CD19-Directed CAR T-Cells in a Patient With Refractory MOGAD: Clinical and Immunologic Follow-Up for 1 Year.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Jose Maria Cabrera-Maqueda, Maria Sepulveda, Raquel Ruiz García, Guillermo Muñoz-Sánchez, Nuria Martínez-Cibrian, Valentín Ortíz-Maldonado, Daniel Lorca-Arce, Mar Guasp, Sara Llufriu, Eugenia Martinez-Hernandez, Thais Armangue, Elianet G Fonseca, María Teresa Alba-Isasi, Julio Delgado, Josep Dalmau, Manel Juan, Albert Saiz, Yolanda Blanco
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引用次数: 0

Abstract

Objectives: In MOG antibody-associated disease (MOGAD), relapse prevention and the treatment approach to refractory symptoms are unknown. We report a patient with refractory MOGAD treated with CD19-directed CAR T-cells.

Methods: CD19-directed CAR T-cells (ARI-0001) were produced in-house by lentiviral transduction of autologous fresh leukapheresis and infused after a conventional lymphodepleting regimen.

Results: A 18-year-old man developed 2 episodes of myelitis associated with serum MOG-IgG, which were followed by 6 episodes of left optic neuritis (ON) and sustained the presence of MOG-IgG over 6 years despite multiple immunotherapies. After the sixth episode of ON, accompanied by severe residual visual deficits, CAR T-cell treatment was provided without complications. Follow-up of cell counts showed complete depletion of CD19+ B cells at day +7; reconstituted B cells at day +141 showing a naïve B-cell phenotype, and low or absent memory B cells and plasmablasts for 1 year. MOG-IgG titers have remained undetectable since CAR T-cell infusion. The patient had an early episode of left ON at day +29, when MOG-IgG was already negative, and since then he has remained free of relapses without immunotherapy for 1 year.

Discussion: This clinical case shows that CD19-directed CAR T-cell therapy is well-tolerated and is a potential treatment for patients with refractory MOGAD.

Classification of evidence: This provides Class IV evidence. It is a single observational study without controls.

CD19 导向 CAR T 细胞治疗难治性 MOGAD 患者:临床和免疫学随访 1 年。
目的:对于 MOG 抗体相关疾病(MOGAD),预防复发和治疗难治性症状的方法尚不清楚。我们报告了一名接受 CD19 导向 CAR T 细胞治疗的难治性 MOGAD 患者:CD19定向CAR T细胞(ARI-0001)是通过慢病毒转导自体新鲜白细胞产生的,并在常规淋巴清除疗法后输注:一名 18 岁的男子两次患上脊髓炎并伴有血清 MOG-IgG,之后又患上 6 次左侧视神经炎(ON),尽管接受了多种免疫疗法,但 MOG-IgG 的存在持续了 6 年之久。在第六次视神经炎发作并伴有严重的残余视力障碍后,患者接受了CAR T细胞治疗,未出现并发症。细胞计数随访显示,CD19+ B细胞在+7天时完全耗竭;+141天时重组的B细胞显示出幼稚B细胞表型,1年内记忆B细胞和浆细胞数量较少或消失。自 CAR T 细胞输注后,MOG-IgG 滴度一直未检测到。患者在第 +29 天早期出现左侧ON,当时MOG-IgG已呈阴性,此后1年未接受免疫治疗,一直未复发:本临床病例表明,CD19导向的CAR T细胞疗法耐受性良好,是难治性MOGAD患者的一种潜在治疗方法:本研究提供了IV级证据。这是一项没有对照的单项观察性研究。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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