Development of the T-ALLiPSC-based therapeutic cancer vaccines for T-cell acute lymphoblastic leukemia

被引:2
|
作者
Li, Zhu [1 ,2 ]
Chen, Xuemei [3 ]
Liu, Luning [3 ]
Zhou, Meiling [3 ]
Zhou, Guangqian [1 ,2 ]
Liu, Tao [1 ,2 ]
机构
[1] Shenzhen Univ, Hlth Sci Ctr, Dept Med Cell Biol & Genet, Guangdong Key Lab Genom Stabil & Dis Prevent,Shen, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Shenzhen Engn Lab Regenerat Technol Orthopaed Dis, Hlth Sci Ctr, Shenzhen 518060, Peoples R China
[3] Shenzhen Univ, Shenzhen Luohu Peoples Hosp, Dept Tumor Immunotherapy, Affiliated Hosp 3, Shenzhen 518001, Guangdong, Peoples R China
关键词
Induced pluripotent stem cells; Cancer vaccine; T-ALL; Cytotherapy; PLURIPOTENT STEM-CELLS; BIOLOGY;
D O I
10.1007/s12032-022-01809-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The T-cell acute lymphoblastic leukemia (T-ALL) is a kind of hematological malignancy in children. Despite the significant improvement in the cure rate of T-ALL upon treatment with chemotherapy regimens, steroids, and allotransplantation there are relapses. This study focuses on the tumor-specific therapeutic vaccines derived from the induced pluripotent stem cells (iPSC) to address the issue of T-ALL recurrence. Patient-derived tumor cells and healthy donor cells were reprogrammed into the iPSCs and the RNA-seq data of the T-ALL-iPSCs and H-iPSCs were analyzed. In vitro, the whole-cell lysate antigens of iPSCs were prepared to induce the dendritic cells (DC) maturation, which in turn stimulated the tumor-specific T cells to kill the T-ALL tumor cells (Jurkat, CCRF-CEM, MOLT-4). The cytotoxic T lymphocyte stimulated by the DC-loaded T-ALL-iPSC-derived antigens showed specific cytotoxicity against the T-ALL cells in vitro. In conclusion, the T-ALL-iPSC-based therapeutic cancer vaccine can elicit a specific anti-tumor effect on T-ALL.
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页数:11
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