Department of Dermatology and Allergology, University of Szeged, Szeged, Hungary.
HCEMM-SZTE Skin Research Group, Szeged, Hungary.
Exp Dermatol. 2021 Jun;30(6):765-772. doi: 10.1111/exd.14267. Epub 2021 Jan 16.
Current data suggest that tissue microenvironment control immune functions. Therefore, understanding the tissue environment in which immune activation occurs will enhance our capability to interfere with abnormal immune pathology. Here, we argue that studying the constitutively abnormal functions of clinically uninvolved psoriatic skin in patients with plaque type psoriasis is very important to better understand psoriasis pathobiology, because non-lesional skin provides the tissue environment in which the psoriatic lesion develops. A key question in psoriasis is what initiates the abnormal, uncontrolled immune activation in the first place and the answer may lie in the skin. In light of this concept, we summarize abnormalities at the dermal-epidermal junction region which shows a special "non-healing-like" micro-wound phenotype in the psoriatic non-lesional skin that may act as a crucial susceptibility factor in the development of the disease.
目前的数据表明,组织微环境控制着免疫功能。因此,了解免疫激活发生的组织环境将提高我们干预异常免疫病理的能力。在这里,我们认为研究斑块型银屑病患者中无临床受累的银屑病皮肤的固有异常功能对于更好地理解银屑病发病机制非常重要,因为非皮损皮肤提供了银屑病皮损发展的组织环境。银屑病的一个关键问题是最初是什么引发了异常的、不受控制的免疫激活,答案可能在于皮肤。鉴于这一概念,我们总结了在银屑病非皮损皮肤中,表皮-真皮交界处区域的异常表现,其表现出一种特殊的“非愈合样”微创伤表型,这可能是疾病发展的一个关键易感因素。