CAR T-Cell Immunotherapy Treating T-ALL: Challenges and Opportunities

被引:15
作者
Ren, Anqi [1 ]
Tong, Xiqin [2 ]
Xu, Na [1 ]
Zhang, Tongcun [1 ,3 ,4 ]
Zhou, Fuling [1 ,2 ]
Zhu, Haichuan [1 ]
机构
[1] Wuhan Univ Sci & Technol, Inst Biol & Med, Coll Life & Hlth Sci, Wuhan 430081, Peoples R China
[2] Zhongnan Hosp Wuhan Univ, Dept Hematol, Wuhan 430071, Peoples R China
[3] Tianjin Univ Sci & Technol, Coll Biotechnol, Key Lab Ind Fermentat Microbiol, Minist Educ, Tianjin 300457, Peoples R China
[4] Tianjin Univ Sci & Technol, Coll Biotechnol, Tianjin Key Lab Ind Microbiol, Tianjin 300457, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
immunotherapy; T-ALL; CAR T; fratricide; T-cell aplasia; product contamination; ACUTE LYMPHOBLASTIC-LEUKEMIA; CHRONIC MYELOID-LEUKEMIA; PD-1; BLOCKADE; STEM-CELLS; I TREAT; B-CELL; RECEPTOR; ANTIGEN; EXPRESSION; THERAPY;
D O I
10.3390/vaccines11010165
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T-cell acute lymphoblastic leukemia (T-ALL), a form of T-cell malignancy, is a typically aggressive hematological malignancy with high rates of disease relapse and a poor prognosis. Current guidelines do not recommend any specific treatments for these patients, and only allogeneic stem cell transplant, which is associated with potential risks and toxicities, is a curative therapy. Recent clinical trials showed that immunotherapies, including monoclonal antibodies, checkpoint inhibitors, and CAR T therapies, are successful in treating hematologic malignancies. CAR T cells, which specifically target the B-cell surface antigen CD19, have demonstrated remarkable efficacy in the treatment of B-cell acute leukemia, and some progress has been made in the treatment of other hematologic malignancies. However, the development of CAR T-cell immunotherapy targeting T-cell malignancies appears more challenging due to the potential risks of fratricide, T-cell aplasia, immunosuppression, and product contamination. In this review, we discuss the current status of and challenges related to CAR T-cell immunotherapy for T-ALL and review potential strategies to overcome these limitations.
引用
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页数:17
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