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共济失调毛细血管扩张症中干扰素-γ产生缺陷。

Defective interferon-gamma production in ataxia-telangiectasia.

作者信息

Paganelli R, Capobianchi M R, Matricardi P M, Cioè L, Seminara R, Dianzani F, Aiuti F

出版信息

Clin Immunol Immunopathol. 1984 Sep;32(3):387-91. doi: 10.1016/0090-1229(84)90282-4.

Abstract

The in vitro production of interferon-alpha and -gamma (IFN) by peripheral blood mononuclear cells from four patients with ataxia-telangiectasia was compared to that of healthy controls. Normal values of IFN-alpha were obtained in all cases. However, patients with ataxia-telangiectasia showed a great reduction or absence of IFN-gamma production after induction with either staphylococcal enterotoxin B or galactose oxidase. This defect was accompanied by the absence of secretion of another lymphokine, namely, interleukin 2 (IL-2), in one case. Lymphoproliferative response to phytohemagglutinin (PHA) was severely depressed in all patients. Near normal values of T lymphocytes were found, but the ratio of OKT4+/OKT8+ subsets was reduced in most patients, due to a decrease of OKT4+ lymphocytes. Deficiency of IFN-gamma may contribute to the abnormalities of immune functions and immunoregulation observed in ataxia-telangiectasia, and it may represent an additional cause of the high incidence of viral infections and neoplasia in this disease.

摘要

将四名共济失调毛细血管扩张症患者外周血单个核细胞产生干扰素α和γ(IFN)的体外情况与健康对照者进行了比较。所有病例中均获得了正常的干扰素α值。然而,在用葡萄球菌肠毒素B或半乳糖氧化酶诱导后,共济失调毛细血管扩张症患者的干扰素γ产生大幅减少或缺失。在一个病例中,这种缺陷伴随着另一种淋巴因子即白细胞介素2(IL-2)分泌的缺失。所有患者对植物血凝素(PHA)的淋巴细胞增殖反应均严重受抑。发现T淋巴细胞值接近正常,但大多数患者OKT4+/OKT8+亚群的比例降低,原因是OKT4+淋巴细胞减少。干扰素γ缺乏可能导致共济失调毛细血管扩张症中观察到的免疫功能和免疫调节异常,并且它可能是该疾病中病毒感染和肿瘤高发病率的另一个原因。

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