Advancing autoimmune Rheumatic disease treatment: CAR-T Cell Therapies - Evidence, Safety, and future directions

被引:7
|
作者
Ohno, Ryunosuke [1 ,2 ]
Nakamura, Akihiro [1 ,3 ,4 ,5 ]
机构
[1] Queens Univ, Dept Med, Div Rheumatol, 94 Stuart St, Kingston, ON K7L 3N6, Canada
[2] Okayama Univ, Dept Med, Okayama, Japan
[3] Queens Univ, Translat Inst Med, Sch Med, Kingston, ON, Canada
[4] Kingston Hlth Sci Ctr, Rheumatol Clin, Kingston, ON, Canada
[5] Queens Univ, Translat Inst Med, Sch Med, Dept Med, 94 Stuart St, Kingston, ON K7L 3N6, Canada
关键词
Anti-neutrophil cytoplasmic autoantibody; (ANCA)-associated vasculitis (AAV); Antisynthetase syndrome (ASS); Autoimmune rheumatic diseases (ARDs); Chimeric Antigen Receptor (CAR)-T Cell; Chimeric autoantibody receptor T (CAAR-T) cells; Cytokine release syndrome (CRS); Immune effector cell associated neurotoxicity; syndrome (ICANS); cells; Regulatory T cells (Treg) expressing CAR (CAR-Tregs); Systemic lupus erythematosus (SLE); Systemic sclerosis (SSc); SYSTEMIC-LUPUS-ERYTHEMATOSUS; B-CELLS; DOUBLE-BLIND; RITUXIMAB; ARTHRITIS; EFFICACY; SCLEROSIS; CYCLOPHOSPHAMIDE; MULTICENTER; CHALLENGES;
D O I
10.1016/j.semarthrit.2024.152479
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Despite advancements in managing autoimmune rheumatic diseases (ARDs) with existing treatments, many patients still encounter challenges such as inadequate responses, difficulty in maintaining remission, and side effects. Chimeric Antigen Receptor (CAR) T-cell therapy, originally developed for cancer, has now emerged as a promising option for cases of refractory ARDs. Methods: A search of the literature was conducted to compose a narrative review exploring the current evidence, potential safety, limitations, potential modifications, and future directions of CAR-T cells in ARDs. Results: CAR-T cell therapy has been administered to patients with refractory ARDs, including systemic lupus erythematosus, antisynthetase syndrome, and systemic sclerosis, demonstrating significant improvement. Notable responses include enhanced clinical symptoms, reduced serum autoantibody titers, and sustained remissions in disease activity. Preclinical and in vitro studies using both animal and human samples also support the efficacy and elaborate on potential mechanisms of CAR-T cells against antineutrophil cytoplasmic antibodyassociated vasculitis and rheumatoid arthritis. While cautious monitoring of adverse events, such as cytokine release syndrome, is crucial, the therapy appears to be highly tolerable. Nevertheless, challenges persist, including cost, durability due to potential CAR-T cell exhaustion, and manufacturing complexities, urging the development of innovative solutions to further enhance CAR-T cell therapy accessibility in ARDs. Conclusions: CAR-T cell therapy for refractory ARDs has demonstrated high effectiveness. While no significant warning signs are currently reported, achieving a balance between therapeutic efficacy and safety is vital in adapting CAR-T cell therapy for ARDs. Moreover, there is significant potential for technological advancements to enhance the delivery of this treatment to patients, thereby ensuring safer and more effective disease control for patients.
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页数:10
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