Genetic tagging shows increased frequency and longevity of antigen-presenting, skin-derived dendritic cells in vivo

被引:0
作者
Sanjay Garg
Alp Oran
Janine Wajchman
Shin Sasaki
Charles H Maris
Judith A Kapp
Joshy Jacob
机构
[1] Vaccine Research Center,Department of Microbiology and Immunology
[2] Yerkes National Primate Research Center,Department of Ophthalmology
[3] Emory University,Department of Bioregulation
[4] Emory University,undefined
[5] Leprosy Research Center,undefined
[6] National Institute of Infectious Diseases,undefined
[7] 4-2-1 Aoba-cho,undefined
[8] Higashimurayama,undefined
来源
Nature Immunology | 2003年 / 4卷
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摘要
Dendritic cells (DCs) are key regulators of immune responses that activate naive antigen-specific T lymphocytes. In draining lymph nodes, antigen-bearing DCs are reported to be rare and short-lived. How such small numbers of short-lived DCs can activate rare antigen-specific T cells is unclear. Here we show that after immunization of mouse skins by gene gun, the number of antigen-bearing DCs that migrate to draining lymph node is 100-fold higher than previously estimated and that they persist for approximately 2 weeks. The substantial frequency and longevity of DCs in situ ensures ample antigen presentation and stimulation for the rare antigen-specific T cells in draining lymph nodes.
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页码:907 / 912
页数:5
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