Artificial Intelligence Driven Innovation: Advancing Mesenchymal Stem Cell Therapies and Intelligent Biomaterials for Regenerative Medicine
Huang M., Dissanayaka WL., Yiu CKY.
Narrative Review on Chronic Wound, Immune Modulation, published in Bioengineering (Basel) (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Narrative Review
- Journal
- Bioengineering (Basel) (2025)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 41463599
- PMCID
- PMC12729526
- DOI
- 10.3390/bioengineering12121302
- Citations
- 2
Abstract (original English)
Artificial intelligence (AI) is revolutionizing regenerative medicine, particularly in advancing mesenchymal stem cell (MSC) therapies and smart biomaterials. This review highlights AI's role in two core areas: First, at the biological level, AI can be used to predict MSC differentiation, immunomodulatory function, and therapeutic potential by analyzing multi-omics and imaging data, deciphering heterogeneity and improving precision. For instance, deep learning models based on MSCs' morphology can successfully predict the differentiation propensity and uncover the regulatory networks underlying the intrinsic heterogeneity. Second, in engineering, AI shifts material design from trial-and-error to data-driven approaches. Machine learning models correlate material parameters with biological properties, enabling optimized screening. Furthermore, generative AI can be used to tailor novel materials through inverse design to achieve targeted properties like accelerated wound healing. However, the current development in this field remains constrained by several severe challenges, including the fragmented nature of existing research evidence, the insufficient reproducibility of model predictions in independent cohorts, and the significant translational gap from computational predictions to in vivo validation. Future research must not only demonstrate potential but also urgently address t
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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