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通过白细胞介素-2受体表达来衡量的乳糜泻中淋巴细胞对麸质组分111的激活。

Lymphocyte activation as measured by interleukin-2 receptor expression to gluten fraction 111 in coeliac disease.

作者信息

Penttila I A, Gibson C E, Forrest B D, Cummins A G, LaBrooy J T

机构信息

Department of Medicine, Royal Adelaide Hospital, Australia.

出版信息

Immunol Cell Biol. 1990 Jun;68 ( Pt 3):155-60. doi: 10.1038/icb.1990.22.

Abstract

Lymphocyte activation was examined by interleukin-2 (IL-2) receptor expression on peripheral blood mononuclear cells from coeliac and control subjects. Purified T cells were incubated with gluten fraction 111 (a known toxic peptide for coeliac subjects), soyabean hydrolysate (an unrelated hydrolysed food antigen), and Concanavalin-A (Con-A, a non-specific mitogen). After 1-5 days incubation, expression of IL-2 receptors was assessed using a cellular enzyme-linked immunosorbent assay (ELISA). Gluten fraction 111 induced expression of IL-2 receptors on T lymphocytes from coeliac but not from normal subjects (P = 0.0005), whereas soyabean hydrolysate did not induce IL-2 receptor expression. Lymphocytes from both coeliac and normal subjects had similar increased IL-2 receptor expression after incubation with Con-A. Flow cytometry was also used to confirm specific expression of IL-2 receptor expression of lymphocytes from coeliac subjects. Interleukin-2 receptor expression increased from 0 to 5.4% of cultured mononuclear cells after 7 days incubation with gluten fraction III. These cells were CD3-positive and CD4-positive. We conclude that peripheral blood lymphocytes from coeliac subjects are sensitized specifically to gluten fraction III.

摘要

通过检测腹腔疾病患者和对照受试者外周血单个核细胞上白细胞介素-2(IL-2)受体的表达来研究淋巴细胞活化情况。将纯化的T细胞与麸质组分III(腹腔疾病患者已知的毒性肽)、大豆水解物(一种无关的水解食物抗原)和刀豆球蛋白A(Con-A,一种非特异性有丝分裂原)一起孵育。孵育1-5天后,使用细胞酶联免疫吸附测定(ELISA)评估IL-2受体的表达。麸质组分III诱导腹腔疾病患者而非正常受试者的T淋巴细胞上IL-2受体的表达(P = 0.0005),而大豆水解物未诱导IL-2受体表达。与Con-A孵育后,腹腔疾病患者和正常受试者的淋巴细胞IL-2受体表达均有类似增加。流式细胞术也用于确认腹腔疾病患者淋巴细胞IL-2受体表达的特异性。与麸质组分III孵育7天后,培养的单个核细胞中IL-2受体表达从0增加到5.4%。这些细胞CD3阳性且CD4阳性。我们得出结论,腹腔疾病患者的外周血淋巴细胞对麸质组分III具有特异性致敏作用。

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