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Front Immunol. 2023 Jun 7;14:1128581. doi: 10.3389/fimmu.2023.1128581. eCollection 2023.
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Lentiviral gene therapy for X-linked chronic granulomatous disease recapitulates endogenous CYBB regulation and expression.慢病毒基因治疗 X 连锁慢性肉芽肿病再现内源性 CYBB 调控和表达。
Blood. 2023 Mar 2;141(9):1007-1022. doi: 10.1182/blood.2022016074.
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Hematopoietic Stem Cell Transplantation in Late-onset X-linked Chronic Granulomatous Disease in a Female Carrier.女性携带者迟发性X连锁慢性肉芽肿病的造血干细胞移植
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女性 X 连锁慢性肉芽肿病携带者的异基因 HSCT。

Allogeneic HSCT for Symptomatic Female X-linked Chronic Granulomatous Disease Carriers.

机构信息

Paediatric Haematopoietic Stem Cell Transplant Unit, Great North Children's Hospital, Ward 3, Newcastle Upon Tyne, NE1 4LP, UK.

Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.

出版信息

J Clin Immunol. 2023 Nov;43(8):1964-1973. doi: 10.1007/s10875-023-01570-z. Epub 2023 Aug 24.

DOI:10.1007/s10875-023-01570-z
PMID:37620741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10661721/
Abstract

X-linked chronic granulomatous disease (XL-CGD) is an inherited disorder of superoxide production, causing failure to generate the oxidative burst in phagocytes. It is characterized by invasive bacterial and fungal infections, inflammation, and chronic autoimmune disease. While XL-CGD carriers were previously assumed to be healthy, a range of clinical manifestations with significant morbidity have recently been described in a subgroup of carriers with impaired neutrophil oxidative burst due to skewed lyonization. Allogeneic hematopoietic stem cell transplantation (HSCT) is the standard curative treatment for CGD but has rarely been reported in individual symptomatic carriers to date. We undertook a retrospective international survey of outcome of HSCT for symptomatic XL-CGD carriers. Seven symptomatic female XL-CGD carriers aged 1-56 years underwent HSCT in four centers, indicated for severe and recurrent infection, colitis, and autoimmunity. Two patients died from transplant-related complications, following donor engraftment and restoration of oxidative burst. All surviving patients demonstrated resolution of their neutrophil oxidative burst defect with concordant reduction in infection and inflammatory symptoms and freedom from further immunosuppressive therapy. In conclusion, allogeneic HSCT may cure the phagocyte defect in symptomatic XL-CGD carriers and improve their recurrent and disabling infective and inflammatory symptoms but risks transplant-related complications.

摘要

X 连锁慢性肉芽肿病(XL-CGD)是一种超氧化物产生的遗传性疾病,导致吞噬细胞无法产生氧化爆发。它的特征是侵袭性细菌和真菌感染、炎症和慢性自身免疫性疾病。虽然以前认为 XL-CGD 携带者是健康的,但由于 Lyonization 偏斜导致中性粒细胞氧化爆发受损,最近在一组携带者中描述了一系列具有显著发病率的临床表现。异基因造血干细胞移植(HSCT)是 CGD 的标准治愈治疗方法,但迄今为止,在个别有症状的携带者中很少有报道。我们对有症状的 XL-CGD 携带者进行了 HSCT 结果的回顾性国际调查。四名中心的 7 名年龄为 1-56 岁的有症状的女性 XL-CGD 携带者因严重和复发性感染、结肠炎和自身免疫而接受了 HSCT。两名患者在供体植入和氧化爆发恢复后死于移植相关并发症。所有存活的患者均表现出中性粒细胞氧化爆发缺陷的解决,同时感染和炎症症状也相应减少,且无需进一步免疫抑制治疗。总之,异基因 HSCT 可能治愈有症状的 XL-CGD 携带者的吞噬细胞缺陷,并改善其复发性和致残性感染和炎症症状,但存在移植相关并发症的风险。