Pimecrolimus Enhances TLR2/6-Induced Expression of Antimicrobial Peptides in Keratinocytes
被引:50
作者:
Buechau, Amanda S.
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Univ Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
VA San Diego Healthcare Syst, San Diego, CA USAUniv Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
Buechau, Amanda S.
[1
,2
]
Schauber, Juergen
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Univ Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
VA San Diego Healthcare Syst, San Diego, CA USAUniv Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
Schauber, Juergen
[1
,2
]
Hultsch, Thomas
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机构:
Nova Pharmaceut Corp, E Hanover, NJ USAUniv Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
Hultsch, Thomas
[3
]
Stuetz, Anton
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Novartis Inst BioMed Res, Vienna, AustriaUniv Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
Stuetz, Anton
[4
]
Gallo, Richard L.
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Univ Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
VA San Diego Healthcare Syst, San Diego, CA USAUniv Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
Gallo, Richard L.
[1
,2
]
机构:
[1] Univ Calif San Diego, Dept Med, Div Dermatol, La Jolla, CA 92161 USA
[2] VA San Diego Healthcare Syst, San Diego, CA USA
Calcineurin inhibitors are potent inhibitors of T-cell-receptor mediated activation of the adaptive immune system. The effects of this class of drug on the innate immune response system are not known. Keratinocytes are essential to innate immunity in skin and rely on toll-like receptors (TLRs) and antimicrobial peptides to appropriately recognize and respond to injury or microbes. In this study we examined the response of cultured human keratinocytes to pimecrolimus. We observed that pimecrolimus enhances distinct expression of cathelicidin, CD14, and human beta-defensin-2 and beta-defensin-3 in response to TLR2/6 ligands. Some of these responses were further enhanced by 1,25 vitamin D3. Pimecrolimus also increased the functional capacity of keratinocytes to inhibit growth of Staphylococcus aureus and decreased TLR2/6-induced expression of IL-10 and IL-1 beta. Furthermore, pimecrolimus inhibited nuclear translocation of NFAT and NF-kappa B in keratinocytes. These observations uncover a previously unreported function for pimecrolimus in cutaneous innate host defense.