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肾脏病与透析肾移植杂志 ›› 2026, Vol. 35 ›› Issue (3): 276-281.DOI: 10.3969/j.issn.1006-298X.2026.03.015

• 肾脏病临床 • 上一篇    下一篇

CD38 与系统性红斑狼疮的研究进展

  

  • 出版日期:2026-06-29 发布日期:2026-07-02

Research progress of CD38 in systemic lupus erythematosus

  • Online:2026-06-29 Published:2026-07-02

摘要: 系统性红斑狼疮 (SLE) 是一种高度异质性、累及多系统的自身免疫性疾病。尽管传统免疫抑制治疗取得一定进展,但复发率高和完全缓解率低仍是临床挑战。CD38 作为一种兼具酶学活性、受体功能和黏附分子特性的跨膜糖蛋白,在 SLE 的免疫病理机制中扮演着关键角色。本综述系统阐述了 CD38 的分子生物学特征及其在 SLE 免疫细胞的异常表达,重点关注近年来靶向 CD38 单克隆抗体 (如达雷妥尤单抗、美扎吉单抗、CM313 等) 在 SLE 及其相关肾脏疾病治疗中的研究进展,探讨了其疗效、安全性及存在的主要挑战。CD38 靶向治疗有望打破传统疗法的局限,为难治性 SLE 提供新的治疗方案。

关键词: 系统性红斑狼疮, CD38, 靶向治疗, 单克隆抗体, 狼疮肾炎

Abstract: Systemic lupus erythematosus (SLE) is a heterogeneous autoimmune disease characterized by multisystem involvement. Despite advances in conventional immunosuppressive therapies, achieving sustained remission remains challenging because of high relapse rates and suboptimal complete remission rates. CD38, a transmembrane glycoprotein with enzymatic, receptor, and adhesion functions, plays an important role in the immunopathogenesis of SLE. This review summarizes the molecular characteristics of CD38 and its aberrant expression in immune cell subsets of patients with SLE. Particular emphasis is placed on recent advances in anti-CD38 monoclonal antibody therapies, including daratumumab, mezagitamab, and CM313, for the treatment of SLE and lupus nephritis. The efficacy, safety, and current limitations of these therapeutic strategies are also discussed. Emerging evidence suggests that CD38-targeted therapies may provide a promising treatment option for refractory SLE and contribute to the development of more precise immunotherapeutic approaches.

Key words: systemic lupus erythematosus, CD38, targeted therapy, monoclonal antibody, lupus nephritis

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