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pubmed-article:11850721pubmed:abstractTextBiological effects of in vivo transfection of a potential anti-inflammatory gene, designated Sm16, cloned from the human parasite Schistosoma mansoni were analyzed in these studies. A single intradermal injection of a full-length cDNA of Sm16 resulted in the expression of Sm16 in the epidermis, dermis, skin migratory cells and skin-draining lymph nodes of mice for up to 7 days. Subsequently the anti-inflammatory effect of this gene expression was evaluated by inducing an inflammatory response in the skin of mice. These studies showed that Sm16 gene delivery resulted in a significant suppression of cutaneous inflammation as shown by a reduction in cutaneous edema, decrease in neutrophil infiltration, suppression of pro-inflammatory cytokine expression and down-regulation of ICAM-1 expression in the skin inflammatory site. Cells collected from the skin-draining lymph nodes showed reduced proliferation to mitogen. Multiple intradermal injection of Sm16 cDNA failed to induce any antibody response in mice for up to 8 weeks after initial injection. These findings suggest a potential for developing Sm16 gene delivery as a therapeutic agent for treating inflammatory skin disorders.lld:pubmed
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pubmed-article:11850721pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:11850721pubmed:year2002lld:pubmed
pubmed-article:11850721pubmed:articleTitleSuppression of cutaneous inflammation by intradermal gene delivery.lld:pubmed
pubmed-article:11850721pubmed:affiliationDepartment of Biomedical Sciences, College of Medicine, University of Illinois, Rockford, IL 61107, USA.lld:pubmed
pubmed-article:11850721pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11850721pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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