Staphylococcus aureus Lipoprotein Induces Skin Inflammation, Accompanied with IFN--Producing T Cell Accumulation through Dermal Dendritic Cells

被引:14
作者
Saito, Suguru [1 ,2 ]
Quadery, Ali F. [3 ]
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Kidney Res Ctr, Div Clin Nephrol & Rheumatol, Niigata 9518510, Japan
[2] Acad Sinica, Inst Bio Med Sci, Taipei 115, Taiwan
[3] Niigata Univ, Biofluid Biomarker Ctr, Niigata 9502181, Japan
关键词
S; aureus; lipoprotein; skin inflammation; dendritic cell; effector T cell; ATOPIC-DERMATITIS; LANGERHANS CELLS; ADAPTIVE IMMUNITY; WALL COMPONENTS; TEICHOIC-ACIDS; MAST-CELLS; RECEPTOR; DISEASE; PEPTIDOGLYCAN; RECOGNITION;
D O I
10.3390/pathogens7030064
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus aureus (S. aureus) is a commensal bacteria on the human skin, which causes serious skin inflammation. Several immune cells, especially effector T cells (Teff), have been identified as key players in S. aureus-derived skin inflammation. However, the bacterial component that induces dramatic host immune responses on the skin has not been well characterized. Here, we report that S. aureus lipoprotein (SA-LP) was recognized by the host immune system as a strong antigen, so this response induced severe skin inflammation. SA-LP activated dendritic cells (DCs), and this activation led to Teff accumulation on the inflamed skin in the murine intradermal (ID) injection model. The skin-accumulated Teff pool was established by IFN-?-producing CD4(+) and CD8(+)T (Th1 and Tc1). SA-LP activated dermal DC (DDC) in a dominant manner, so that these DCs were presumed to possess the strong responsibility of SA-LP-specific Teff generation in the skin-draining lymph nodes (dLN). SA-LP activated DC transfer into the mice ear, which showed similar inflammation, accompanied with Th1 and Tc1 accumulation on the skin. Thus, we revealed that SA-LP has a strong potential ability to establish skin inflammation through the DC-Teff axis. This finding provides novel insights not only for therapy, but also for the prevention of S. aureus-derived skin inflammation.
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页数:17
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