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Updated: Jun 19, 2026

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Manufacturing Chimeric Antigen Receptor (CAR) T Cells for Adoptive Immunotherapy
Published on: December 17, 2019
[Immunotherapy and cell therapy for myeloid leukemia].
1Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine.
Nihon Rinsho. Japanese Journal of Clinical Medicine
|October 29, 2009
Summary
Identifying leukemia-associated antigens recognized by cytotoxic T lymphocytes (CTL) is crucial for effective cellular immunotherapy. Ongoing clinical trials explore various immunotherapy strategies for hematological malignancies.
Area of Science:
- Immunology
- Oncology
- Genetics
Context:
- Effective cellular immunotherapy for hematopoietic malignancies requires identification of tumor-associated antigens.
- Cytotoxic T lymphocytes (CTL) recognize specific antigens in the context of HLA class I molecules.
Purpose:
- To review the current status and future potential of cellular immunotherapy for leukemia.
- To highlight identified leukemia-associated antigens and ongoing clinical trials.
Summary:
- Various leukemia-associated antigens, including fusion gene products (e.g., BCR-ABL, ETV6-AML1), proteinase 3, WT1, human telomerase reverse transcriptase, cyclophilin B, and PRAME, have been identified.
- Clinical trials are investigating peptide vaccination, dendritic cell therapy, adoptive CTL transfer, and T-cell receptor gene therapy for hematological malignancies.
Impact:
- Advances in identifying tumor antigens are paving the way for novel cellular immunotherapies.
- This research supports the development of targeted treatments for leukemia and other blood cancers.
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