Harrell Carl Randall, Volarevic Ana, Arsenijevic Aleksandar, Djonov Valentin, Volarevic Vladislav
Regenerative Processing Plant, LLC, 34176 US Highway 19 N, Palm Harbor, FL 34684, USA.
Department of Psychology, Center for Research on Harmful Effects of Biological and Chemical Hazards, Faculty of Medical Sciences, University of Kragujevac, 69 Svetozara Markovica Street, 34000 Kragujevac, Serbia.
Int J Mol Sci. 2024 Dec 22;25(24):13712. doi: 10.3390/ijms252413712.
Primary Sjögren's syndrome (pSS) is an autoimmune disease characterized by the infiltration of lymphocytes on salivary and lacrimal glands, resulting in their dysfunction. Patients suffering from severe pSS have an increased risk of developing multi-organ dysfunction syndrome due to the development of systemic inflammatory response, which results in immune cell-driven injury of the lungs, kidneys, liver, and brain. Therapeutic agents that are used for the treatment of severe pSS encounter various limitations and challenges that can impact their effectiveness. Accordingly, there is a need for targeted, personalized therapy that could address the underlying detrimental immune response while minimizing side effects. Results obtained in a large number of recently published studies have demonstrated the therapeutic efficacy of mesenchymal stem cells (MSCs) in the treatment of severe pSS. MSCs, in a juxtacrine and paracrine manner, suppressed the generation of inflammatory Th1 and Th17 lymphocytes, induced the expansion of immunosuppressive cells, impaired the cross-talk between auto-reactive T and B cells, and prevented the synthesis and secretion of auto-antibodies. Additionally, MSC-derived growth and trophic factors promoted survival and prevented apoptosis of injured cells in inflamed lacrimal and salivary glands, thereby enhancing their repair and regeneration. In this review article, we summarized current knowledge about the molecular mechanisms that are responsible for the beneficial effects of MSCs in the suppression of immune cell-driven injury of exocrine glands and vital organs, paving the way for a better understanding of their therapeutic potential in the targeted therapy of severe pSS.
原发性干燥综合征(pSS)是一种自身免疫性疾病,其特征是淋巴细胞浸润唾液腺和泪腺,导致其功能障碍。患有严重pSS的患者由于全身炎症反应的发展而发生多器官功能障碍综合征的风险增加,这会导致免疫细胞驱动的肺、肾、肝和脑损伤。用于治疗严重pSS的治疗药物面临各种限制和挑战,可能会影响其疗效。因此,需要有针对性的个性化治疗,既能解决潜在的有害免疫反应,又能将副作用降至最低。最近发表的大量研究结果表明,间充质干细胞(MSCs)在治疗严重pSS方面具有治疗效果。MSCs以旁分泌和自分泌的方式,抑制炎性Th1和Th17淋巴细胞的生成,诱导免疫抑制细胞的扩增,破坏自身反应性T细胞和B细胞之间的相互作用,并阻止自身抗体的合成和分泌。此外,MSCs衍生的生长和营养因子可促进炎症泪腺和唾液腺中受损细胞的存活并防止其凋亡,从而增强其修复和再生能力。在这篇综述文章中,我们总结了目前关于MSCs在抑制免疫细胞驱动的外分泌腺和重要器官损伤中发挥有益作用的分子机制的知识,为更好地理解其在严重pSS靶向治疗中的治疗潜力铺平了道路。