Department of Medicine, Division of Allergy/Immunology, Washington University in St. Louis, St. Louis, MO, United States.
Department of Pediatrics, Division of Gastroenterology/Nutrition, Washington University in St. Louis, St. Louis, MO, United States.
Front Immunol. 2022 Apr 5;13:863218. doi: 10.3389/fimmu.2022.863218. eCollection 2022.
Disorders of immune dysregulation following heart transplantation in children have been reported; however, the management of such disorders remains uncertain and challenging. In this case report, we describe a clinical course of a child with severe autoimmune enteropathy after a heart transplant in infancy and detail a treatment approach with abatacept and alemtuzumab. A 21-month-old girl with a medical history of congenital dilated cardiomyopathy and heart transplantation at 2 months was evaluated for chronic hematochezia. The patient underwent an extensive workup, including endoscopic biopsy which showed crypt apoptosis, similar to that seen with graft-versus-host disease (GVHD). Results of her immune workup were consistent with status post-thymectomy but also demonstrated evidence of immune dysregulation. Specifically, her immune phenotype at diagnosis demonstrated T-cell lymphopenia, restricted TCR repertoire and skewing of T-cell compartment toward memory phenotype, increase in serum soluble ILR2a, and hypergammaglobulinemia. In the absence of response to more standard immune modulation, the patient was treated with CTLA4-Ig (abatacept), followed by a combination of abatacept and a JAK inhibitor and, finally, a combination of abatacept and alemtuzumab. Following therapy with alemtuzumab, the patient achieved remission for the first time in her life. Her clinical course was complicated by a relapse after 6 months which again readily responded to alemtuzumab. Ultimately, despite these remissions, the patient suffered an additional relapse. This case highlights the challenges of neonatal thymectomy and adds new insights into the pathogenesis, diagnosis, and management of severe autoimmune enteropathy in pediatric heart transplant recipients.
儿童心脏移植后免疫失调紊乱已有报道;然而,此类疾病的治疗仍存在不确定性和挑战性。在本病例报告中,我们描述了一例婴儿期心脏移植后发生严重自身免疫性肠炎的患儿的临床经过,并详细介绍了使用阿巴西普和阿仑单抗的治疗方法。
一名 21 个月大的女孩,患有先天性扩张型心肌病,2 个月大时接受心脏移植,因慢性血便就诊。患者接受了广泛的检查,包括内镜活检,结果显示隐窝凋亡,类似于移植物抗宿主病(GVHD)。她的免疫检查结果与胸腺切除术后相符,但也显示出免疫失调的证据。具体来说,她在诊断时的免疫表型表现为 T 细胞淋巴细胞减少症、TCR 受体受限和 T 细胞亚群向记忆表型偏向、血清可溶性 ILR2a 增加以及高丙种球蛋白血症。由于对更标准的免疫调节治疗无反应,患者接受 CTLA4-Ig(阿巴西普)治疗,随后联合使用阿巴西普和 JAK 抑制剂,最后联合使用阿巴西普和阿仑单抗。使用阿仑单抗治疗后,患者一生中首次获得缓解。她的临床过程在 6 个月时出现复发,再次容易对阿仑单抗产生反应。最终,尽管这些缓解发生,患者仍出现了另外一次复发。
该病例突出了新生儿胸腺切除术的挑战,并为儿科心脏移植受者严重自身免疫性肠炎的发病机制、诊断和治疗提供了新的见解。