Repeated epicutaneous exposures to ovalbumin progressively induce atopic dermatitis-like skin lesions in mice
Article first published online: 28 NOV 2006
Clinical & Experimental Allergy
Volume 37, Issue 1, pages 151–161, January 2007
How to Cite
Wang, G., Savinko, T., Wolff, H., Dieu-Nosjean, M. C., Kemeny, L., Homey, B., Lauerma, A. I. and Alenius, H. (2007), Repeated epicutaneous exposures to ovalbumin progressively induce atopic dermatitis-like skin lesions in mice. Clinical & Experimental Allergy, 37: 151–161. doi: 10.1111/j.1365-2222.2006.02621.x
- Issue published online: 28 NOV 2006
- Article first published online: 28 NOV 2006
- Submitted 11 December 2005; revised 31 August 2006; accepted 19 September 2006
- animal model;
- atopic dermatitis;
- chemokine receptors;
Background Atopic dermatitis (AD) is a chronic skin disease in which environmental factors play a great role. A widely used murine model for AD has provided a useful tool to study the disease.
Objective The purpose of this study is to investigate kinetically the induction of this AD model and the processes involved in the development of AD due to extrinsic allergen exposures.
Methods BALB/c mice were epicutaneously exposed to ovalbumin (OVA) for 3 weeks; each week was separated by a 2-week resting period. Mice were killed after each exposure week. Skin biopsies and blood were obtained for histological study, RNA isolation and antibody analysis.
Results There was a progressive and significant thickening of the epidermis and dermis in OVA-exposed mice. Significantly increased dermal cell infiltration of eosinophils, mast cells and total inflammatory cells, including CD3 and CD4 cells, was found after each OVA exposure week. Total IgE, IgG2a and OVA-specific IgE were significantly increased after the second and third exposure week, while OVA-specific IgG2a was significantly induced after the third exposure week. Gradual and/or significant increases in mRNA expression of IL-1β, TNF-α, IL-4, IL-10, IL-13, IFN-γ and IL-12p35 were found after each exposure week. Chemokines and their receptors involved in both T-helper type 1 (Th1)- and Th2-type cell recruitment (CCL1, CCL8, CCL11, CCL24, CXCL9, CXCL10, CCR1, CCR3, CCR5, CCR8 and CXCR3) were up-regulated significantly at different time-points.
Conclusion This study provides an insight into the dynamic nature and time-dependent transition of skin inflammation and systemic immune responses in a murine AD model induced by repeated epicutaneous exposures to OVA.