Increased antigen presenting cell-mediated T cell activation in mice and patients without the autoimmune regulator

被引:65
作者
Ramsey, C
Hässler, S
Marits, P
Kämpe, O
Surh, CA
Peltonen, L
Winqvist, O
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA USA
[2] Univ Uppsala Hosp, Dept Med Sci, Uppsala, Sweden
[3] Karolinska Inst, Dept Med, Unit Clin Allergy Res, Stockholm, Sweden
[4] Natl Publ Hlth Inst, Dept Human Mol Genet, Helsinki, Finland
[5] Univ Helsinki, Dept Med Genet, Helsinki, Finland
关键词
antigen-presenting cell; autoimmunity; clinical immunology; knockout mice; microarray;
D O I
10.1002/eji.200535240
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients with autoimmune polyendocrine syndrome type I (APS I) suffer from endocrine and non-endocrine disorders due to mutations in the autoimmune regulator gene (AIRE). Mouse Aire is expressed both in thymic medullary epithelial cells and in peripheral antigen-presenting cells, suggesting a role in both central and peripheral tolerance. We here report that Aire(-/-) dendritic cells (DC) activate naive T cells more efficiently than do Aire(+/+) DC. Expression array analyses of Aire(-/-) DC revealed differential regulation of 68 transcripts, among which, the vascular cell adhesion molecule-1 (VCAM-1) transcript was up-regulated in Aire(-/-) DC. Concurrently, the expression of the VCAM-1 protein was up-regulated on both Aire(-/-) DC and monocytes from APS I patients. Blocking the interaction of VCAM-1 prevented enhanced Aire(-/-) DC stimulation of T cell hybridomas. We determined an increased number of DC in spleen and lymph nodes and of monocytes in the blood from Aire(-/-) mice, and an increased number of blood monocytes in APS I patients. Our findings imply a role for Aire in peripheral DC regulation of T cell activation, and suggest that Aire participates in peripheral tolerance.
引用
收藏
页码:305 / 317
页数:13
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