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タイトル: Regenerative therapies for lumbar degenerative disc diseases: a literature review
著者: Sono, Takashi  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-5599-0185 (unconfirmed)
Shima, Koichiro
Shimizu, Takayoshi  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-2683-0489 (unconfirmed)
Murata, Koichi  kyouindb  KAKEN_id
Matsuda, Shuichi  kyouindb  KAKEN_id
Otsuki, Bungo  kyouindb  KAKEN_id
キーワード: lumbar degenerative disc disease
regenerative therapy
cell therapy
biomaterials
growth factors
animal models
発行日: 26-Aug-2024
出版者: Frontiers Media SA
誌名: Frontiers in Bioengineering and Biotechnology
巻: 12
論文番号: 1417600
抄録: This review aimed to summarize the recent advances and challenges in the field of regenerative therapies for lumbar disc degeneration. The current first-line treatment options for symptomatic lumbar disc degeneration cannot modify the disease process or restore the normal structure, composition, and biomechanical function of the degenerated discs. Cell-based therapies tailored to facilitate intervertebral disc (IVD) regeneration have been developed to restore the IVD extracellular matrix or mitigate inflammatory conditions. Human clinical trials on Mesenchymal Stem Cells (MSCs) have reported promising outcomes exhibited by MSCs in reducing pain and improving function. Nucleus pulposus (NP) cells possess unique regenerative capacities. Biomaterials aimed at NP replacement in IVD regeneration, comprising synthetic and biological materials, aim to restore disc height and segmental stability without compromising the annulus fibrosus. Similarly, composite IVD replacements that combine various biomaterial strategies to mimic the native disc structure, including organized annulus fibrosus and NP components, have shown promise. Furthermore, preclinical studies on regenerative medicine therapies that utilize cells, biomaterials, growth factors, platelet-rich plasma (PRP), and biological agents have demonstrated their promise in repairing degenerated lumbar discs. However, these therapies are associated with significant limitations and challenges that hinder their clinical translation. Thus, further studies must be conducted to address these challenges.
著作権等: © 2024 Sono, Shima, Shimizu, Murata, Matsuda and Otsuki.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
URI: http://hdl.handle.net/2433/290613
DOI(出版社版): 10.3389/fbioe.2024.1417600
PubMed ID: 39257444
出現コレクション:学術雑誌掲載論文等

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