Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, Albert Ludwig University of Freiburg, Freiburg, Germany.
Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center, Faculty of Medicine, Albert Ludwig University of Freiburg, Freiburg, Germany; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center, Faculty of Medicine, Albert Ludwig University of Freiburg, Freiburg, Germany.
J Allergy Clin Immunol. 2022 Feb;149(2):736-746. doi: 10.1016/j.jaci.2021.04.039. Epub 2021 Jun 7.
Heterozygous germline mutations in cytotoxic T lymphocyte-associated antigen-4 (CTLA4) impair the immunomodulatory function of regulatory T cells. Affected individuals are prone to life-threatening autoimmune and lymphoproliferative complications. A number of therapeutic options are currently being used with variable effectiveness.
Our aim was to characterize the responsiveness of patients with CTLA-4 insufficiency to specific therapies and provide recommendations for the diagnostic workup and therapy at an organ-specific level.
Clinical features, laboratory findings, and response to treatment were reviewed retrospectively in an international cohort of 173 carriers of CTLA4 mutation. Patients were followed between 2014 and 2020 for a total of 2624 months from diagnosis. Clinical manifestations were grouped on the basis of organ-specific involvement. Medication use and response were recorded and evaluated.
Among the 173 CTLA4 mutation carriers, 123 (71%) had been treated for immune complications. Abatacept, rituximab, sirolimus, and corticosteroids ameliorated disease severity, especially in cases of cytopenias and lymphocytic organ infiltration of the gut, lungs, and central nervous system. Immunoglobulin replacement was effective in prevention of infection. Only 4 of 16 patients (25%) with cytopenia who underwent splenectomy had a sustained clinical response. Cure was achieved with stem cell transplantation in 13 of 18 patients (72%). As a result of the aforementioned methods, organ-specific treatment pathways were developed.
Systemic immunosuppressants and abatacept may provide partial control but require ongoing administration. Allogeneic hematopoietic stem cell transplantation offers a possible cure for patients with CTLA-4 insufficiency.
细胞毒性 T 淋巴细胞相关抗原 4(CTLA4)的种系杂合突变会损害调节性 T 细胞的免疫调节功能。受影响的个体易发生危及生命的自身免疫和淋巴增生性并发症。目前正在使用多种治疗方法,但疗效各不相同。
我们旨在描述 CTLA-4 功能不全患者对特定治疗的反应,并提供在器官特异性水平进行诊断和治疗的建议。
我们回顾性分析了 173 名 CTLA4 突变携带者的国际队列的临床特征、实验室检查结果和治疗反应。患者在 2014 年至 2020 年期间共随访 2624 个月,从诊断开始。根据器官特异性受累情况对临床表现进行分组。记录和评估药物使用和反应。
在 173 名 CTLA4 突变携带者中,有 123 名(71%)因免疫并发症接受了治疗。阿巴西普、利妥昔单抗、西罗莫司和皮质类固醇改善了疾病严重程度,尤其是在出现血细胞减少和胃肠道、肺部和中枢神经系统的淋巴细胞器官浸润的情况下。免疫球蛋白替代治疗可有效预防感染。在 16 名血细胞减少症患者中,仅 4 名(25%)接受脾切除术的患者有持续的临床反应。18 名患者中有 13 名(72%)接受造血干细胞移植后痊愈。由于采用了上述方法,制定了器官特异性治疗途径。
全身性免疫抑制剂和阿巴西普可能提供部分控制,但需要持续给药。异基因造血干细胞移植可为 CTLA-4 功能不全患者提供可能的治愈方法。