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雷公藤多苷对寻常性银屑病患者血清中白细胞介素-6、17及23水平的影响 被引量:11

Effect of Tripterygium wilfordii on serum levels of IL-6, IL-17 and IL-23 in patients with psoriasis vulgaris
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摘要 目的:观察雷公藤多苷治疗寻常性银屑病的疗效,并检测其对患者血清中白细胞介素(IL)-6、IL-17及IL-23水平的影响,探讨雷公藤多苷治疗寻常性银屑病的作用机制。方法:采用酶联免疫吸附试验(ELISA)法检测40例寻常性银屑病患者经雷公藤多苷治疗前后血清中IL-6、IL-17及IL-23水平变化。结果:雷公藤多苷治疗寻常性银屑病8周后银屑病皮损面积及严重度指数(PASI)评分显著下降(P<0.01)。患者血清中IL-6、IL-17及IL-23水平治疗前分别为(184.16±26.19)ng/L、(7.43±2.02)ng/L和(1622.44±254.56)ng/L,治疗后分别为(136.03±16.19)ng/L、(3.07±0.67)ng/L和(824.72±141.54)ng/L,治疗前后比较,差异有统计学意义(P均<0.01),IL-17、IL-23与PASI评分呈正相关。结论:雷公藤多苷治疗寻常性银屑病疗效显著,可能通过调节Th17细胞降低血清中IL-6、IL-17及IL-23的水平发挥作用。 Objective: To evaluate the efficacy of Tripterygium wilfordii for psoriasis vulgaris, and its effect on serum levels of IL-6, IL-17 and IL-23. Methods: ELISA assay was used to measure serum levels of IL-6, IL-17 and IL-23 in 40 pa- tients with psoriasis vulgaris before and after Tripterygium wilfordii treatment. Thirty eight normal subjects served as controls. Results: Treatments with Tripterygium wilfordii for 8 weeks lowered the PASI scores significantly(P〈0.01). In addition, treat- ments with Tripterygium wilfordii also markedly reduced serum levels of IL-6, IL-17 and IL-23(IL-6:184.16±26.19 ng/L vs. 136.03±16.19 ng/L; IL-17:7.43±2.02 ng/L vs. 3.07±0.67 ng/L; IL-23:1622.44±254.56 ng/L vs. 824.72±141.54. P〈0.01 for all). Both IL-17 and IL-23 levels positively correlated with PASI scores. Conclusions: Tripterygium wilfordii is effective for psoriasis vulgaris, possibly by regulating Thl7 cells, leading to reductions in serum IL-6, IL-17 and IL-23.
出处 《临床皮肤科杂志》 CSCD 北大核心 2017年第12期877-879,共3页 Journal of Clinical Dermatology
关键词 银屑病 寻常性 雷公藤多苷 IL-6 IL-17 IL-23 psoriasis vulgaris Tripterygium wilfordii IL-6 IL-17 IL-23
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  • 1李家文,吴艳,李东升,谭志建.β趋化因子CCL20及其受体CCR6 mRNA在寻常性银屑病患者皮损中的表达[J].临床皮肤科杂志,2004,33(9):532-534. 被引量:5
  • 2李常兴,张锡宝,黄振明,刘玉梅,吴志华,陈秋霞.甲氨蝶呤治疗中、重度银屑病的疗效观察[J].临床皮肤科杂志,2006,35(5):327-328. 被引量:30
  • 3Williams IR. CCR6 and CCL20: partners in intestinal immunity and lymphorganogenesis[J]. Ann N Y Acad Sci, 2006, 1072(1): 52-61.
  • 4Schutyser E, Struyf S, Van Damme J. The CC chemokine CCL20 and its receptor CCR6 [J]. Cytokine Growth Factor Rev, 2003, 14(5): 409-426.
  • 5Hirota K, Yoshitomi H, Hashimoto M, et al. Preferential recruit- ment of CCR6-expressing Thl7 cells to inflamed joints via CCL20 in rheumatoid arthritis and its animal model[J]. J Exp Med, 2007, 204(12): 2803-2812.
  • 6Ixwes MA, Kikuchit IT, Fuentes-duculan J, et al. Psoriasis vul- garis lesions contain discrete populations of Thl and Thl7 T Cells[J]. J Invest Dennatol, 2008, 128 (5): 1207-1211.
  • 7Harper EG, Guo C, Rizzo H, et al. Thl7 cytokines stimulate CCL20 expression in keratinocytes in vitro and in vivo: implica- tions for psoriasis pathogenesis[J]. J Invest Dermatol, 2009, 129(9): 2175-2183.
  • 8Homey B, Dieu-Nosjean MC, Wiesenborn A, et al.Up-Regulation of Macrophage Inflammatory Protein-3odCCL20 and CC Chemokine Receptor 6 in Psoriasis[J]. J hnmunol, 2000, 164(12): 6621-6632.
  • 9Kochi Y, Okada Y, Suzuki A, et al. A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility[J]. Nat Genet, 2010, 42(6): 515-519.
  • 10Girolomoni G, Mrowietz U, Paul C, Psoriasis: rationale for target- ing interleukin-17[J]. Br J Dermatol, 2012, 167(4): 717-724.

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