Treg-enriched CD4+T cells attenuate collagen synthesis in keloid fibroblasts

被引:44
|
作者
Murao, Naoki [1 ]
Seino, Ken-ichiro [2 ]
Hayashi, Toshihiko [1 ,3 ]
Ikeda, Masaki [1 ]
Funayama, Emi [1 ]
Furukawa, Hiroshi [1 ]
Yamamoto, Yuhei [1 ]
Oyama, Akihiko [1 ]
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Plast & Reconstruct Surg, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Inst Med Genet, Div Immunobiol, Sapporo, Hokkaido 0608638, Japan
[3] Hokkaido Univ, Grad Sch Dent Med, Dept Oral & Maxillofacial Surg, Sapporo, Hokkaido 0608638, Japan
关键词
coculture; fibroblast; keloid; regulatory T cell; REGULATORY T-CELLS; GENE-EXPRESSION; HYPERTROPHIC SCARS; SYSTEMIC-SCLEROSIS; I COLLAGEN; TGF-BETA; EXPANSION; PATHOPHYSIOLOGY; INTERLEUKIN-10; PATHOGENESIS;
D O I
10.1111/exd.12368
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Keloid is an inflammatory and fibrotic disease with an unknown pathogenesis. Regulatory T cells (Tregs) of CD4+ lineage can suppress other effector CD4+ T cells and modulate the immune response. A relative decrease in the number of Tregs may be involved in the pathogenesis of inflammatory and fibrotic diseases. We therefore investigated the number of Tregs in keloids using immunohistochemistry and examined the interaction between Tregs and keloid fibroblasts (KFs) using a coculture system. It was found that the ratio of Tregs/CD4+ T cells was lower compared with that in other common inflammatory skin conditions. In addition, Treg-enriched CD4+ T cells reduced collagen synthesis by KFs. Our findings suggest that a local imbalance of Tregs contributes to the development of keloids and that correction of this imbalance might represent a novel therapeutic approach to keloid fibrosis.
引用
收藏
页码:266 / 271
页数:6
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