Effects of a PEGylated soluble TNF receptor type 1 (PEG sTNF-RI) on cytokine expression in adjuvant arthritis

被引:8
作者
Bush, KA
Walker, JS
Frazier, J
Kirkham, BW
机构
[1] Guys & St Thomas Hosp, Dept Rheumatol, London SE1 9RT, England
[2] Univ New S Wales, Sch Physiol & Pharmacol, Sydney, NSW, Australia
关键词
adjuvant arthritis; cytokines; synovium; TNF-blockade;
D O I
10.1080/030097402320318378
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To investigate the effects of TNF blocking therapy on synovial immune activity in rat adjuvant arthritis (AA) by measuring mRNA expression of key macrophage and T cell cytokines during PEG sTNF-RI treatment (10 mg/kg) on days 8, 10 and 12. Methods: Paw volume was assessed every 3-4 days. Ankles were removed for quantitative radiology and histology and synovial membrane removed to determine cytokine mRNA expression using semi-quantitative RT-PCR. T cells in joints were quantified by immunohistochemistry. Results: Paw volume was significantly decreased in rats treated with PEG STNF-RI from days 12 to 17. Histology scores and synovial T cell numbers were reduced on days 13 and 17 and radiology scores significantly reduced on day 13. Expression of synovial TNF, IFN-gamma, IL-17, IL-2 and IL-4 mRNA was unchanged in treated rats and TGF-beta expression was significantly increased at day 13. Conclusions: PEG sTNF-RI attenuates AA and disease recurs after treatment ceases, similar to human rheumatoid arthritis. Continued TNF production and/or ongoing T cell activity, may explain the recrudescence of disease once treatment is stopped.
引用
收藏
页码:198 / 204
页数:7
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