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造血干细胞移植作为难治性自身免疫性视网膜病变的挽救治疗:一例报告

Hematopoietic stem cell transplantation as rescue therapy for refractory autoimmune retinopathy: a case report.

作者信息

Wong Wendy Meihua, Loh Yvonne, Chan Hwei Wuen, Fong Warren, Chee Soon-Phaik, Koh Adrian, Holder Graham E

机构信息

Department of Ophthalmology, National University Hospital, National University Health System, Singapore, Singapore.

Centre for Innovation and Precision Eye Health, Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.

出版信息

Front Immunol. 2025 Jan 7;15:1484798. doi: 10.3389/fimmu.2024.1484798. eCollection 2024.

DOI:10.3389/fimmu.2024.1484798
PMID:39840055
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11747723/
Abstract

Autoimmune retinopathy (AIR) is a rare, potentially blinding retinal disease that remains a challenging condition to manage when resistant to conventional immune-modulatory approaches. We report clinical and electrophysiological improvement in a 49-year-old patient who underwent an autologous hematopoietic stem cell transplant (aHSCT) for thymoma-associated AIR after experiencing progressive disease despite receiving periocular and systemic steroids, mycophenolate mofetil, baricitinib, tacrolimus, bortezomib, rituximab, plasmapheresis, and intravenous immunoglobulin. The aHSCT had two stages: (i) peripheral blood stem cell harvest following mobilization with cyclophosphamide and granulocyte colony-stimulating factor, and (ii) conditioning regimen with plasmapheresis, rituximab, cyclophosphamide, and anti-thymocyte globulin high-dose therapy, followed by autologous hematopoietic cell infusion of 5.74 million cells. Symptoms of photopsia rapidly abated after undergoing aHSCT, and objective investigations of structure and function similarly demonstrated improvement. At 22 months' follow-up, she continued to demonstrate the durability of the clinical response. The present report suggests that in judiciously selected patients, HSCT may provide a rescue option for refractory AIR. Further cases are needed to confirm these results.

摘要

自身免疫性视网膜病(AIR)是一种罕见的、有潜在致盲风险的视网膜疾病,当对传统免疫调节方法耐药时,其治疗仍然具有挑战性。我们报告了一名49岁患者的临床和电生理改善情况,该患者因胸腺瘤相关的AIR在接受了眼周和全身类固醇、霉酚酸酯、巴瑞替尼、他克莫司、硼替佐米、利妥昔单抗、血浆置换和静脉注射免疫球蛋白治疗后病情仍进展,随后接受了自体造血干细胞移植(aHSCT)。aHSCT有两个阶段:(i)用环磷酰胺和粒细胞集落刺激因子动员后采集外周血干细胞,以及(ii)采用血浆置换、利妥昔单抗、环磷酰胺和抗胸腺细胞球蛋白大剂量疗法进行预处理方案,随后输入574万个自体造血细胞。接受aHSCT后,闪光幻觉症状迅速减轻,结构和功能的客观检查同样显示有所改善。在22个月的随访中,她继续显示出临床反应的持久性。本报告表明,在经过审慎选择的患者中,HSCT可能为难治性AIR提供一种挽救方案。需要更多病例来证实这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/b4cf61d40a84/fimmu-15-1484798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/fc55ed8fb53e/fimmu-15-1484798-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/41af8ad66fb3/fimmu-15-1484798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/ea95f3a6bb0a/fimmu-15-1484798-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/b4cf61d40a84/fimmu-15-1484798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/fc55ed8fb53e/fimmu-15-1484798-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/41af8ad66fb3/fimmu-15-1484798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/ea95f3a6bb0a/fimmu-15-1484798-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edc0/11747723/b4cf61d40a84/fimmu-15-1484798-g004.jpg

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