期刊文献+

β-防御素在银屑病发病机制中的作用

Beta-defensins in the pathogenesis of psoriasis
原文传递
导出
摘要 β-防御素是一组小分子抗菌肽,能够抗多种病原微生物感染,促进炎症反应,并对T细胞等发挥趋化作用。研究发现,银屑病发病可能与β-防御素有关。β-防御素可活化银屑病免疫相关的炎症因子,趋化未成熟的树突细胞和记忆T细胞,并通过促分裂素原活化蛋白激酶作用于角质形成细胞产生炎症因子,将固有性免疫和获得性免疫连接起来。未来应深入探讨β-防御素在银屑病发病中的作用,进一步完善银屑病的免疫学发病机制,寻求治疗新靶点。 Beta-defensins are a group of small-molecule antibacterial peptides, which can resist infection with various pathogenic microorganisms, promote inflammation, and act as chemoattraetants for T cells. Beta-defensins are speculated to be associated with the pathogenesis of psoriasis. They can attract immature dendritic cells and memory T cells, activate immunity-related inflammatory factors involved in psoriasis, and connect the innate and adaptive immunity via inflammatory cytokines produced by keratinocytes after stimulation by mitogen-activated protein kinases. It is warranted to assess the effects of beta-defensins in the pathogenesis of, clarify the immunological pathogenesis of, and to seek new therapeutic targets in the future for, psoriasis.
出处 《国际皮肤性病学杂志》 2012年第1期27-29,共3页 International Journal of Dermatology and Venereology
关键词 银屑病 Β防御素 MAP激酶激酶1 Psoriasis Beta defensins MAP kinase kinase 1
  • 相关文献

参考文献23

  • 1Nair RP, Stuart PE, Nistor I, et al. Sequence and haplotype analysis supports HLA-C as the psoriasis susceptibility 1 gene. Am J Hum Genet, 2006, 78(5): 827-851.
  • 2Capon F, Di Meglio P, Szaub J, et al. Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis. Hum Genet, 2007, 122(2): 201-206.
  • 3Zhang XJ, Huang W, Yang S, et al. Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. Nat Genet, 2009, 41 (2): 205-210.
  • 4Ellinghaus E, Ellinghaus D, Stuart PE, et al. Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. Nat Genet, 2010, 42(11 ): 991-995.
  • 5Sun LD, Cheng H, Wang ZX, et al. Association analyses identify six new psoriasis susceptibility loci in the Chinese population. Nat Genet, 2010, 42(11): 1005-1009.
  • 6Suzuki Y, Inokuchi S, Takazawa K, et al. Introduction of human β-defensin-3 into cultured human keratinocytes and fibroblasts by infection of a recombinant adenovirus vector. Burns, 2011, 37 (1): 109-116.
  • 7Winter J, Pantelis A, Reich R, et al. Human beta-defensin-1, -2, and -3 exhibit opposite effects on oral squamous cell carcinoma cell proliferation. Cancer Invest, 2011, 29 (3): 196-201.
  • 8Hollox EJ, Huffmeier U, Zeeuwen PL, et al. Psoriasis is associated with increased beta-defensin genomic copy number. Nat Genet, 2008, 40(1 ): 23-25.
  • 9Yamasaki K, Gallo RL. Antimicrobial peptides in human skin disease. Eur J Dermatol, 2008, 18(1 ): 11-21.
  • 10Liu AY, Destoumieux D, Wong AV, et al. Human beta-defensin-2 production in keratinocytes is regulated by interleukin-1, bacteria, and the state of differentiation. J Invest Dermatol, 2002, 118(2): 275-281.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部