Dermatology Department, Erasme Hospital, Université Libre de Bruxelles - ULB, Brussels, Belgium,
Laboratory of Stem Cells and Cancer, Unversité Libre de Bruxelles - ULB, Brussels, Belgium,
Dermatology. 2019;235(2):91-100. doi: 10.1159/000495291. Epub 2018 Dec 19.
Psoriasis is a common, chronic inflammatory skin disorder, which can significantly impact quality of life. Despite major breakthroughs in our understanding of the pathogenesis of psoriasis, the chronological order of the underlying mechanisms leading to the development of psoriatic plaques remains to be completely understood.
Although psoriasis is classically perceived as a T-cell disease, it is now well recognized that T lymphocytes do not function in exclusivity. This theory is supported by evidence from transgenic murine models that develop marked psoriasiform disease. In addition, immune cells and cytokines regulate both early and late events involved in the pathogenesis of psoriasis. Key Messages: Psoriasis is a complex disease - a dynamic interplay between immune cells, keratinocytes, and various other skin-resident cells, such as endothelial and immune cells. The contribution of each cell type is crucial in the initiation and maintenance phases of psoriatic alterations.
银屑病是一种常见的慢性炎症性皮肤病,会显著影响生活质量。尽管我们在理解银屑病发病机制方面取得了重大突破,但导致银屑病斑块发展的潜在机制的时间顺序仍未完全被理解。
尽管银屑病通常被认为是一种 T 细胞疾病,但现在人们已经认识到 T 淋巴细胞并非排他性地发挥作用。这一理论得到了转基因小鼠模型的证据支持,这些模型会发展出明显的银屑病样疾病。此外,免疫细胞和细胞因子调节银屑病发病机制中涉及的早期和晚期事件。
银屑病是一种复杂的疾病——免疫细胞、角质形成细胞和各种其他皮肤驻留细胞(如内皮细胞和免疫细胞)之间的动态相互作用。每种细胞类型在银屑病改变的启动和维持阶段都有重要贡献。