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IL-10 is critical for Th2 responses in a murine model of allergic dermatitis
Dhafer Laouini, Harri Alenius, Paul Bryce, Hans Oettgen, Erdyni Tsitsikov, Raif S. Geha
Dhafer Laouini, Harri Alenius, Paul Bryce, Hans Oettgen, Erdyni Tsitsikov, Raif S. Geha
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Article Dermatology

IL-10 is critical for Th2 responses in a murine model of allergic dermatitis

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Abstract

We found that mechanical injury to mouse skin, which can be caused by tape stripping, results in rapid induction of IL-10 mRNA. IL-10–/– mice were used to examine the role of IL-10 in a mouse model of allergic dermatitis induced by epicutaneous (EC) sensitization with OVA on tape-stripped skin. Skin infiltration by eosinophils and expression of eotaxin, IL-4, and IL-5 mRNA in OVA-sensitized skin sites were severely diminished in IL-10–/– mice. Following in vitro stimulation with OVA, splenocytes from EC-sensitized IL-10–/– mice secreted significantly less IL-4, but significantly more IFN-γ, than splenocytes from WT controls. A similar skewing in cytokine secretion profile was observed in the splenocytes of IL-10–/– mice immunized intraperitoneally with OVA. IL-10–/– APCs skewed the in vitro response of OVA T cell receptor (TCR) transgenic T cells towards Th1. Examination of the Th response of WT and IL-10–/– mice immunized with OVA-pulsed WT or IL-10–/– DCs revealed that both DCs and T cells participate in IL-10 skewing of the Th2 response in vivo. These results suggest that IL-10 plays an important role in the Th2 response to antigen and in the development of skin eosinophilia in a murine model of allergic dermatitis.

Authors

Dhafer Laouini, Harri Alenius, Paul Bryce, Hans Oettgen, Erdyni Tsitsikov, Raif S. Geha

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Figure 1

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IL-10 mRNA expression in skin of C57BL/6 mice following tape stripping s...
IL-10 mRNA expression in skin of C57BL/6 mice following tape stripping six times. (a) Results of a representative experiment. pMUS plasmid and cDNA were coamplified by Taq polymerase generating 300-bp PCR fragments from the pMUS plasmid and 252-bp fragments from IL-10 cDNA. In parallel, pMUS plasmid and cDNA samples were coamplified for β2m cDNA. The samples were run on 1.6% agarose gel and stained with ethidium bromide. (b) Pooled results of experiments using six mice. Cytokine transcripts were quantitated by RT-PCR and expressed as fg per 10 pg of β2m mRNA. Columns and error bars represent mean ± SEM.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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