Yoon Ji-Won, Jun Hee-Sook
Rosalind Franklin Comprehensive Diabetes Center, Chicago Medical School, North Chicago, IL 60064, USA.
Ann N Y Acad Sci. 2006 Oct;1079:138-46. doi: 10.1196/annals.1375.021.
More than 10 viruses have been reported to be associated with the development of type 1 diabetes-like symptoms in animals, with the best evidence coming from studies on the D variant of encephalomyocarditis (EMC-D) virus in mice and Kilham rat virus (KRV) in rats. A high titer of EMC-D viral infection results in the development of diabetes within 3 days, primarily due to the rapid destruction of beta cells by viral replication within the cells. A low titer of EMC-D viral infection results in the recruitment of macrophages to the islets. Soluble mediators produced by activated macrophages play a critical role in the destruction of residual beta cells. A single amino acid at position 776 of the EMC viral genome controls the diabetogenicity of the virus. In contrast, KRV causes autoimmune type 1 diabetes in diabetes-resistant BioBreeding (DR-BB) rats without direct infection of beta cells. Macrophages play an important role in the development of diabetes in KRV-infected DR-BB rats. As well, KRV infection preferentially activates effector T cells, such as Th1-like CD45RC(+)CD4(+) T cells and CD8(+) T cells, and downregulates regulatory T cells, such as Th2-like CD45RC(-)CD4(+) T cells. This results in the breakdown of the immune balance, contributing to the development of diabetes in KRV-infected DR-BB rats.
据报道,超过10种病毒与动物1型糖尿病样症状的发展有关,其中最有力的证据来自对小鼠脑心肌炎病毒D变体(EMC-D)和大鼠基尔汉姆大鼠病毒(KRV)的研究。高滴度的EMC-D病毒感染会在3天内导致糖尿病的发生,主要是由于病毒在细胞内复制导致β细胞迅速被破坏。低滴度的EMC-D病毒感染会导致巨噬细胞募集到胰岛。活化的巨噬细胞产生的可溶性介质在残余β细胞的破坏中起关键作用。EMC病毒基因组第776位的单个氨基酸控制着病毒的致糖尿病性。相比之下,KRV在抗糖尿病的BioBreeding(DR-BB)大鼠中引发自身免疫性1型糖尿病,而不会直接感染β细胞。巨噬细胞在KRV感染的DR-BB大鼠糖尿病的发展中起重要作用。此外,KRV感染优先激活效应T细胞,如Th1样CD45RC(+)CD4(+) T细胞和CD8(+) T细胞,并下调调节性T细胞,如Th2样CD45RC(-)CD4(+) T细胞。这导致免疫平衡的破坏,促成KRV感染的DR-BB大鼠糖尿病的发展。