Department of Veterans Affairs Research Service Columbia, Missouri, 65212 ; Departments of Internal Medicine, University of Missouri School of Medicine Columbia, Missouri, 65212 ; Department of Biological Science, Arkansas State University, Arkansas Biosciences Institute Jonesboro, Arkansas, 72467.
Departments of Internal Medicine, University of Missouri School of Medicine Columbia, Missouri, 65212.
Immun Inflamm Dis. 2013 Oct;1(1):14-25. doi: 10.1002/iid3.5. Epub 2013 Oct 30.
IFN-γ-/-NOD.H-2h4 mice develop thyroid epithelial cell hyperplasia (TEC H/P) characterised by abnormal proliferation of thyrocytes and infiltration of thyroids by CD4+ and CD8+ T cells, macrophages and dendritic cells. CD8+ T cells from mice with severe TEC H/P transfer similar lesions to SCID recipients, whereas CD4+ T cells transfer mild TEC H/P. CD4- and CD8- deficient IFN-γ-/-NOD.H-2h4 mice were generated to determine if CD4+ T cells were required for initial activation of the CD8+ T cells that transfer TEC H/P. After 6-8 months on NaI water, only 2 of 60 CD8-/- mice developed severe TEC H/P, whereas 31 of 101 CD4-/- mice developed severe TEC H/P and fibrosis comparable in severity to that of IFN-γ-/- mice. However, splenocytes from CD4-/- mice with severe TEC H/P did not effectively transfer severe TEC H/P to SCID recipients. When CD4-/- donors were given agonistic anti-CD40 mAb, most developed severe TEC H/P and their cells transferred severe TEC H/P to SCID recipients. These results indicate that agonistic anti-CD40 can provide an important signal for activation of autoreactive CD8+ T cells that transfer severe TEC H/P. Therefore, targeting or blocking CD40 could provide effective therapy for diseases involving hyperplasia and fibrosis mediated by CD8+ T cells.
IFN-γ-/-NOD.H-2h4 小鼠发生甲状腺上皮细胞增生(TEC H/P),其特征为甲状腺细胞异常增生和 CD4+和 CD8+T 细胞、巨噬细胞和树突状细胞浸润甲状腺。来自严重 TEC H/P 小鼠的 CD8+T 细胞可将类似病变转移至 SCID 受体,而 CD4+T 细胞转移轻度 TEC H/P。为确定 CD4+T 细胞是否需要初始激活转移 TEC H/P 的 CD8+T 细胞,生成了 CD4-和 CD8-缺陷 IFN-γ-/-NOD.H-2h4 小鼠。在 NaI 水中 6-8 个月后,仅 60 只 CD8-/-小鼠中的 2 只发生严重 TEC H/P,而 101 只 CD4-/-小鼠中的 31 只发生严重 TEC H/P 和纤维化,其严重程度与 IFN-γ-/-小鼠相当。然而,来自严重 TEC H/P 且 CD4-/-小鼠的脾细胞未能有效将严重 TEC H/P 转移至 SCID 受体。当给予 CD4-/-供体激动性抗 CD40 mAb 时,大多数发生严重 TEC H/P,其细胞将严重 TEC H/P 转移至 SCID 受体。这些结果表明,激动性抗 CD40 可为转移严重 TEC H/P 的自身反应性 CD8+T 细胞的激活提供重要信号。因此,针对 CD40 或阻断 CD40 可能为涉及 CD8+T 细胞介导的增生和纤维化的疾病提供有效治疗。