首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Accumulation of immunoglobulin-containing cells in the gut mucosa and presence of faecal immunoglobulin in severe combined immunodeficient (scid) mice with T cell-induced inflammatory bowel disease (IBD)
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Accumulation of immunoglobulin-containing cells in the gut mucosa and presence of faecal immunoglobulin in severe combined immunodeficient (scid) mice with T cell-induced inflammatory bowel disease (IBD)

机译:在患有T细胞诱导性炎症性肠病(IBD)的严重合并免疫缺陷(Scid)小鼠中肠道粘膜中含有免疫球蛋白的细胞蓄积和粪便免疫球蛋白的存在

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摘要

Scid mice transplanted either with a gut wall graft or with low numbers of purified CD4+ T cells from immunocompetent syngeneic donor mice show clinical signs of IBD 3–4 months post-transplantation. The disease is mediated by mucosa-infiltrating CD4+ TCRαβ+ T cells. The pathology of 52 individual colon segments obtained from 20 gut wall- or CD4+ T cell-transplanted diseased scid mice was evaluated by histology and the numbers of infiltrating immunoglobulin-containing cells were determined. In particular, cells positive for IgM, IgA and non-inflammatory immunoglobulin isotypes such as IgG1 and IgG2b were found to accumulate in colon segments displaying the most severe histopathology, including inflammatory cellular infiltration, epithelial hyperplasia and ulcerative lesions. Compared with colon segments of normal C.B-17 mice, the lesional scid colon shows increased levels of cells positive for the IgG classes. Faecal extracts of the CD4+ T cell-transplanted scid mice revealed the presence of all six murine immunoglobulin isotypes. Disease progression was accompanied by an increased level of excreted IgM and IgG3 and decreased levels of IgA. It is concluded that locally secreted immunoglobulins may play an immunomodulating role in the pathological changes observed in the present model of T cell-induced inflammatory bowel disease.
机译:用消化道壁移植物或少量具有免疫功能的同系供体小鼠纯化的CD4 + T细胞移植的Scid小鼠在移植后3-4个月显示出IBD的临床体征。该疾病是由粘膜浸润的CD4 + TCRαβ + T细胞介导的。通过组织学评估了从20只肠壁或CD4 + T细胞移植的患病scid小鼠中获得的52个单个结肠节的病理学,并确定了含有免疫球蛋白的浸润细胞的数量。特别是,发现对IgM,IgA和非炎性免疫球蛋白同种型(例如IgG1和IgG2b)呈阳性的细胞积聚在结肠部分,表现出最严重的组织病理学,包括炎性细胞浸润,上皮增生和溃疡性病变。与正常C.B-17小鼠的结肠段相比,病灶性结肠显示出IgG类阳性细胞的水平升高。 CD4 + T细胞移植的scid小鼠的粪便提取物表明存在所有6种鼠免疫球蛋白同种型。疾病进展伴随着排泄的IgM和IgG3水平升高,IgA水平降低。结论是,局部分泌的免疫球蛋白可能在本T细胞诱导的炎症性肠病模型中观察到的病理变化中起免疫调节作用。

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