Song Myeongjin, Lim Kyung Min, Song Kwonwoo, Kang Geun-Ho, Kim Se Jong, Lee Youngseo, Yu Sujin, Jeong Ki-Heon, Cho Ssang-Goo
Department of Stem Cell and Regenerative Biotechnology, Molecular & Cellular Reprogramming Center and Institute of Advanced Regenerative Science, Konkuk University, Seoul, Korea.
R&D Team, StemExOne Co., Ltd., Seoul, Korea.
Int J Stem Cells. 2024 Nov 30;17(4):407-417. doi: 10.15283/ijsc24089. Epub 2024 Oct 14.
Psoriasis is a common chronic inflammatory disease in which keratinocytes proliferate abnormally due to excessive immune action. Psoriasis can be associated with various comorbidities and has a significant impact on health-related quality of life. Although many systemic treatments, including biologic agents, have been developed, topical treatment remains the main option for psoriasis management. Consequently, there is an urgent need to develop topical treatments with minimal side effects and high efficacy. Mesenchymal stem cells (MSCs) exhibit excellent immune regulation, anti-inflammatory activities, and therapeutic effects, and MSC-derived extracellular vesicles (EVs) can serve as crucial mediators of functional transfer from MSCs. Therefore, this study aimed to develop a safe and easy-to-use emulsion cream for treating psoriasis using MSC conditioned media (CM) containing EVs. We developed an enhanced Wharton's jelly MSC (WJ-MSC) culture method through a three-dimensional (3D) culture containing exogenous transforming growth factor-β3. Using the 3D culture system, we obtained CM from WJ-MSCs, which yielded a higher EV production compared to that of conventional WJ-MSC culture methods, and investigated the effect of EV-enriched 3D-WJ-MSC-CM cream on psoriasis-related inflammation. Administration of the EV-enriched 3D-WJ-MSC-CM cream significantly reduced erythema, thickness, and scaling of skin lesions, alleviated imiquimod-induced psoriasiform lesions in mice, and ameliorated histopathological changes in mouse skin. The upregulated mRNA expression of inflammatory cytokines, including IL-17a, IL-22, IL-23, and IL-36, decreased in the lesions. In conclusion, we present here a new topical treatment for psoriasis using an MSC EV-enriched cream.
银屑病是一种常见的慢性炎症性疾病,其中角质形成细胞因过度免疫作用而异常增殖。银屑病可伴有多种合并症,对健康相关生活质量有重大影响。尽管已经开发了许多全身治疗方法,包括生物制剂,但局部治疗仍然是银屑病管理的主要选择。因此,迫切需要开发副作用最小且疗效高的局部治疗方法。间充质干细胞(MSCs)具有出色的免疫调节、抗炎活性和治疗效果,而MSC衍生的细胞外囊泡(EVs)可作为MSCs功能转移的关键介质。因此,本研究旨在使用含有EVs的MSC条件培养基(CM)开发一种安全且易于使用的治疗银屑病的乳霜。我们通过含有外源性转化生长因子-β3的三维(3D)培养开发了一种增强的沃顿胶MSC(WJ-MSC)培养方法。使用3D培养系统,我们从WJ-MSCs中获得了CM,与传统的WJ-MSC培养方法相比,其产生的EV产量更高,并研究了富含EV的3D-WJ-MSC-CM乳霜对银屑病相关炎症的影响。给予富含EV的3D-WJ-MSC-CM乳霜可显著降低皮肤病变的红斑、厚度和鳞屑,减轻咪喹莫特诱导的小鼠银屑病样病变,并改善小鼠皮肤的组织病理学变化。病变中包括IL-17a、IL-22、IL-23和IL-36在内的炎性细胞因子的mRNA表达上调有所下降。总之,我们在此展示了一种使用富含MSC EV的乳霜治疗银屑病的新局部治疗方法。