Density of CD163+CD11c+ Dendritic Cells Increases and CD103+ Dendritic Cells Decreases in the Coeliac Lesion

被引:34
作者
Beitnes, A. -C. R. [1 ]
Raki, M. [1 ]
Lundin, K. E. A. [1 ,2 ]
Jahnsen, J. [3 ]
Sollid, L. M. [1 ,4 ]
Jahnsen, F. L. [5 ]
机构
[1] Oslo Univ Hosp, Rikshosp, Ctr Immune Regulat, Inst Immunol, N-0424 Oslo, Norway
[2] Oslo Univ Hosp, Rikshosp, Dept Med, N-0424 Oslo, Norway
[3] Oslo Univ Hosp, Rikshosp, Dept Gastroenterol, N-0424 Oslo, Norway
[4] Univ Oslo, Rikshosp, Ctr Immune Regulat, Inst Immunol, N-0027 Oslo, Norway
[5] Oslo Univ Hosp, Rikshosp, Ctr Immune Regulat, Dept Pathol, N-0424 Oslo, Norway
关键词
INTESTINAL LAMINA PROPRIA; T-CELLS; HUMAN-MONOCYTES; DISEASE; MACROPHAGES; ANTIGEN; DIFFERENTIATION; PATHOLOGISTS; STIMULATION; PHENOTYPE;
D O I
10.1111/j.1365-3083.2011.02549.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Coeliac disease is a chronic inflammation of the intestinal mucosa controlled by gluten-specific T cells restricted by disease-associated HLA-DQ molecules. We have previously reported that mucosal CD11c(+) dendritic cells (DCs) are responsible for activation of gluten-reactive T cells within the coeliac lesion. In mice, intestinal CD11c(+) DCs comprise several functionally distinct subsets. Here, we report that HLA-DQ(+) antigen-presenting cells (APCs) in normal human duodenal mucosa can be divided into four subsets with striking similarities to those described in mice: CD163(+)CD11c(-) macrophages (74%), and CD11c(+) cells expressing either CD163 (7%), CD103 (11%) or CD1c (13%). CD103(+) and CD1c(+) DCs belonged to partly overlapping populations, whereas CD163(+)CD11c(+) APCs appeared to be a distinct population. In the coeliac lesion, we found increased density of CD163(+)CD11c(+) APCs, whereas the density of CD103(+) and CD1c(+) DCs was decreased, suggesting that distinct subpopulations of APCs in coeliac disease may exert different functions in the pathogenesis.
引用
收藏
页码:186 / 194
页数:9
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