Evaluation of FITC-Induced Atopic Dermatitis-Like Disease in NC/Nga Mice and BALB/c Mice Using Computer-Assisted Stereological Toolbox, a Computer-Aided Morphometric System

被引:6
作者
Hvid, Malene [1 ,3 ]
Jensen, Helene Kofoed [3 ]
Deleuran, Bent [2 ,3 ]
Kemp, Kaare [4 ]
Andersson, Christina [4 ]
Deleuran, Mette
Vestergaard, Christian
机构
[1] Aarhus Univ Hosp, Dept Dermatovenerol, Res Lab S, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Rheumatol, DK-8000 Aarhus, Denmark
[3] Univ Aarhus, Inst Med Microbiol & Immunol, Aarhus, Denmark
[4] LEO Pharma, Ballerup, Denmark
关键词
NC/Nga mice; Atopic dermatitis; Computer Assisted Stereological Toolbox; CD4; CD8; TOPICAL APPLICATION; EXPRESSION; OINTMENT; LESIONS; MODEL;
D O I
10.1159/000199714
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
Background: The NC/Nga mouse spontaneously develops eczematous atopic dermatitis (AD)-like skin lesions when maintained under conventional conditions, but not when kept under specific pathogen-free (SPF) conditions. Hence, there is a need for an AD model in mice housed under SPF conditions, as this is mandatory for research animals in many countries. Methods: We evaluated the use of the hapten FITC as an inducer of AD-like disease in NC/Nga and BALB/c mice maintained under SPF conditions. Mice were either untreated or treated with tacrolimus or betamethasone. Using the software Computer Assisted Stereological Toolbox as a stereological method, the mice were sensitized to FITC and the histological efficiency of disease induction with regard to inflammation and CD4+ and CD8+ lymphocytes, in addition to mast cells, was evaluated. The method was validated by comparison to a conventional semiquantitative observer-dependent method. Results: Our findings prove that FITC does indeed induce AD-like lesions in NC/Nga mice with regard to the histological appearance of the mice. However, when evaluating the immunological response in the affected areas of the mice with regard to the CD4/CD8 ratio and the effect of treatment, we found that the immune response in the NC/Nga mice differed from AD skin lesions in humans in certain aspects. Conclusions: These results emphasize the importance of an assessment of not only the histological but also the immunological appearance of the skin when evaluating AD-like disease in mice as a model for AD in humans. Copyright (c) 2009 S. Karger AG, Basel
引用
收藏
页码:188 / 194
页数:7
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