| Literature DB >> 36173527 |
Zhu Li1, Xuemei Chen2, Luning Liu2, Meiling Zhou2, Guangqian Zhou3, Tao Liu4.
Abstract
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.Entities:
Keywords: Cancer vaccine; Cytotherapy; Induced pluripotent stem cells; T-ALL
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Year: 2022 PMID: 36173527 DOI: 10.1007/s12032-022-01809-6
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.738