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首页> 外文期刊>European journal of pediatrics >Variable outcome of experimental interferon-gamma therapy of disseminated Bacillus Calmette-Guerin infection in two unrelated interleukin-12Rbeta1-deficient Slovakian children.
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Variable outcome of experimental interferon-gamma therapy of disseminated Bacillus Calmette-Guerin infection in two unrelated interleukin-12Rbeta1-deficient Slovakian children.

机译:在两个无关的白细胞介素12Rbeta1缺陷的斯洛伐克儿童中,传播的卡介苗-Guerin芽孢杆菌感染的实验性干扰素-γ治疗的可变结果。

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Mycobacterium bovis Bacillus Calmette-Guerin (BCG) is an attenuated live vaccine that may cause life-threatening clinical disease in children with impaired immunity. In particular, patients with any of the nine known inherited disorders of the interleukin-12/23 interferon-gamma (IL-12/23-IFNgamma) axis are highly vulnerable to BCG. We describe two unrelated young Slovakian children suffering from disseminated BCG infection which developed shortly after routine BCG vaccination after birth. During treatment with selected anti-BCG antibiotics, resistance against several of these drugs developed. In both children, interleukin-12/23 receptor beta1 (IL-12/23Rbeta1) deficiency was diagnosed. Thus, in addition to chemotherapy, immunomodulatory treatment with recombinant IFN-gamma was performed as the pathogenesis of BCG disease in IL-12Rbeta1 deficiency involves impaired IL-12- and IL-23-dependent IFN-gamma production by lymphocytes. One child responded to treatment and is presently doing well whereas the second patient died. Conclusion:The marked variability of outcome of disseminated Bacillus Calmette-Guerin disease in interleukin-12/23 receptor beta1-deficient children sharing the same ethnic origin and exposed to a similar environment as presented in these case reports has to be taken into consideration for diagnosis and treatment of infections due to this genetic defect.
机译:牛分枝杆菌卡介苗(BCG)是一种减毒活疫苗,可能会导致免疫力低下的儿童危及生命的临床疾病。特别地,患有白介素12/23干扰素-γ(IL-12 /23-IFNγ)轴的九种已知遗传性疾病中的任何一种的患者极易受到BCG的伤害。我们描述了两个散布的BCG感染的斯洛伐克幼小儿童,这些儿童在出生后常规BCG疫苗接种后不久就发展起来。在使用选定的抗BCG抗生素治疗期间,对其中几种药物产生了耐药性。在这两个孩子中,均诊断出白细胞介素12/23受体beta1(IL-12 / 23Rbeta1)缺乏。因此,除了化学疗法之外,还进行了重组IFN-γ的免疫调节治疗,因为IL-12Rbeta1缺乏的BCG疾病的发病机制涉及淋巴细胞受损的IL-12和IL-23依赖性IFN-γ产生。一个孩子对治疗有反应,目前状况良好,而第二个病人死亡。结论:与这些病例报告相同的具有相同血统的白细胞介素-12/23受体β1缺陷型儿童中传播的卡介苗-瓜林芽孢杆菌病结局的显着变异性必须予以考虑,以进行诊断以及由这种遗传缺陷引起的感染的治疗。

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