FOXP3型
免疫学
免疫系统
人体皮肤
免疫组织化学
真皮
生物
CD8型
转录因子
利基
细胞生物学
病理
医学
解剖
遗传学
基因
生态学
作者
Courtney E. Macon,Annie Yang,Dhara Patel,Jeffrey P. North,Michael D. Rosenblum,Jarish N. Cohen
摘要
ABSTRACT Regulatory T cells (Tregs) are specialised T lymphocytes that sit at the nexus of immune regulation and tissue repair. While it is appreciated that a substantial number of Tregs are present in healthy human skin, less is known about their microanatomic spatial localisation. Knowledge about the specialised niches that Tregs occupy may aid in rational drug development to treat dermatologic diseases. Thus, we performed multiplexed immunohistochemistry for CD4 and FOXP3 (the lineage‐defining transcription factor of Tregs) on healthy skin sections obtained from eight different cutaneous sites, and quantified Tregs and Tcon in distinct regions. We found that Tregs (CD4 + FOXP3 + ) comprised roughly 20% of CD4 + T cells in skin and that Tregs and T‐conventional cells (Tcon; CD4 + Foxp3 − ) are enriched in follicularly dense skin and show preferential accumulation in perivascular and perifollicular niches in the upper dermis. Additionally, male skin shows a significant increase in the numbers of Tregs and Tcon, while female skin shows a higher Tcon:Treg ratio. We also find that the frequency of skin Tregs declines over time. Overall, we conclude that the upper dermal perivascular region is a niche that supports the accumulation of CD4 + T cells in steady‐state human skin.
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