Jeyaratnam Jerold, Ter Haar Nienke M, Lachmann Helen J, Kasapcopur Ozgur, Ombrello Amanda K, Rigante Donato, Dedeoglu Fatma, Baris Ezgi H, Vastert Sebastiaan J, Wulffraat Nico M, Frenkel Joost
Department of General Pediatrics, University Medical Center Utrecht, Room KE 04 133 1, PO-Box 85090, 3508, AB Utrecht, The Netherlands.
Laboratory for Translational Immunology, University Medical Center Utrecht, Utrecht, the Netherlands.
Pediatr Rheumatol Online J. 2018 Mar 21;16(1):19. doi: 10.1186/s12969-018-0235-z.
Withholding live-attenuated vaccines in patients using interleukin (IL)-1 or IL-6 blocking agents is recommended by guidelines for both pediatric and adult rheumatic diseases, since there is a risk of infection in an immune suppressed host. However, this has never been studied. This retrospective, multicenter survey aimed to evaluate the safety of live-attenuated vaccines in patients using IL-1 or IL-6 blockade.
We contacted physicians involved in the treatment of autoinflammatory diseases to investigate potential cases. Patients were included if a live-attenuated vaccine had been administered while they were on IL-1 or IL-6 blockade.
Seventeen patients were included in this survey (7 systemic juvenile idiopathic arthritis (sJIA), 5 cryopyrin associated periodic syndrome (CAPS), 4 mevalonate kinase deficiency (MKD) and 1 familial Mediterranean fever (FMF). Three patients experienced an adverse event, of which two were serious adverse events (a varicella zoster infection after varicella zoster booster vaccination, and a pneumonia after MMR booster). One additional patient had diarrhea after oral polio vaccine. Further, seven patients experienced a flare of their disease, which were generally mild. Eight patients did not experience an adverse event or a flare.
We have described a case series of seventeen patients who received a live-attenuated vaccine while using IL-1 or IL-6 blocking medication. The findings of this survey are not a reason to adapt the existing guidelines. Prospective trials are needed in order to acquire more evidence about the safety and efficacy before considering adaptation of guidelines.
儿科和成人风湿性疾病指南均建议,在使用白细胞介素(IL)-1或IL-6阻断剂的患者中,不应接种减毒活疫苗,因为免疫抑制宿主存在感染风险。然而,此前从未对此进行过研究。这项回顾性多中心调查旨在评估在使用IL-1或IL-6阻断剂的患者中接种减毒活疫苗的安全性。
我们联系了参与自身炎症性疾病治疗的医生,以调查潜在病例。如果患者在接受IL-1或IL-6阻断治疗期间接种了减毒活疫苗,则纳入研究。
本调查共纳入17例患者(7例系统性幼年特发性关节炎(sJIA)、5例冷吡啉相关周期性综合征(CAPS)、4例甲羟戊酸激酶缺乏症(MKD)和1例家族性地中海热(FMF))。3例患者出现不良事件,其中2例为严重不良事件(水痘带状疱疹加强疫苗接种后发生水痘带状疱疹感染,麻疹腮腺炎风疹(MMR)加强疫苗接种后发生肺炎)。另有1例患者口服脊髓灰质炎疫苗后出现腹泻。此外,7例患者病情复发,一般症状较轻。8例患者未出现不良事件或病情复发。
我们描述了一个17例患者的病例系列,这些患者在使用IL-1或IL-6阻断药物的同时接种了减毒活疫苗。本次调查结果并非调整现有指南的理由。在考虑调整指南之前,需要进行前瞻性试验,以获取更多关于安全性和有效性的证据。