Suppr超能文献

真皮 CD11c+树突状细胞的增加与银屑病皮损的早期发展有关。

Rise in dermal CD11c+ dendritic cells associates with early-stage development of psoriatic lesions.

机构信息

Department of Dermatology, Academic Medical Center, University of Amsterdam, The Netherlands.

出版信息

Arch Dermatol Res. 2012 Aug;304(6):443-9. doi: 10.1007/s00403-012-1231-7. Epub 2012 Mar 22.

Abstract

There is limited information available regarding the phenotype and function of leukocytes involved in the earliest stages of psoriatic lesion development. In this study, we examined the presence of different types of leukocytes in psoriatic point lesions collected at three 1-week interval time points from a recent and simultaneously formed group of point lesions. The cells were quantified and compared with K16 expression and epidermal thickness, both typically increased in this disease and considered as hallmarks. We found a significant correlation between K16(+) cell increment and the increase in epidermal thickness in the timeframe of 14 days. The change in CD3(+), CD4(+), and CD8(+) T-cell numbers in the dermis showed a significant association with these two features from d7 to d14, whereas in the epidermis only CD8(+) T cells demonstrated a significant correlation. Remarkably, the relationship between T cells and disease progression was preceded by a significant correlation of CD11c(+) dendritic cells (DCs) with K16 expression and epidermal thickness from baseline onwards. Interestingly, there was also a numeric correlation of CD11c(+) DCs with the CD3(+) T-cell shifts from d7 to d14. A significant correlation was also found between dermal CD14(+) cells and K16 expression from d7 to d14. BDCA-2(+) plasmacytoid DCs were absent in non-lesional skin, but found at low numbers in most lesions. The change in plasmacytoid DC or neutrophil numbers did not correlate with lesion development. In conclusion, our study suggests a relevant role for T cells, and in particular dermal CD11c(+) DCs, in the earliest stage of psoriatic lesion development.

摘要

关于参与银屑病皮损早期发展的白细胞表型和功能,目前相关信息有限。在本研究中,我们检查了最近同时形成的一组点病变中,在三个 1 周间隔时间点采集的银屑病点病变中不同类型白细胞的存在情况。对这些细胞进行了定量,并与 K16 表达和表皮厚度进行了比较,这两种特征在该疾病中通常增加,被认为是标志。我们发现,在 14 天的时间内,K16(+)细胞增加与表皮厚度增加之间存在显著相关性。真皮中 CD3(+)、CD4(+)和 CD8(+)T 细胞数量的变化与 d7 至 d14 这两个特征呈显著相关性,而在表皮中仅 CD8(+)T 细胞显示出显著相关性。值得注意的是,T 细胞与疾病进展之间的关系先于 CD11c(+)树突状细胞 (DC) 与 K16 表达和基线时的表皮厚度之间的显著相关性。有趣的是,从 d7 到 d14,CD11c(+)DCs 与 CD3(+)T 细胞数量的变化之间也存在数值相关性。真皮中 CD14(+)细胞与 d7 至 d14 之间的 K16 表达也存在显著相关性。非皮损皮肤中缺乏 BDCA-2(+)浆细胞样 DC,但在大多数皮损中可发现少量浆细胞样 DC。浆细胞样 DC 或中性粒细胞数量的变化与病变发展无关。总之,我们的研究表明 T 细胞,特别是真皮 CD11c(+)DC,在银屑病皮损早期发展中具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ec7/3401310/b5d4bb1c5106/403_2012_1231_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验