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聚肌苷酸-聚胞苷酸及免疫细胞过继转移对Lew.1AR1-iddm大鼠及其同基因LEW.1AR1背景品系的影响。

Effects of polyinosinic-polycytidylic acid and adoptive transfer of immune cells in the Lew.1AR1-iddm rat and in its coisogenic LEW.1AR1 background strain.

作者信息

Wedekind Dirk, Weiss Heike, Jörns Anne, Lenzen Sigurd, Tiedge Markus, Hedrich Hans-Jürgen

机构信息

Institute of Laboratory Animal Science, Hannover Medical School, D-30623 Hannover, Germany.

出版信息

Autoimmunity. 2005 Jun;38(4):265-75. doi: 10.1080/08916930500114321.

Abstract

The importance of the cellular immune system for the development of T1DM in the LEW.1AR1-iddm rat was investigated by use of polyinosinic-polycytidylic acid (Poly I:C) and by adoptive transfer of concanavalin A (Con A) activated lymphocytes from diabetic LEW.1AR1-iddm rats and the coisogenic LEW.AR1 background strain. Poly I:C treatment induced diabetes, characterized morphologically by a diffuse infiltration of the pancreas, in up to 20% of the animals of the coisogenic LEW.1AR1 background strain. It did not increase the diabetes incidence of 30% of the LEW.1AR1-iddm strain. In contrast Poly I:C treatment induced diabetes in up to 80% of the animals of the Mhc congenic LEW.1WR1 strain. Adoptive transfer of lymphocytes activated by the T-cell mitogen Con A from diabetic donors doubled the incidence of diabetes, characterized morphologically by a focal insulitis, in diabetes prone LEW.1AR1-iddm recipients. In contrast, animals of the LEW.1AR1 background strain did not develop diabetes after adoptive transfer. Moreover, adoptive transfer of Con A activated lymphocytes from LEW.1AR1 rats to LEW.1AR1-iddm rats with 30 or 60% diabetes incidence, significantly decreased the incidence of diabetes in LEW.1AR1-iddm rats with 60% diabetes incidence. The results show that autoreactive lymphocytes induce beta cell destruction in the LEW.1AR1-iddm rat, while the LEW.AR1 background strain apparently contains regulatory potential, which is able to counteract the autoimmune response.

摘要

通过使用聚肌苷酸-聚胞苷酸(Poly I:C)以及从糖尿病LEW.1AR1-iddm大鼠和同基因LEW.AR1背景品系中过继转移伴刀豆球蛋白A(Con A)激活的淋巴细胞,研究了细胞免疫系统在LEW.1AR1-iddm大鼠1型糖尿病(T1DM)发病中的重要性。Poly I:C处理在高达20%的同基因LEW.1AR1背景品系动物中诱发了糖尿病,其形态学特征为胰腺弥漫性浸润。它并未增加30%的LEW.1AR1-iddm品系的糖尿病发病率。相比之下,Poly I:C处理在高达80%的Mhc同基因LEW.1WR1品系动物中诱发了糖尿病。将来自糖尿病供体经T细胞有丝分裂原Con A激活的淋巴细胞过继转移,使糖尿病易感的LEW.1AR1-iddm受体中糖尿病的发病率加倍,其形态学特征为局灶性胰岛炎。相比之下,LEW.1AR1背景品系的动物在过继转移后未发生糖尿病。此外,将来自LEW.1AR1大鼠的Con A激活淋巴细胞过继转移到糖尿病发病率为30%或60%的LEW.1AR1-iddm大鼠中,显著降低了糖尿病发病率为60%的LEW.1AR1-iddm大鼠的糖尿病发病率。结果表明,自身反应性淋巴细胞在LEW.1AR1-iddm大鼠中诱导β细胞破坏,而LEW.AR1背景品系显然具有调节潜能,能够抵消自身免疫反应。

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