Small-Molecule Compounds Boost CAR-T Cell Therapy in Hematological Malignancies

被引:13
|
作者
Cao, Xinping [1 ]
Jin, Xin [2 ]
Zhang, Xiaomei [3 ]
Utsav, Paudel [1 ]
Zhang, Yi [1 ]
Guo, Ruiting [1 ]
Lu, Wenyi [2 ]
Zhao, Mingfeng [2 ]
机构
[1] Tianjin Med Univ, Ctr Clin Coll 1, Tianjin 300192, Peoples R China
[2] Tianjin First Cent Hosp, Dept Hematol, Tianjin 300192, Peoples R China
[3] Nankai Univ, Sch Med, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Chimeric antigen receptor T cells; Hematological malignancies; Small-molecule compounds; CHIMERIC ANTIGEN RECEPTOR; BRUTONS TYROSINE KINASE; INHIBITOR IBRUTINIB; MTOR INHIBITORS; HDAC INHIBITORS; CANCER; EXPRESSION; LYMPHOMA; RESISTANT; PROTEIN;
D O I
10.1007/s11864-023-01049-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Opinion statementAlthough chimeric antigen receptor T cell immunotherapy has been successfully applied in patients with hematological malignancies, several obstacles still need to be overcome, such as high relapse rates and side effects. Overcoming the limitations of CAR-T cell therapy and boosting the efficacy of CAR-T cell therapy are urgent issues that must be addressed. The exploration of small-molecule compounds in combination with CAR-T cell therapies has achieved promising success in pre-clinical and clinical studies in recent years. Protein kinase inhibitors, demethylating drugs, HDAC inhibitors, PI3K inhibitors, immunomodulatory drugs, Akt inhibitors, mTOR inhibitors, and Bcl-2 inhibitors exhibited potential synergy in combination with CAR-T cell therapy. In this review, we will discuss the recent application of these combination therapies for improved outcomes of CAR-T cell therapy.
引用
收藏
页码:184 / 211
页数:28
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