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炎症改变了人皮肤来源前体细胞的分泌组和免疫调节特性。

Inflammation Alters the Secretome and Immunomodulatory Properties of Human Skin-Derived Precursor Cells.

机构信息

Department of In Vitro Toxicology and Dermato-Cosmetology, Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel, 1090 Brussels, Belgium.

Department of Clinical Chemistry, Microbiology and Immunology, Faculty of Medicine and Health Sciences, Universiteit Gent, 9000 Ghent, Belgium.

出版信息

Cells. 2020 Apr 8;9(4):914. doi: 10.3390/cells9040914.

DOI:10.3390/cells9040914
PMID:32276503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7226778/
Abstract

Human skin-derived precursors (SKP) represent a group of somatic stem/precursor cells that reside in dermal skin throughout life that harbor clinical potential. SKP have a high self-renewal capacity, the ability to differentiate into multiple cell types and low immunogenicity, rendering them key candidates for allogeneic cell-based, off-the-shelf therapy. However, potential clinical application of allogeneic SKP requires that these cells retain their therapeutic properties under all circumstances and, in particular, in the presence of an inflammation state. Therefore, in this study, we investigated the impact of pro-inflammatory stimulation on the secretome and immunosuppressive properties of SKP. We demonstrated that pro-inflammatory stimulation of SKP significantly changes their expression and the secretion profile of chemo/cytokines and growth factors. Most importantly, we observed that pro-inflammatory stimulated SKP were still able to suppress the graft-versus-host response when cotransplanted with human PBMC in severe-combined immune deficient (SCID) mice, albeit to a much lesser extent than unstimulated SKP. Altogether, this study demonstrates that an inflammatory microenvironment has a significant impact on the immunological properties of SKP. These alterations need to be taken into account when developing allogeneic SKP-based therapies.

摘要

人皮肤源性前体细胞(SKP)是一群位于皮肤真皮层中的体干细胞/前体细胞,它们终生存在并具有临床潜力。SKP 具有高自我更新能力、能够分化为多种细胞类型以及低免疫原性,使其成为同种异体基于细胞的现成治疗的关键候选物。然而,同种异体 SKP 的潜在临床应用要求这些细胞在所有情况下都保持其治疗特性,特别是在炎症状态下。因此,在这项研究中,我们研究了促炎刺激对 SKP 分泌组和免疫抑制特性的影响。我们表明,SKP 的促炎刺激会显著改变其化学/细胞因子和生长因子的表达和分泌谱。最重要的是,我们观察到,当与人类 PBMC 在严重联合免疫缺陷(SCID)小鼠中共移植时,促炎刺激的 SKP 仍然能够抑制移植物抗宿主反应,尽管其抑制作用比未刺激的 SKP 小得多。总的来说,这项研究表明,炎症微环境对 SKP 的免疫学特性有重大影响。在开发基于同种异体 SKP 的治疗方法时,需要考虑这些变化。

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