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健康状况和热失活对来源于慢性炎症性皮肤疾病供体的富生长因子血浆的蛋白质组学特征的影响。

Effect of Health Status and Heat-Induced Inactivation on the Proteomic Profile of Plasma Rich in Growth Factors Obtained from Donors with Chronic Inflammatory Skin Conditions.

机构信息

University Institute for Regenerative Medicine and Oral Implantology (UIRMI), 01007 Vitoria, Spain.

BTI-Biotechnology Institute, 01005 Vitoria, Spain.

出版信息

Biomolecules. 2024 Jun 26;14(7):763. doi: 10.3390/biom14070763.

DOI:10.3390/biom14070763
PMID:39062477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11275043/
Abstract

Atopic dermatitis, psoriasis and lichen sclerosus are among the most challenging conditions treated by dermatologists worldwide, with potentially significant physical, social and psychological impacts. Emerging evidence suggests that autologous-platelet-rich plasma could be used to manage skin inflammation. However, the presence of soluble autoimmune components could hinder their therapeutic potential. The aim of this study was to analyze the proteomic profile of plasma rich in growth factors (PRGFs) obtained from donors with inflammatory skin conditions to evaluate the impact of skin health status on the composition and bioactivity of PRGF-based treatments. Venous blood from healthy volunteers and patients with psoriasis, lichen sclerosus and atopic dermatitis was processed to produce PRGF supernatant. Half of the samples were subjected to an additional thermal treatment (56 °C) to inactivate inflammatory and immune molecules. Proteomic analysis was performed to assess the protein profile of PRGFs from healthy and non-healthy patients and the effect of Immunosafe treatment. Differential abundance patterns of several proteins related to key biological processes have been identified, including complement activation, blood coagulation, and glycolysis- and gluconeogenesis-related genes. These results also demonstrate that the thermal treatment (Immunosafe) contributes to the inactivation of the complement system and, as a consequence, reduction in the immunogenic potential of PRGF products.

摘要

特应性皮炎、银屑病和硬化性苔藓是全球皮肤科医生治疗的最具挑战性的疾病之一,它们可能会对患者的身体、社交和心理造成重大影响。新出现的证据表明,自体富血小板血浆可用于治疗皮肤炎症。然而,可溶性自身免疫成分的存在可能会阻碍其治疗潜力。本研究旨在分析从患有炎症性皮肤病的供体中获得的富含生长因子的富血小板血浆(PRGF)的蛋白质组谱,以评估皮肤健康状况对 PRGF 治疗的组成和生物活性的影响。从健康志愿者和患有银屑病、硬化性苔藓和特应性皮炎的患者中抽取静脉血以制备 PRGF 上清液。将一半样本进行额外的热处理(56°C)以灭活炎症和免疫分子。进行蛋白质组学分析以评估来自健康和非健康患者的 PRGF 的蛋白质谱以及 Immunosafe 处理的效果。已鉴定出与关键生物学过程相关的几种蛋白质的差异丰度模式,包括补体激活、血液凝固以及糖酵解和糖异生相关基因。这些结果还表明,热处理(Immunosafe)有助于补体系统的失活,并且因此降低了 PRGF 产品的免疫原性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/3eba1f28fa73/biomolecules-14-00763-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/46e67d7bf878/biomolecules-14-00763-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/07b50ee996a7/biomolecules-14-00763-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/d3411bd587da/biomolecules-14-00763-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/6e171720997e/biomolecules-14-00763-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/66c1360129e1/biomolecules-14-00763-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/b1b023587ec4/biomolecules-14-00763-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/4af7e3e578f6/biomolecules-14-00763-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/4b9bad97eb2a/biomolecules-14-00763-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/3eba1f28fa73/biomolecules-14-00763-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/46e67d7bf878/biomolecules-14-00763-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/07b50ee996a7/biomolecules-14-00763-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/d3411bd587da/biomolecules-14-00763-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/6e171720997e/biomolecules-14-00763-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/66c1360129e1/biomolecules-14-00763-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/b1b023587ec4/biomolecules-14-00763-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/4af7e3e578f6/biomolecules-14-00763-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/4b9bad97eb2a/biomolecules-14-00763-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1f/11275043/3eba1f28fa73/biomolecules-14-00763-g009.jpg

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