Epidermal T Cells and Wound Healing

被引:141
作者
Havran, Wendy L. [1 ]
Jameson, Julie M. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
KERATINOCYTE GROWTH FACTOR-2; DEXTRAN SULFATE SODIUM; INFLAMMATORY RESPONSE; HUMAN-SKIN; EPITHELIAL-CELLS; AIRWAY HYPERREACTIVITY; GENE REARRANGEMENT; VIRUS-INFECTION; LYMPHOCYTES; RECEPTOR;
D O I
10.4049/jimmunol.0902733
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The murine epidermis contains resident T cells that express a canonical gamma delta TCR. These cells arise from fetal thymic precursors and use a TCR that is restricted to the skin in adult animals. These cells assume a dendritic morphology, in normal skin and constitutively produce low levels of cytokines that contribute to epidermal homeostasis. When skin is wounded, an unknown Ag is expressed on damaged keratinocytes. Neighboring gamma delta T cells then round up and contribute to wound healing by local production of epithelial growth factors and inflammatory cytokines. In the absence of skin gamma delta T cells, wound healing is impaired. Similarly, epidermal T cells from patients with healing wounds are activated and secreting growth factors. Patients with nonhealing wounds have a defective epidermal T cell response. Information gained on the role of epidermal-resident T cells in the mouse may provide information for development of new therapeutic approaches to wound healing. The Journal of Immunology, 2010, 184: 5423-5428.
引用
收藏
页码:5423 / 5428
页数:6
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