Myeloperoxidase Inhibition Ameliorates Plaque Psoriasis in Mice

被引:17
作者
Neu, Savannah D. [1 ,2 ]
Strzepa, Anna [1 ,3 ]
Martin, Dustin [4 ]
Sorci-Thomas, Mary G. [5 ]
Pritchard, Kirkwood A., Jr. [4 ]
Dittel, Bonnie N. [1 ]
机构
[1] Versiti Blood Res Inst, Milwaukee, WI 53201 USA
[2] Med Coll Wisconsin, Dept Microbiol & Immunol, Milwaukee, WI 53226 USA
[3] Jagiellonian Univ Med Coll, Dept Med Biol, PL-31034 Krakow, Poland
[4] Med Coll Wisconsin, Dept Surg, Div Pediat Surg, Milwaukee, WI 53226 USA
[5] Med Coll Wisconsin, Dept Med, Div Endocrinol & Mol Med, Milwaukee, WI 53226 USA
基金
美国国家卫生研究院;
关键词
plaque psoriasis; myeloperoxidase; neutrophils; Imiquimod; Aldara; psoriasis area and severity index (PASI); N-acetyl lysyltyrosylcysteine amide (KYC); TOPICAL TREATMENT; MONOCLONAL-ANTIBODY; SKIN INFLAMMATION; OXIDATIVE STRESS; DENDRITIC CELLS; DOUBLE-BLIND; T-CELL; DISEASE; KERATINOCYTES; EXPRESSION;
D O I
10.3390/antiox10091338
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plaque psoriasis is a common inflammatory condition of the skin characterized by red, flaking lesions. Current therapies for plaque psoriasis target many facets of the autoimmune response, but there is an incomplete understanding of how oxidative damage produced by enzymes such as myeloperoxidase contributes to skin pathology. In this study, we used the Aldara (Imiquimod) cream model of plaque psoriasis in mice to assess myeloperoxidase inhibition for treating psoriatic skin lesions. To assess skin inflammation severity, an innovative mouse psoriasis scoring system was developed. We found that myeloperoxidase inhibition ameliorated psoriasis severity when administered either systemically or topically. The findings of this study support the role of oxidative damage in plaque psoriasis pathology and present potential new therapeutic avenues for further exploration.
引用
收藏
页数:15
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