Expanded Double Negative T Cells in Patients with Systemic Lupus Erythematosus Produce IL-17 and Infiltrate the Kidneys

被引:603
|
作者
Crispin, Jose C. [1 ]
Oukka, Mohamed [2 ]
Bayliss, George [1 ]
Cohen, Robert A. [1 ]
Van Beek, Christine A. [3 ]
Stillman, Isaac E. [3 ]
Kyttaris, Vasileios C. [1 ]
Juang, Yuang-Taung [1 ]
Tsokos, George C. [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ctr Neurol Dis, Cambridge, MA 02139 USA
[3] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02115 USA
来源
JOURNAL OF IMMUNOLOGY | 2008年 / 181卷 / 12期
基金
美国国家卫生研究院;
关键词
D O I
10.4049/jimmunol.181.12.8761
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Double negative (DN) T cells are expanded in patients with systemic lupus erythematosus (SLE) and stimulate autoantibody production as efficiently as CD4(+) T cells. In this study, we demonstrate that DN T cells from patients with SLE produce significant amounts of IL-17 and IFN-gamma, and expand when stimulated in vitro with an anti-CD3 Ab in the presence of accessory cells. Furthermore, IL-17(+) and DN T cells are found in kidney biopsies of patients with lupus nephritis. Our findings establish that DN T cells produce the inflammatory cytokines IL-17 and IFN-gamma, and suggest that they contribute to the pathogenesis of kidney damage in patients with SLE. The Journal of Immunology, 2008, 181: 8761-8766.
引用
收藏
页码:8761 / 8766
页数:6
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