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Vol. 288, Issue 1, 43-50, January 1999
Department of Pharmacology, Gifu Pharmaceutical University, Gifu,
Japan (H.N., Y.U., H.T., Y.H., N.N., N.I.);
Institute of Medical
Science, University of Tokyo, Tokyo, Japan (K.T.); and
Gifu College of
Medical Technology, Seki, Japan (K.K.)
The effect of overproduction of interleukin (IL) 5 on the allergic
cutaneous response was investigated in transgenic mice overexpressing
IL-5. Five repeated topical applications of 2,4-dinitrofluorobenzene (DNFB) to the ears of mice resulted in allergic dermatitis on the ears
as well as significant elevation in dinitrophenol-specific IgE antibody
and total IgE in the serum in both wild-type and transgenic
mice. The development of dermatitis as measured by skin thickness and
histopathological changes were potentiated in the transgenic mice. In
IL-5 transgenic mice, significant accumulation of eosinophils in skin
lesions was observed after five paintings of DNFB, and the magnitudes
of eosinophilia and IL-5 messenger RNA expression were significantly
higher than in wild-type mice. The dinitrophenol-specific and total IgE
in the serum were higher in IL-5 transgenic mice. The late phase
reaction of IgE antibody-mediated biphasic cutaneous response was
potentiated in IL-5 transgenic mice. The magnitudes of vasopermeability
increase by passive cutaneous anaphylaxis, serotonin, and
platelet-activating factor were similar in both mice. These results
indicate that overproduction of IL-5 resulted in the potentiation of
DNFB-induced dermatitis by elevation of IgE production, IgE-mediated
allergic late-phase cutaneous reaction, and eosinophilia in the skin lesion.
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