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活体生物药物以及组织来源如何影响用于治疗心力衰竭的间充质干细胞疗法。

Living biodrugs and how tissue source influences mesenchymal stem cell therapeutics for heart failure.

作者信息

Shah Siddharth, Nawaz Huzaifa Sabir, Qazi Muhammad Saeed, Jain Hritvik, Lucke-Wold Brandon

机构信息

Lillian S Wells Department of Neurosurgery, University of Florida, Gainesville, FL 32608, United States.

Department of Internal Medicine, Services Institute of Medical Sciences, Lahore 54000, Pakistan.

出版信息

World J Cardiol. 2024 Nov 26;16(11):619-625. doi: 10.4330/wjc.v16.i11.619.

Abstract

In this editorial we comment on the article by Safwan M . We especially focused on the cardiac function restoration by the use of mesenchymal stem cells (MSCs) therapy for heart failure (HF), which has emerged as a new treatment approach as "Living Biodrugs". HF remains a significant clinical challenge due to the heart's inability to pump blood effectively, despite advancements in medical and device-based therapies. MSCs have emerged as a promising therapeutic approach, offering benefits beyond traditional treatments through their ability to modulate inflammation, reduce fibrosis, and promote endogenous tissue regeneration. MSCs can be derived from various tissues, including bone marrow and umbilical cord. Umbilical cord-derived MSCs exhibit superior expansion capabilities, making them an attractive option for HF therapy. Conversely, bone marrow-derived MSCs have been extensively studied for their potential to improve cardiac function but face challenges related to cell retention and delivery. Future research is focusing on optimizing MSC sources, enhancing differentiation and immune modulation, and improving delivery methods to overcome current limitations.

摘要

在这篇社论中,我们对萨夫万·M的文章进行评论。我们特别关注了通过使用间充质干细胞(MSC)疗法治疗心力衰竭(HF)来恢复心脏功能,这已作为一种“活生物药物”成为一种新的治疗方法。尽管医学和基于器械的治疗取得了进展,但由于心脏无法有效泵血,HF仍然是一个重大的临床挑战。MSC已成为一种有前景的治疗方法,通过其调节炎症、减少纤维化和促进内源性组织再生的能力,提供了超越传统治疗的益处。MSC可以从包括骨髓和脐带在内的各种组织中获得。脐带来源的MSC具有卓越的扩增能力,使其成为HF治疗的一个有吸引力的选择。相反,骨髓来源的MSC因其改善心脏功能的潜力而受到广泛研究,但面临与细胞保留和递送相关的挑战。未来的研究集中在优化MSC来源、增强分化和免疫调节以及改进递送方法以克服当前的局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7c9/11586726/6bedd71ef578/WJC-16-619-g001.jpg

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