Mechanisms of pathogenesis in scleroderma. I. Overproduction of interleukin 6 by fibroblasts cultured from affected skin sites of patients with scleroderma.

发病机制 硬皮病(真菌) 医学 放射免疫分析 白细胞介素 结缔组织病 免疫学 系统性硬皮病 刺激 全身性疾病 成纤维细胞 生产过剩 抗体 内分泌学 内科学 自身免疫性疾病 细胞因子 免疫病理学 体外 生物 疾病 生物化学 接种
作者
Carol A. Feghali,Kenneth L. Bost,Dennis W. Boulware,Larry Levy
出处
期刊:PubMed 卷期号:19 (8): 1207-11 被引量:148
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摘要

Fibroblasts were cultured from affected skin sites of patients with progressive systemic sclerosis (PSS), from unaffected skin sites of the same patients, and from a healthy donor. The concentration of interleukin 6 (IL-6) in culture medium conditioned by the growth of early passage cells was determined by radioimmunoassay and by quantitative bioassay. Results demonstrated that fibroblasts from affected PSS skin produce from 6 to 30-fold higher levels of biologically active IL-6 compared to unaffected and control cells. In contrast, serum IL-6 concentrations in 6 of 8 patients examined were not significantly different from healthy donors. Serum IL-6 levels were elevated 2 to 3-fold in 2 of 8 patients examined. Thus, the overproduction of IL-6 by affected scleroderma fibroblasts does not necessarily correlate with a systemic increase in IL-6, but may increase its concentration locally. In view of its biological activities, including stimulation of antibody production and T cell activation, the overproduction of IL-6 by PSS fibroblasts in the lesions may play a significant role in the pathogenesis of PSS and may profoundly influence the course of the disease.

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