The role of IL-23/IL-17 axis in lupus nephritis.

The role of IL-23/IL-17 axis in lupus nephritis.
复制标题

DOI:
10.4049/jimmunol.0900385
复制
发表时间:
2009-09-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
通讯作者:
Tsokos GC
Tsokos GC
中科院分区:
其他
文献类型:
--
作者:
Zhang Z;Kyttaris VC;Tsokos GC

文献摘要

参考文献

被引文献

相似文献

表达IL-17的T细胞浸润系统性红斑狼疮患者的肾脏。这些细胞中有很大一部分是CD 3 + CD 4 − CD 8 −双阴性T细胞。在这项研究中,我们表明,从MRL/lpr小鼠的双阴性T细胞表达大量的IL-17,并作为疾病进行性恶化,IL-17和IL-23受体在淋巴细胞从这些小鼠的表达增加。来自狼疮易感小鼠的淋巴结细胞,而不是对照小鼠,在体外用IL-23处理,当转移到非自身免疫性、淋巴细胞缺陷型Rag-1−/−小鼠时,诱导肾炎。来自这些受体小鼠的肾脏标本显示显著的IG和补体沉积。这些数据表明,异常活跃的IL-23/IL-17轴有助于狼疮易感小鼠肾炎的发展。
T cells that express IL-17 infiltrate the kidneys of patients with systemic lupus erythematosus. A significant proportion of these cells are CD3+CD4−CD8− double-negative T cells. In this study, we show that double-negative T cells from MRL/lpr mice express high amounts of IL-17 and that as disease progressively worsens, the expression of IL-17 and of IL-23 receptor in lymphocytes from these mice increases. Lymph node cells from lupus-prone mice, but not control mice, treated in vitro with IL-23 induce nephritis when transferred to non-autoimmune, lymphocyte-deficient Rag-1−/− mice. Kidney specimens from these recipient mice show significant Ig and complement deposition. The data indicate that an aberrantly active IL-23/IL-17 axis contributes to the development of nephritis in lupus-prone mice.
DOI: 10.4049/jimmunol.170.7.3915
发表时间: 2003-04-01
影响因子: 4.4
作者:
Kikawada, E;Lenda, DM;Kelley, VR
通讯作者: Kelley, VR
DOI: 10.1177/0961203308090029
发表时间: 2008-01-01
期刊: LUPUS
影响因子: 2.6
作者:
Houssiau, F. A.;Ginzler, E. M.
通讯作者: Ginzler, E. M.
DOI: 10.1182/blood-2005-09-010116
发表时间: 2007-05-01
期刊: BLOOD
影响因子: 20.3
作者:
Yu, Jeffrey J.;Ruddy, Matthew J.;Gaffen, Sarah L.
通讯作者: Gaffen, Sarah L.
DOI: 10.1191/0961203305lu2055oa
发表时间: 2005-01-01
期刊: LUPUS
影响因子: 2.6
作者:
Balow, JE
通讯作者: Balow, JE