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Dermatology

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IL-10 is critical for Th2 responses in a murine model of allergic dermatitis
Dhafer Laouini, … , Erdyni Tsitsikov, Raif S. Geha
Dhafer Laouini, … , Erdyni Tsitsikov, Raif S. Geha
Published October 1, 2003
Citation Information: J Clin Invest. 2003;112(7):1058-1066. https://doi.org/10.1172/JCI18246.
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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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Injection of genetically engineered fibroblasts corrects regenerated human epidermolysis bullosa skin tissue
Susana Ortiz-Urda, … , M. Peter Marinkovich, Paul A. Khavari
Susana Ortiz-Urda, … , M. Peter Marinkovich, Paul A. Khavari
Published January 15, 2003
Citation Information: J Clin Invest. 2003;111(2):251-255. https://doi.org/10.1172/JCI17193.
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Injection of genetically engineered fibroblasts corrects regenerated human epidermolysis bullosa skin tissue

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Abstract

Current therapeutic strategies for genetic skin disorders rely on the complex process of grafting genetically engineered tissue to recipient wound beds. Because fibroblasts synthesize and secrete extracellular matrix, we explored their utility in recessive dystrophic epidermolysis bullosa (RDEB), a blistering disease due to defective extracellular type VII collagen. Intradermal injection of RDEB fibroblasts overexpressing type VII collagen into intact RDEB skin stably restored correctly localized type VII collagen expression in vivo and normalized hallmark RDEB disease features, including subepidermal blistering and anchoring fibril defects.

Authors

Susana Ortiz-Urda, Qun Lin, Cheryl L. Green, Douglas R. Keene, M. Peter Marinkovich, Paul A. Khavari

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Allergen-specific CD8+ T cells and atopic disease
Suranjith L. Seneviratne, … , Andrew J. McMichael, Graham S. Ogg
Suranjith L. Seneviratne, … , Andrew J. McMichael, Graham S. Ogg
Published November 1, 2002
Citation Information: J Clin Invest. 2002;110(9):1283-1291. https://doi.org/10.1172/JCI15753.
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Allergen-specific CD8+ T cells and atopic disease

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Abstract

Research Article

Authors

Suranjith L. Seneviratne, Louise Jones, Abigail S. King, Antony Black, Sheila Powell, Andrew J. McMichael, Graham S. Ogg

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The “skin”ny on epidermal RAC1 in psoriasis pathogenesis
Mårten C.G. Winge and colleagues characterize the role of RAC1 in the autoimmune disorder, psoriasis…
Published June 13, 2016
Scientific Show StopperDermatology
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