Monocytes from Patients with Type 1 Diabetes Spontaneously Secrete Proinflammatory Cytokines Inducing Th17 Cells

被引:220
作者
Bradshaw, Elizabeth M. [1 ]
Raddassi, Khadir [1 ]
Elyaman, Wassim [1 ]
Orban, Tihamer [2 ]
Gottlieb, Peter A. [3 ]
Kent, Sally C. [1 ]
Hafler, David A. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Mol Immunol,Ctr Neurol Dis, Boston, MA 02115 USA
[2] Harvard Univ, Joslin Diabet Ctr, Sch Med, Sect Immunol & Immunogenet, Boston, MA 02215 USA
[3] Univ Colorado, Barbara Davis Ctr Childhood Diabet, Denver & Hlth Sci Ctr, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
GROWTH-FACTOR-BETA; BLOOD MONONUCLEAR-CELLS; AUTOIMMUNE INFLAMMATION; GENE-EXPRESSION; RECEPTOR (TLR)2; T-CELLS; DIFFERENTIATION; INTERLEUKIN-23; INDUCTION; CHILDREN;
D O I
10.4049/jimmunol.0900576
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoimmune diseases including type 1 diabetes (T1D) are thought to have a Th1/Th17 bias. The underlying mechanisms driving the activation and differentiation of these proinflammatory T cells are unknown. We examined the monocytes isolated directly from the blood of T1D patients and found they spontaneously secreted the proinflammatory cytokines IL-1 beta and IL-6, which are known to induce and expand Th17 cells. Moreover, these in vivo-activated monocytes from T1D subjects induced more IL-17-secreting cells from memory T cells compared with monocytes from healthy control subjects. The induction of IL-17-secreting T cells by monocytes from T1D subjects was reduced in vitro with a combination of an IL-6-blocking Ab and IL-1R antagonist. In this study, we report a significant although modest increase in the frequency of IL-17-secreting cells in lymphocytes from long-term patients with T1D compared with healthy controls. These data suggest that the innate immune system in T1D may drive the adaptive immune system by expanding the Th17 population of effector T cells. The Journal of Immunology, 2009,183: 4432-4439.
引用
收藏
页码:4432 / 4439
页数:8
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