LILRB4 as a novel immunotherapeutic target for multiple diseases

被引:0
|
作者
Wang, Xu [1 ,2 ,3 ]
Li, Lanying [1 ,2 ,3 ]
Liu, Dan [1 ,2 ,3 ]
Jin, Yuhang [1 ,2 ,3 ]
Zhao, Xuan [1 ,2 ,3 ]
Li, Sijin [1 ,2 ,3 ]
Hou, Rui [4 ]
Guan, Zhangchun [1 ,2 ,3 ]
Ma, Wen [1 ,2 ,3 ]
Zheng, Junnian [1 ,2 ,3 ]
Lv, Ming [1 ,5 ]
Shi, Ming [1 ,2 ,3 ]
机构
[1] Xuzhou Med Univ, Canc Inst, 209 Tongshan Rd, Xuzhou 221004, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Affiliated Hosp, Ctr Clin Oncol, 99 Huaihai Rd, Xuzhou 221002, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Jiangsu Ctr Collaborat & Innovat Canc Biotherapy, 209 Tongshan Rd, Xuzhou 221004, Jiangsu, Peoples R China
[4] Xuzhou Med Univ, Coll Pharm, Xuzhou, Jiangsu, Peoples R China
[5] Hangzhou Sumgen Biotech Co Ltd, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Emerging Immune checkpoints; LILRB4; Multiple diseases; Immunotherapy; Adoptive therapy; INHIBITORY RECEPTOR ILT3; T-CELL THERAPY; IMMUNOGLOBULIN-LIKE RECEPTORS; ACUTE MYELOID-LEUKEMIA; VERSUS-HOST-DISEASE; DENDRITIC CELLS; IMMUNE-CHECKPOINT; TRANSCRIPT; EXPRESSION; ACTIVATION;
D O I
10.1016/j.bcp.2025.116762
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Immune checkpoints are critical for maintaining autoimmune homeostasis and are implicated in various auto- immune diseases, with their significance increasingly recognized. Investigating the functions and mechanisms of these checkpoints is essential for the development of more effective treatments. Leukocyte immunoglobulin-like receptor subfamily B member 4 (LILRB4) stands out as a unique immune checkpoint, with limited expression in most normal tissues but prominent presence in various hematological and solid tumors. It is also expressed on numerous immune and stromal cells, functioning as both a "Tumor Immune Checkpoint" and a "Tumor Stromal Immune Checkpoint." Due to its distinct expression profile, LILRB4 plays a pivotal role in tumors, autoimmune diseases, allergic reactions, and the maintenance of immune homeostasis during transplantation and pregnancy. A thorough understanding of its ligands, functions, mechanisms, and ongoing therapeutic strategies targeting LILRB4 will be crucial for the development of advanced therapeutic options. This review examines LILRB4 expression and function across multiple diseases and discusses therapeutic approaches targeting LILRB4 in various contexts. Additionally, the potential of combining current drugs with LILRB4-targeted therapies is explored. Challenges in developing LILRB4-targeting drugs are also addressed, offering valuable insights for future research.
引用
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页数:13
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