Guest guest Posted September 11, 2007 Report Share Posted September 11, 2007 Dear All; I've been boring you all lately with discussion of pro-inflammatory Th17 cells, which produce a potent set of pro-inflammatory cytokines like interleukin-17 (IL-17). These cells are now being looked at closely in many autoimmune diseases, and I have been strongly hinting that these cells should be examined carefully in ulcerative colitis and PSC! Here's an interesting recent paper which points to the importance of interleukin-17 in ulcerative colits, and in particular pancolits [the type often found in PSC]. J. Clin. Immunol. 2007 Sep 9; [Epub ahead of print] The Influence of Polymorphisms of Interleukin-17A and Interleukin-17F Genes on the Susceptibility to Ulcerative Colitis. Arisawa T, Tahara T, Shibata T, Nagasaka M, Nakamura M, Kamiya Y, Fujita H, Nakamura M, Yoshioka D, Arima Y, Okubo M, Hirata I, Nakano H. Department of Gastroenterology, Fujita Health University School of Medicine, 1-98, Dengakugakubo, Kutsukake-cho, Toyoake, 470-1192, Japan, tarisawa@.... We investigated the association between ulcerative colitis (UC) and polymorphisms of IL-17A (rs2275913, G-197A) and IL-17F (rs763780, 7488T/C) genes. We employed the multiplex PCR-SSCP method to detect gene polymorphisms. Both the numbers of -197A (IL-17A) and 7488T (IL- 17F) alleles were significantly correlated to the development of UC. The frequencies of -197A/A and 7488T/T genotypes in the UC group were significantly higher than those in the non-UC group. An adjusted analysis revealed that -197A and 7488T alleles were independent risk factors for the developing UC. In addition, both polymorphisms were significantly associated with the pancolitis phenotype. Furthermore, - 197A allele was significantly correlated to the chronic relapsing phenotype and -197A/A homozygote was more frequent in steroid- dependent cases, whereas 7488T allele was correlated with the chronic continuous phenotype. Our results provided the first evidence that - 197A (IL-17A) and 7488T (IL-17F) alleles may influence the susceptibility to and pathophysiological features of UC independently. PMID: 17828618. __________________ On a totally different subject, I'd like to report to the group that Ricky Safer and I recently submitted a grant proposal on behalf of PSC Partners Seeking a Cure, to Cordis Corporation (a division of & ) for an educational grant .... a grant to fund the PSC Partners Seeking a Cure and PSC Literature web sites, and enhancements to them, over the next 3 years. Ricky and I are very pleased to announce that Cordis Corporation plans to give us $9,000 for this effort. Thank you so much Cordis Corporation! Dave (father of (22); PSC 07/03; UC 08/03) Quote Link to comment Share on other sites More sharing options...
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