Application of chimeric antigen receptor modified mesenchymal stem cells in preparation of drugs for treating systemic lupus erythematosus

By expressing the chimeric antigen receptor CAR1 targeting B cells on mesenchymal stem cells and activating the JAK-STAT1 pathway, the individual response variability of MSCs therapy in SLE treatment and the risks of CAR-T therapy were addressed, achieving stable immunosuppressive effects, expanding the scope of application and improving safety.

CN122399015APending Publication Date: 2026-07-17INSTITUTE OF BASIC MEDICAL SCIENCES CHINESE ACADEMY OF MEDICAL SCIENCES
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
INSTITUTE OF BASIC MEDICAL SCIENCES CHINESE ACADEMY OF MEDICAL SCIENCES
Filing Date
2025-01-16
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing MSCs therapies for the treatment of systemic lupus erythematosus (SLE) exhibit significant individual variability and are greatly influenced by the inflammatory environment. CAR-T therapy carries clinical risks and side effects, and the applicability of existing gene-modified MSCs therapies is limited.

Method used

By using chimeric antigen receptor-modified mesenchymal stem cells (CAR1-MSCs), the CD19 antigen targeting B cells is expressed on the surface of MSCs through genetic engineering and the JAK-STAT1 pathway is activated to achieve stable immunosuppressive function.

Benefits of technology

CAR1-MSCs exhibit stable B-cell-specific immunosuppressive capacity in vitro, reducing the impact of T-cell activation, expanding the applicability of MSCs therapy, and improving the efficacy and safety of SLE treatment.

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Abstract

本发明属于生物医药技术领域,具体涉及嵌合抗原受体修饰的间充质干细胞在制备治疗系统性红斑狼疮药物中的应用,所述嵌合抗原受体由胞外段和胞内段组成;所述胞外段为靶向B细胞表面CD19抗原单链抗体;所述胞内段为可激活JAK‑STAT1通路的IFNγ受体的胞内部分,本发明具有以下优点:嵌合抗原受体修饰的间充质干细胞结合了CAR‑T疗法和间充质干细胞疗法的双重优势,既能稳定地表现出免疫抑制功能,又能避免对B细胞的长期剧烈的杀伤作用,提升了细胞疗法的稳定性、安全性和普适性,有望成为SLE治疗的更优选择。
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