唾液腺的药物和干细胞递送-简要回顾。

IF 5.4
Janaki Iyer, Arvind Hariharan, Riho Kanai, Yuanyuan Peng, Mohammed Badwelan, Yoshinori Sumita, Simon D Tran
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引用次数: 0

摘要

系统平衡、口腔健康和消化取决于唾液腺(SGs)的健康。SG疾病,如Sjögren综合征、口腔颌面癌和放射性损伤,通常与口干症相关,严重影响患者的生活质量。目前的治疗方式主要提供对症治疗,而没有解决基本的潜在组织损伤或促进再生。新兴的药物和干细胞治疗可能恢复SG功能,但量身定制的递送、有效性和安全性问题限制了它们的临床应用。涵盖领域:本综述总结了系统和局部干细胞和药物管理的临床前和临床研究结果。我们讨论了各种SG情况,以使治疗方法与疾病的特定需求相匹配,并强调了准确,高效的给药系统的必要性,以改善结果并减少不良反应。我们总结了现有的局限性,未来的观点和前瞻性的SG医学再生治疗进展。专家意见:SGs药物和干细胞输送系统的进步提供了超越症状缓解的潜力,而是使受损组织再生。尽管免疫排斥、安全性和成本等挑战仍然很大,但这些方法有望提供更有针对性、更具成本效益和更持久的治疗。未来的研究应侧重于改善干细胞的来源、传递和跟踪,同时结合基因编辑、纳米载体和组织工程等技术来提高疗效。最终,治疗策略转向再生解决方案,旨在恢复SG功能,减少系统副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug and stem cells delivery to salivary glands - a concise review.

Introduction: Systemic equilibrium, oral health, and digestion depend on the health of the salivary glands (SGs). SG disorders, such as Sjögren's syndrome, oral and maxillofacial cancer, and radiation-induced damage, are usually associated with xerostomia, which severely impacts the patient's quality of life. Current therapeutic modalities primarily provide symptomatic therapy without addressing the basic underlying tissue damage or promoting regeneration. Emerging pharmacological and stem cell treatments may restore SG function, but tailored delivery, effectiveness, and safety issues restrict their clinical application.

Areas covered: This review summarizes preclinical and clinical findings on systemic and localized stem cell and pharmaceutical drug administration. We discuss various SG conditions to match therapy methods to disease-specific demands and underline the necessity for accurate, efficient delivery systems to improve results and reduce adverse effects. We conclude with existing limits, future views, and prospective SG medicine regenerative therapy advancements.

Expert opinion: Advancements in drug and stem cell delivery systems for SGs offer the potential to move beyond symptomatic relief and instead regenerate damaged tissues. These approaches promise more targeted, cost-effective, and long-lasting therapies, though challenges like immune rejection, safety, and cost remain significant. Future research should focus on improving stem cell sources, delivery, and tracking, while integrating technologies such as gene editing, nanocarriers, and tissue engineering to enhance efficacy. Ultimately, treatment strategies are shifting toward regenerative solutions aimed at restoring SG function with fewer systemic side effects.

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