Abstract
Low doses of the alkylating agent cyclophosphamide (CTX) mediate antiangiogenic and immunostimulatory effects, leading to potent tumoricidal activity in association with various immunotherapeutic strategies. Here, we show in rodents and cancer patients that CTX markedly promotes the differentiation of CD4(+) T helper 17 (Th17) cells that can be recovered in both blood and tumor beds. However, CTX does not convert regulatory T cells into Th17 cells. Because Th17 are potent inducers of tissue inflammation and autoimmunity, these results suggest impact on the clinical management of various types of malignancies treated with alkylating agents and a potential need to optimize CTX-based immunotherapy in patients.
Publication types
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Clinical Trial, Phase I
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Animals
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Antineoplastic Agents, Alkylating / administration & dosage
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Antineoplastic Agents, Alkylating / pharmacology*
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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Benzamides
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Cell Differentiation / drug effects*
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Cell Differentiation / immunology
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Cyclophosphamide / administration & dosage
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Cyclophosphamide / pharmacology*
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Female
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Humans
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Imatinib Mesylate
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Interleukin-2 / administration & dosage
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Lymphocyte Subsets / drug effects
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Lymphocyte Subsets / immunology
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Male
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Melanoma, Experimental / drug therapy
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Melanoma, Experimental / immunology
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Mice
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Mice, Inbred C57BL
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Middle Aged
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Neoplasms / drug therapy*
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Neoplasms / immunology*
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Piperazines / administration & dosage
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Pyrimidines / administration & dosage
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T-Lymphocytes, Regulatory / drug effects
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T-Lymphocytes, Regulatory / immunology
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Th17 Cells / drug effects*
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Th17 Cells / pathology
Substances
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Antineoplastic Agents, Alkylating
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Benzamides
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Interleukin-2
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Piperazines
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Pyrimidines
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Imatinib Mesylate
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Cyclophosphamide