Amlodipine as an immunomodulator to enhance dendritic cell activation in cancer therapy with tumor-associated antigens.
This study explores the immunomodulatory effects of amlodipine, a widely used antihypertensive, on dendritic cell (DC) maturation and anti-tumor immunity.
APA
Wang Z, Huang X, et al. (2025). Amlodipine as an immunomodulator to enhance dendritic cell activation in cancer therapy with tumor-associated antigens.. Molecular therapy : the journal of the American Society of Gene Therapy, 33(10), 5162-5176. https://doi.org/10.1016/j.ymthe.2025.07.030
MLA
Wang Z, et al.. "Amlodipine as an immunomodulator to enhance dendritic cell activation in cancer therapy with tumor-associated antigens.." Molecular therapy : the journal of the American Society of Gene Therapy, vol. 33, no. 10, 2025, pp. 5162-5176.
PMID
40702728
Abstract
This study explores the immunomodulatory effects of amlodipine, a widely used antihypertensive, on dendritic cell (DC) maturation and anti-tumor immunity. Using flow cytometry, ELISA, and single-cell RNA sequencing, we found that amlodipine significantly promotes DC maturation, evidenced by increased CD80 and CD86 expression and upregulation of genes like CCL4 and Saa3 related to T cell activation. Furthermore, when amlodipine was administered in conjunction with indocyanine green or doxorubicin therapy in murine models of 4T1 breast cancer and CT26 colon cancer, we observed a notable activation of CD8 T cells. This combination therapy also resulted in elevated serum levels of cytokines such as tumor necrosis factor α, interferon-γ, and interleukin-12 and the upregulation of CD8 effector memory T cells indicative of a robust systemic immune activation, which ultimately contributed to the inhibition of tumor growth and a decrease in lung metastasis. Our research elucidates the immunomodulatory role of amlodipine in enhancing DC maturation and anti-tumor immune responses, suggesting a promising avenue for future cancer immunotherapy strategies and warranting further investigation in clinical trials.
MeSH Terms
Dendritic Cells; Animals; Amlodipine; Mice; Female; Antigens, Neoplasm; Immunologic Factors; Cell Line, Tumor; Lymphocyte Activation; CD8-Positive T-Lymphocytes; Disease Models, Animal; Humans; Cytokines; Neoplasms; Immunotherapy
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