巨大的挑战,因为这可能导致潜在的免疫原性降低和安全性降低。多年来,在荷兰,JIA 患者在九岁时作为国家免疫计划的一部分接受麻疹、腮腺炎和风疹(MMR)加强疫苗接种。
研究在乌得勒支威廉敏娜儿童医院接受免疫调节治疗的 JIA 患者中,接种 MMR 加强疫苗后的长期体液免疫保护作用,该研究为一项大型队列研究。
使用化学发光微粒子免疫分析(CMIA)检测接种 JIA 患者储存血清样本中的 MMR 特异性 IgG 抗体浓度。在 MMR 加强疫苗接种后五年和最后一次可获得的随访时,使用未调整和调整分析对样本进行分析。从电子病历中收集了额外的临床数据。
共分析了 182 名患者的 236 个样本,其中包括 67 个在疫苗接种后五年时可获得的样本,以及另外 169 个在最后一次随访时可获得的样本,中位随访时间为接种后 6.9 年(IQR:2.8-8.8)。28 名患者正在使用生物疾病修饰抗风湿药物(bDMARD),其中 96%为抗 TNF 制剂,4%为托珠单抗。与未使用 bDMARD 治疗的患者相比,在接种疫苗时使用 bDMARD 治疗的患者五年后针对麻疹的保护性抗体水平显著较低:60%对 86%(P=0.03)。对于腮腺炎(80%对 94%)和风疹(60%对 83%),这种差异无统计学意义(P=0.11 和 P=0.07)。接种疫苗后,抗体水平随时间下降,但 bDMARD 使用者和非 bDMARD 使用者之间没有显著差异。
MMR 加强疫苗在来自大型队列的大多数 JIA 儿童中表现出长期的免疫原性,尽管 bDMARD 使用者的保护性麻疹抗体水平百分比较低。因此,在后者中,至少在 MMR 加强疫苗接种五年后测量抗体水平并相应地建议额外加强疫苗接种可能是必要的。