首页> 外文期刊>Pediatric rheumatology online journal >Scoping review of biological treatment of deficiency of interleukin-36 receptor antagonist (DITRA) in children and adolescents
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Scoping review of biological treatment of deficiency of interleukin-36 receptor antagonist (DITRA) in children and adolescents

机译:儿童和青少年白细胞介素-36受体拮抗剂(DITRA)缺乏的生物学治疗综述

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Deficiency of interleukin-36 receptor antagonist (DITRA) is a life threatening monogenic autoinflammatory disease caused by loss of function mutations in the IL36RN gene. Affected patients develop recurrent episodes of generalized pustular psoriasis (GPP) with systemic inflammation and fever. We here review and analyze the literature on pediatric DITRA patients who have been treated by biologicals targeting inflammatory cytokines. A database research was performed to identify all relevant articles on pediatric DITRA patients treated with biologicals. According to defined response criteria therapeutic efficacy was analyzed. Our literature research revealed 12 pediatric patients with DITRA who have received treatment with biologicals and we add a further not yet reported patient. Out of these 13 patients 10 were homozygous including 6 with the p.Leu27Pro, 3 with the p.Arg10 Argfs* and 1 with the p.Thr123Met mutation. 3 patients were compound heterozygous. In total 28 flares were treated with biological agents- targeting IL-1, IL-17, IL-12/23 and TNF-α. Complete response was achieved in 16 flares (57%), a partial reponse was seen in 2 flares (7%), and no response was observed in 10 flares (36%). Response rates were heterogeneous among the different agents. While complete/partial/no response with inhibition of TNF-alpha could be achieved in 7 (58%)/1 (8%)/4 (33%), the inhibition of IL-17 and of IL-12/23 led in each 4 flares to a 100% complete response. IL-1 inhibition led to complete/partial response in each 1 (13%) and was not effective in 6 (76%) flares. Of note, the novel patient was successfully treated with weekly dosed adalimumab. DITRA is a rare disease that has to be considered in GPP with systemic inflammation and fever. It can be effectively treated with specific biological inhibition of TNF-alpha, IL-12/23 and IL- 17, while anti-IL-1 treatment seems less effective. Weekly dosed adalimumab appears to be a treatment option for pediatric patients. Further reports and studies of biological treated pediatric DITRA patients are warranted for evaluation of optimal treatment.
机译:白细胞介素-36受体拮抗剂(DITRA)的缺乏是威胁危及IL36RN基因中功能突变损失引起的单一的自身炎性疾病。受影响的患者用全身炎症和发烧开发出普遍的脓疱性牛皮癣(GPP)的复发性发作。我们在这里审查并分析了由靶向炎症细胞因子的生物学治疗的儿科DITRA患者的文献。进行了数据库研究,以鉴定用生物学治疗的儿科DITRA患者的所有相关文章。根据定义的响应标准分析治疗疗效。我们的文献研究揭示了12名儿科患者患有生物学治疗的DITRA,我们添加了另一种尚未报道的患者。在这13名患者中,10例纯合,其中P.LEU27PRO,3,具有P.ARG10 ARGFS *和1,具有P.Thrl123met突变。 3名患者是复合的杂合。总共28张耀斑用生物制剂 - 靶向IL-1,IL-17,IL-12/23和TNF-α处理。在16张耀斑(57%)中实现了完全响应,在2张耀斑(7%)中看到了一部分响应,并且在10张耀斑中没有观察到响应(36%)。不同剂量的反应率是异质的。在7(58%)/ 1(8%)/ 4(33%)中可以实现完全/部分/无抑制TNF-α的反应,而IL-17和IL-12/23 LED的抑制作用每4兆均为100%完全响应。 IL-1抑制导致每1(13%)的完全/部分反应,在6(76%)耀斑中无效。值得注意的是,新型患者用每周剂量的Adalimumab成功治疗。 DITRA是一种罕见的疾病,必须以全身的炎症和发烧在GPP中考虑。可以有效地用TNF-α,IL-12/23和IL-17的特异性生物学抑制治疗,而抗IL-1治疗似乎效果较差。每周给药的达铝算命象似乎是儿科患者的治疗选择。有必要进一步报告和研究生物处理的儿科DITRA患者进行最佳治疗评估。

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