Suppr超能文献

免疫调节治疗对MRL/Mp-lpr/lpr小鼠自身免疫性涎腺炎的影响。

Effects of immunomodulating treatment on autoimmune sialadenitis in MRL/Mp-lpr/lpr mice.

作者信息

Jonsson R, Tarkowski A, Bäckman K

机构信息

Department of Oral Pathology, Faculty of Odontology, University of Göteborg, Sweden.

出版信息

Agents Actions. 1988 Dec;25(3-4):368-74. doi: 10.1007/BF01965044.

Abstract

The autoimmune MRL/Mp-lpr/lpr (MRL/l) mouse spontaneously develops sialadenitis with a morphological and phenotypical pattern similar to that seen in human Sjögren's syndrome (SS). This makes the MRL/l mouse a suitable model for therapeutical studies of autoimmune sialadenitis. We have, by histological and immunohistochemical techniques, analyzed the therapeutical effect of treatment with LS2616, a recently synthesized oxokinolinamide derivative, on sialadenitis in submandibular glands of MRL/l mice. The results were compared with effects obtained after treatment with cyclophosphamide (CY) and physiologic saline. Administration of both LS2616 and CY to MRL/l mice has previously been found to result in prolongation of survival and amelioration of organ pathology. However, only CY treatment reduced sialadenitis, while LS2616 increased the semiquantitatively assessed focal inflammation of salivary glands in 6 months old mice. No differences in T-cell phenotypes of infiltrating lymphoid cells in salivary glands between different treatment regims could be noted. However, the frequency of B-cells in the sialadenitis was decreased in the CY treated group. In contrast, CY but not LS2616 treatment normalized expression of T-helper and cytotoxic T-cell phenotypes as well as reduced the B-cell portion in lymph nodes. It is concluded that CY treatment can suppress sialadenitis although both LS2616 and CY are effective in prolongation lifespan of MRL/l mice. This may implicate different immunopathogenic mechanisms for development of sialadenitis versus other organ lesions in the autoimmune disease of MRL/l mice.

摘要

自身免疫性MRL/Mp-lpr/lpr(MRL/l)小鼠会自发发生涎腺炎,其形态和表型模式与人类干燥综合征(SS)相似。这使得MRL/l小鼠成为自身免疫性涎腺炎治疗研究的合适模型。我们通过组织学和免疫组化技术,分析了最近合成的氧代喹啉酰胺衍生物LS2616对MRL/l小鼠下颌下腺涎腺炎的治疗效果。将结果与环磷酰胺(CY)和生理盐水治疗后的效果进行了比较。先前发现给MRL/l小鼠施用LS2616和CY均能延长生存期并改善器官病理状况。然而,只有CY治疗能减轻涎腺炎,而LS2616却增加了6月龄小鼠唾液腺半定量评估的局灶性炎症。不同治疗方案之间,唾液腺中浸润淋巴细胞的T细胞表型没有差异。然而,CY治疗组涎腺炎中B细胞的频率降低。相反,CY治疗而非LS2616治疗使辅助性T细胞和细胞毒性T细胞表型的表达正常化,并减少了淋巴结中的B细胞比例。结论是,尽管LS2616和CY都能有效延长MRL/l小鼠的寿命,但CY治疗能抑制涎腺炎。这可能意味着在MRL/l小鼠自身免疫性疾病中,涎腺炎与其他器官病变的发生存在不同的免疫致病机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验