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Interleukin 15 activity in the rectal mucosa of inflammatory bowel disease
Authors:Tetsu Sakai  Kazuo Kusugami  Hitoshi Nishimura  Takafumi Ando  Takeo Yamaguchi  Masahiro Ohsuga  Kenji Ina  Atsushi Enomoto  Yuki Kimura  Yasunobu Yoshikai
Affiliation:*First Department of Internal Medicine;Laboratory of Host Defense and Germfree Life, Research Institute for Disease Mechanism and Control, Nagoya University School of Medicine, Nagoya, Japan
Abstract:Background & Aims: Interleukin (IL)-15 has been found to share many immunoregulatory activities in lymphocytes with IL-2. The aim of this study was to investigate IL-15 activity in organ cultures, localization of IL-15 messenger RNA (mRNA), and proliferation of lamina propria mononuclear cells (LPMCs) in response to recombinant IL-15 using the mucosal tissues obtained from patients with inflammatory bowel disease (IBD). Methods: The contents of IL-15, tumor necrosis factor α, and IL-2 in the culture supernatant of the rectal mucosal tissues were determined by an enzyme-linked immunosorbent assay. Expression of IL-15 mRNA was analyzed by in situ hybridization, and proliferative response of LPMCs to recombinant IL-15 was determined by [3H]thymidine incorporation into DNA. Results: Significantly greater IL-15 activity was detected in active IBD, and this elevation was also observed in inactive ulcerative colitis. In contrast, greater tumor necrosis factor α activity was observed only in active IBD, and IL-2 was not detected in organ cultures. In situ hybridization showed IL-15 mRNA in macrophages and epithelial cells in active IBD specimens, and recombinant IL-15 induced a dose-dependent proliferative response in LPMCs. Conclusions: Mucosal IL-15 may be involved in the pathogenesis of IBD as one of the important mediators in activation of mucosal immune cells.GASTROENTEROLOGY 1998;114:1237-1243
Keywords:Abbreviations: ELISA, enzyme-linked immunosorbent assay   IC, inflammatory control   IL, interleukin   IL-2R, interleukin 2 receptor   LPMC, lamina propria mononuclear cell   r, recombinant   TNF-α, tumor necrosis factor α
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