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CD19:系统性硬化症的一个有前途的靶点。

CD19: a promising target for systemic sclerosis.

机构信息

Department of Dermatology, Kanazawa Red Cross Hospital, Japanese Red Cross Society, Kanazawa, Ishikawa, Japan.

出版信息

Front Immunol. 2024 Oct 3;15:1454913. doi: 10.3389/fimmu.2024.1454913. eCollection 2024.

Abstract

Systemic sclerosis (SSc) is an autoimmune disease characterized by immune dysregulation, vascular damage, and fibrosis. B cells play a significant role in SSc through autoantibody production, cytokine secretion, and T cell regulation. Autoantibodies like anti-topoisomerase I and anti-RNA polymerase III are specific to SSc and linked to clinical features such as skin and lung involvement. B cell depletion therapies, particularly anti-CD20 antibodies like rituximab, have shown benefits in treating SSc, improving skin and lung disease symptoms. However, CD19, another B cell marker, is more widely expressed and has emerged as a promising target in autoimmune diseases. CD19-targeted therapies, such as CAR T cells and Uplizna (inebilizumab), have demonstrated potential in treating refractory autoimmune diseases, including SSc. Uplizna offers advantages over rituximab by targeting a broader range of B cells and showing higher efficacy in specific patient subsets. Clinical trials currently investigate Uplizna's effectiveness in SSc, particularly in severe cases. While these therapies offer hope, long-term safety and efficacy remain unknown. SSc is still a complex disease, but advancing B cell-targeted treatments could significantly improve patient outcomes and knowledge about the pathogenesis.

摘要

系统性硬化症(SSc)是一种自身免疫性疾病,其特征为免疫失调、血管损伤和纤维化。B 细胞通过产生自身抗体、分泌细胞因子和调节 T 细胞在 SSc 中发挥重要作用。抗拓扑异构酶 I 和抗 RNA 聚合酶 III 等自身抗体是 SSc 的特异性抗体,与皮肤和肺部受累等临床特征相关。B 细胞耗竭疗法,特别是抗 CD20 抗体如利妥昔单抗,已显示出在治疗 SSc 方面的益处,可改善皮肤和肺部疾病症状。然而,另一个 B 细胞标志物 CD19 表达更为广泛,已成为自身免疫性疾病的一个有前途的靶点。CD19 靶向疗法,如嵌合抗原受体 T 细胞和 Uplizna(inebilizumab),已在治疗难治性自身免疫性疾病,包括 SSc 方面显示出潜力。Uplizna 通过靶向更广泛的 B 细胞并在特定患者亚群中显示更高的疗效,优于利妥昔单抗。目前正在进行临床试验以评估 Uplizna 在 SSc 中的疗效,特别是在严重病例中。虽然这些疗法带来了希望,但长期安全性和疗效仍未知。SSc 仍然是一种复杂的疾病,但推进 B 细胞靶向治疗可能会显著改善患者的预后,并增加对发病机制的了解。

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