4.4 Article

Therapeutic effects of vitamin D and IL-22 on methotrexate-induced mucositis in mice

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ANTI-CANCER DRUGS
卷 33, 期 1, 页码 11-18

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CAD.0000000000001128

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innate lymphoid cell; IL-22; methotrexate; mucositis; vitamin D

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Mucositis is a common side effect of cancer therapies and transplant conditioning regimens. This study investigated the therapeutic potential of vitamin D and IL-22 in a murine model of chemotherapy-induced mucositis. The results showed that daily vitamin D injections improved intestinal inflammation, while temporal overexpression of IL-22 did not provide significant protection from mucositis.
Mucositis is a common side effect of cancer therapies and transplant conditioning regimens. Management of mucositis involves multiple approaches from oral hygiene, anti-inflammatory, anti-apoptotic, cytoprotective, and antioxidant agents, to cryo-therapy, physical therapy, and growth factors. There is room for novel, affordable treatment options, or improvement of currently available therapies. Vitamin D has been shown to regulate mucosa-resident cell populations such as Th17 or innate lymphoid cells and critical mucosal cytokine IL-22; however, their therapeutic potential has not been put to test in preclinical mouse models. In this study, we aimed to test the therapeutic potential of vitamin D injections and IL-22 overexpression in a murine model of chemotherapy-induced mucositis. Balb/c mice were given daily intraperitoneal injections of vitamin D. Mucositis was induced by methotrexate. Another group received IL-22 plasmid via hydrodynamic gene delivery. Weight loss and intestinal histopathology, intestinal levels of cytokines IL-22, IL-17A, GM-CSF, IL-23, IFN-gamma, TNF-alpha, and IL-10, and number of intestinal lamina propria B cell, neutrophil, and total innate lymphoid cells were quantified. Daily vitamin D injections ameliorated intestinal inflammation and elevated intestinal IL-22 levels compared with control groups. Temporal overexpression of IL-22 by hydrodynamic gene delivery slightly increased intestinal IL-22 but failed to confer significant protection from mucositis. To our knowledge, this is the first experimental demonstration in an animal model of mucositis of therapeutic use of vitamin D and IL-22 supplementation and our results with vitamin D suggest it may have merit in further trials in human mucositis patients.

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