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人肠道黏膜单核细胞产生的干扰素γ。炎症性肠病中水平降低。

Interferon gamma production by human intestinal mucosal mononuclear cells. Decreased levels in inflammatory bowel disease.

作者信息

Lieberman B Y, Fiocchi C, Youngman K R, Sapatnekar W K, Proffitt M R

机构信息

Department of Immunology and Cancer, Cleveland Clinic Foundation, Ohio 44106.

出版信息

Dig Dis Sci. 1988 Oct;33(10):1297-304. doi: 10.1007/BF01536683.

Abstract

Immune (gamma) interferon is a substance produced by immunologically activated mononuclear cells. Besides its antiviral activity, interferon gamma has a crucial role in immunoregulation, by acting directly upon lymphocytes and monocytes, and interacting with other soluble mediators of the immune response. Studies of the interferons system in inflammatory bowel disease have been limited, and little information is available on the generation of interferon during immunological events occurring in the human gut. To investigate the capacity of intestinal mucosal mononuclear cells to produce interferon gamma, lamina proprial mononuclear cells, isolated from Crohn's disease, ulcerative colitis, and control patients, were incubated with interleukin 2 or phytohemagglutinin, and the amounts of interferon gamma present in the culture supernatants were measured by a virus cytopathic effect inhibition assay. Under identical stimulatory conditions, culture supernatants of cells derived from actively involved mucosa of inflammatory bowel disease specimens contained two- to fivefold less interferon gamma than those of cells from control tissue. However, the amount of interferon gamma present in supernatants of cells from uninvolved inflammatory bowel disease mucosa was similar to that found in control supernatants. These results indicate that, in patients with active Crohn's disease and ulcerative colitis, mononuclear cells produce decreased amounts of interferon gamma in the intestinal mucosa. The exact significance of these findings is unclear, but because of the importance of interferon gamma in a variety of cell-mediated immune phenomena, its impaired availability might be relevant to the pathogenesis of inflammatory bowel disease.

摘要

免疫(γ)干扰素是免疫激活的单核细胞产生的一种物质。除了具有抗病毒活性外,干扰素γ在免疫调节中也起着关键作用,它直接作用于淋巴细胞和单核细胞,并与免疫反应的其他可溶性介质相互作用。对炎症性肠病中干扰素系统的研究有限,关于人类肠道免疫事件期间干扰素生成的信息也很少。为了研究肠道黏膜单核细胞产生干扰素γ的能力,将从克罗恩病、溃疡性结肠炎患者及对照患者分离出的固有层单核细胞与白细胞介素2或植物血凝素一起孵育,并用病毒细胞病变效应抑制试验测定培养上清液中干扰素γ的含量。在相同的刺激条件下,炎症性肠病标本中病变活跃黏膜来源的细胞培养上清液中所含的干扰素γ比对照组织来源的细胞少两到五倍。然而,炎症性肠病未受累黏膜来源的细胞上清液中干扰素γ的含量与对照上清液中的相似。这些结果表明,在活动性克罗恩病和溃疡性结肠炎患者中,单核细胞在肠道黏膜中产生的干扰素γ量减少。这些发现的确切意义尚不清楚,但由于干扰素γ在多种细胞介导的免疫现象中具有重要作用,其可用性受损可能与炎症性肠病的发病机制有关。

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