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儿童异基因造血干细胞移植后自身免疫性血细胞减少症的危险因素、治疗和免疫失调。

Risk Factors, Treatment, and Immune Dysregulation in Autoimmune Cytopenia after Allogeneic Hematopoietic Stem Cell Transplantation in Pediatric Patients.

机构信息

Department of Pediatrics, Section Immunology, Hematology and Stem Cell Transplantation, Leiden University Medical Center, Leiden, The Netherlands.

Department of Pediatrics, Laboratory for Immunology, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Biol Blood Marrow Transplant. 2018 Apr;24(4):772-778. doi: 10.1016/j.bbmt.2017.12.782. Epub 2017 Dec 19.

Abstract

Autoimmune or alloimmune cytopenia (AIC) is a known rare complication of hematopoietic stem cell transplantation (SCT). AIC after SCT is considered difficult to treat and is associated with high morbidity and mortality. In this retrospective study in pediatric patients we evaluated incidence, outcome, potential risk factors, and current treatment strategies. A nested matched case-control study was performed to search for biomarkers associated with AIC. Of 531 consecutive SCTs at our center between 2000 and 2016, 26 were complicated by the development of AIC (cumulative incidence, 5.0%) after a median of 5 months post-SCT. Autoimmune hemolytic anemia was the most common AIC with 12 patients (46%). We identified nonmalignant disease, alemtuzumab serotherapy pre-SCT, and cytomegalovirus (CMV) reactivation as independently associated risk factors. The cytokine profile of patients at the time of AIC diagnosis appeared to skew toward a more pronounced Th 2 response compared with control subjects at the corresponding time point post-SCT. Corticosteroids and intravenous immunoglobulin as first-line treatment or a wait-and-see approach led to resolution of AIC in 35% of cases. Addition of step-up therapies rituximab (n = 15), bortezomib (n = 7), or sirolimus (n = 3) was associated with AIC resolution in 40%, 57%, and 100% of cases, respectively. In summary, we identified CMV reactivation post-SCT as a new clinical risk factor for the development of AIC in children. The cytokine profile during AIC appears to favor a Th 2 response. Rituximab, bortezomib, and sirolimus are promising step-up treatment modalities.

摘要

自身免疫或同种免疫血细胞减少症(AIC)是造血干细胞移植(SCT)后已知的罕见并发症。SCT 后 AIC 被认为难以治疗,且与高发病率和死亡率相关。在这项儿科患者的回顾性研究中,我们评估了发病率、结局、潜在风险因素和当前的治疗策略。为了寻找与 AIC 相关的生物标志物,我们进行了一项嵌套匹配病例对照研究。在我们中心,2000 年至 2016 年期间进行了 531 例连续 SCT,其中 26 例在 SCT 后中位数为 5 个月后发生 AIC(累积发生率为 5.0%)。自身免疫性溶血性贫血是最常见的 AIC,有 12 例(46%)。我们确定了非恶性疾病、SCT 前阿仑单抗血清疗法和巨细胞病毒(CMV)再激活作为独立相关的危险因素。与 SCT 后相应时间点的对照相比,AIC 诊断时患者的细胞因子谱似乎偏向于更明显的 Th2 反应。皮质类固醇和静脉注射免疫球蛋白作为一线治疗或观望方法使 35%的 AIC 得到缓解。添加升级治疗利妥昔单抗(n=15)、硼替佐米(n=7)或西罗莫司(n=3)分别使 40%、57%和 100%的病例 AIC 得到缓解。总之,我们发现 SCT 后 CMV 再激活是儿童发生 AIC 的新临床危险因素。AIC 期间的细胞因子谱似乎有利于 Th2 反应。利妥昔单抗、硼替佐米和西罗莫司是很有前途的升级治疗方法。

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