Tada Yoshifumi, Koarada Syuichi, Tomiyoshi Yoshiyuki, Morito Fumitaka, Mitamura Mio, Haruta Yoshio, Ohta Akihide, Nagasawa Kohei
Department of Internal Medicine, Saga Medical School, 5-1-1 Nabeshima, Saga 849-8501, Japan.
Clin Immunol. 2006 Aug;120(2):179-88. doi: 10.1016/j.clim.2006.02.009. Epub 2006 Apr 17.
Inducible costimulator (ICOS) is a costimulatory molecule expressed in activated T cells and plays an important role in T-cell-dependent immune responses. We investigated the role of ICOS in the development of autoimmune diseases in MRL/Mpj-lpr/lpr (MRL/lpr) mice. ICOS was expressed on CD4(+) T cells from adult MRL/lpr mice. ICOS-deficient MRL/lpr mice showed mild lymphoadenopathy and a decreased memory type CD4(+) T cells in the spleen. The anti-dsDNA antibody levels were decreased. CD4(+) T cells from ICOS-deficient MRL/lpr mice showed less of a bias to Th1 and an enhanced production of IL-4 in response to anti-CD3 antibody in comparison to those from wild-type MRL/lpr mice. Although ICOS-deficiency abrogated renal vasculitis completely, the severity of glomerulonephritis was not altered. ICOS is considered to play a role in CD4(+) T cell activation, autoantibody production, and renal vasculitis. However, it is not essentially required in the development of glomerulonephritis.
诱导性共刺激分子(ICOS)是一种在活化T细胞中表达的共刺激分子,在T细胞依赖性免疫反应中起重要作用。我们研究了ICOS在MRL/Mpj-lpr/lpr(MRL/lpr)小鼠自身免疫性疾病发展中的作用。ICOS在成年MRL/lpr小鼠的CD4(+) T细胞上表达。ICOS缺陷型MRL/lpr小鼠表现出轻度淋巴结病,脾脏中记忆型CD4(+) T细胞减少。抗双链DNA抗体水平降低。与野生型MRL/lpr小鼠相比,ICOS缺陷型MRL/lpr小鼠的CD4(+) T细胞对Th1的偏向性较小,对抗CD3抗体的反应中IL-4产生增加。虽然ICOS缺陷完全消除了肾血管炎,但肾小球肾炎的严重程度没有改变。ICOS被认为在CD4(+) T细胞活化、自身抗体产生和肾血管炎中起作用。然而,它在肾小球肾炎的发展中并非必不可少。