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Updated: Feb 14, 2026

Assessment of the Metabolic Profile of Primary Leukemia Cells
Published on: November 21, 2018
Immunogenicity moderation effect of interleukin-24 on myelogenous leukemia cells
Xin Yu1,2, Jingcheng Miao2, Wei Xia1
1Blood Transfusion Research Institute, Wuxi Red Cross Blood Center, Wuxi.
Insights
Interleukin-24 (IL-24) enhances myelogenous leukemia cell immunogenicity, boosting their sensitivity to immune attack. This antitumor gene also inhibits tumor growth and metastasis, suggesting its potential in hematologic malignancy immunotherapy.
Area of Science:
- Oncology
- Immunology
- Gene Therapy
Background:
- Interleukin-24 (IL-24) exhibits known tumor-suppressing properties.
- The immunomodulatory effects of IL-24 on malignant cells, particularly leukemia, require further investigation.
Purpose of the Study:
- To explore the role of IL-24 in modulating the immunogenicity of myelogenous leukemia cells.
- To assess the potential of IL-24 as an immunotherapy agent for hematologic malignancies.
Main Methods:
- Investigated IL-24's effect on leukemia cell immunogenicity markers.
- Assessed IL-24's impact on cytokine production and sensitivity to immune effector cells.
- Evaluated IL-24's in vivo anti-tumor activity and effects on angiogenesis and metastasis factors.
Main Results:
- IL-24 treatment enhanced leukemia cell immunogenicity and cytokine production.
- IL-24 increased sensitivity of leukemia cells to immune effector cells.
- In vivo, IL-24 expression suppressed transplanted leukemia tumor growth and downregulated angiogenesis and metastasis-related proteins.
Conclusions:
- IL-24 significantly enhances leukemia cell immunogenicity and anti-tumor immune responses.
- IL-24 demonstrates potential as a therapeutic agent for hematologic malignancy immunotherapy.
- Further clinical trials of IL-24 for hematologic malignancies are warranted.
Abstract:
Previous studies have shown that interleukin-24 (IL-24) has tumor-suppressing activity by multiple pathways. However, the immunogenicity moderation effect of IL-24 on malignant cells has not been explored extensively. In this study, we investigated the role of IL-24 in immunogenicity modulation of the myelogenous leukemia cells. Data show that myelogenous leukemia cells express low levels of immunogenicity molecules. Treatment with IL-24 could enhance leukemia cell immunogenicity, predominantly regulate leukemia cells to produce immune-associated cytokines, and improve the cytotoxic sensitivity of these cells to immune effector cells. IL-24 expression could retard transplanted leukemia cell tumor growth in vivo in athymic nude mice. Moreover, IL-24 had marked effects on downregulating the expression of angiogenesis-related proteins vascular endothelial growth factor, cluster of differentiation (CD) 31, CD34, collagen IV and metastasis-related factors CD147, membrane type-1 matrix metalloproteinase (MMP), and MMP-2 and MMP-9 in transplanted tumors. These findings indicated novel functions of this antitumor gene and characterized IL-24 as a promising agent for further clinical trial for hematologic malignancy immunotherapy.
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