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CD40 配体缺陷的造血干细胞移植:来自 EBMT/ESID-IEWP-SCETIDE-PIDTC 研究的结果。

Hematopoietic stem cell transplantation for CD40 ligand deficiency: Results from an EBMT/ESID-IEWP-SCETIDE-PIDTC study.

机构信息

Department of Pediatric Immunology and HSCT, Great North Children's Hospital, Newcastle upon Tyne, United Kingdom; San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Pediatric Immunohematology and Bone Marrow Transplantation Unit, San Raffaele Scientific Institute, Milan, Italy; Vita-Salute San Raffaele University, Milan, Italy.

Center of Biostatistics for Clinical Epidemiology, School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

出版信息

J Allergy Clin Immunol. 2019 Jun;143(6):2238-2253. doi: 10.1016/j.jaci.2018.12.1010. Epub 2019 Jan 17.

Abstract

BACKGROUND

CD40 ligand (CD40L) deficiency, an X-linked primary immunodeficiency, causes recurrent sinopulmonary, Pneumocystis and Cryptosporidium species infections. Long-term survival with supportive therapy is poor. Currently, the only curative treatment is hematopoietic stem cell transplantation (HSCT).

OBJECTIVE

We performed an international collaborative study to improve patients' management, aiming to individualize risk factors and determine optimal HSCT characteristics.

METHODS

We retrospectively collected data on 130 patients who underwent HSCT for CD40L deficiency between 1993-2015. We analyzed outcome and variables' relevance with respect to survival and cure.

RESULTS

Overall survival (OS), event-free survival (EFS), and disease-free survival (DFS) were 78.2%, 58.1%, and 72.3% 5 years after HSCT. Results were better in transplantations performed in 2000 or later and in children less than 10 years old at the time of HSCT. Pre-existing organ damage negatively influenced outcome. Sclerosing cholangitis was the most important risk factor. After 2000, superior OS was achieved with matched donors. Use of myeloablative regimens and HSCT at 2 years or less from diagnosis associated with higher OS and DFS. EFS was best with matched sibling donors, myeloablative conditioning (MAC), and bone marrow-derived stem cells. Most rejections occurred after reduced-intensity or nonmyeloablative conditioning, which associated with poor donor cell engraftment. Mortality occurred mainly early after HSCT, predominantly from infections. Among survivors who ceased immunoglobulin replacement, T-lymphocyte chimerism was 50% or greater donor in 85.2%.

CONCLUSION

HSCT is curative in patients with CD40L deficiency, with improved outcome if performed before organ damage development. MAC is associated with better OS, EFS, and DFS. Prospective studies are required to compare the risks of HSCT with those of lifelong supportive therapy.

摘要

背景

CD40 配体(CD40L)缺乏症是一种 X 连锁的原发性免疫缺陷病,会导致反复发作的肺、肺囊虫和隐孢子虫感染。采用支持性治疗,长期生存预后较差。目前,唯一的根治性治疗方法是造血干细胞移植(HSCT)。

目的

我们进行了一项国际协作研究,旨在改善患者的管理,确定个体化的危险因素,并确定 HSCT 的最佳特征。

方法

我们回顾性地收集了 1993 年至 2015 年间 130 例接受 CD40L 缺乏症 HSCT 的患者数据。我们分析了与生存和治愈相关的结果和变量的相关性。

结果

HSCT 后 5 年的总生存率(OS)、无事件生存率(EFS)和无疾病生存率(DFS)分别为 78.2%、58.1%和 72.3%。2000 年或以后进行的移植和 HSCT 时年龄小于 10 岁的患者结果更好。预先存在的器官损伤对结果有负面影响。硬化性胆管炎是最重要的危险因素。2000 年后,与匹配供体相比,OS 更高。采用清髓性方案和诊断后 2 年内进行 HSCT 与更高的 OS 和 DFS 相关。EFS 最好的是匹配的同胞供体、清髓性预处理(MAC)和骨髓来源的干细胞。大多数排斥反应发生在减强度或非清髓性预处理后,与供体细胞植入不良相关。死亡主要发生在 HSCT 后早期,主要是感染引起的。在停止免疫球蛋白替代治疗的幸存者中,85.2%的患者 T 淋巴细胞嵌合率为 50%或更高。

结论

HSCT 可治愈 CD40L 缺乏症患者,如果在器官损伤发生前进行,则预后更好。MAC 与更好的 OS、EFS 和 DFS 相关。需要前瞻性研究来比较 HSCT 的风险与终身支持性治疗的风险。

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