ArticleStem cell research & therapy2025
Clinical-grade allogeneic amniotic fluid stem cell banking: quality control for therapeutic applications and drug development.
Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAllogeneic mesenchymal stem cells (MSCs) offer significant advantages for various medical treatments. However, maintaining an allogeneic MSC bank presents challenges due to concerns about heterogeneity, which directly affects their efficacy. Additionally, issues related to cell senescence can arise even after a short period of serial passaging. Amniotic fluid mesenchymal stem cells (AF-MSCs) demonstrate greater proliferation efficiency compared to other MSCs. They can form clonal cell lines that generate a homogeneous population and can expand in long-term cultures without undergoing cellular senescence. Therefore, this study introduces a method for establishing cell lines and a banking system for AF-MSCs, providing high-quality, authentic human MSCs for clinical applications.
methodsIn this research, we isolated clonal AF-MSCs to select them for the creation of AF-MSC stock through long-term serial passaging. We developed a three-tier cell banking system, which includes an AF-MSC stock, a Master Cell Bank at passage 4, and a Working Cell Bank at passage 9. Standard characteristics were employed to verify identity, safety, and quality control assessments.
resultsThree out of twelve AF-MSC clones were selected to exemplify cell line establishment, the creation of a three-tier banking system, and quality control evaluations to determine their suitability for clinical-grade cell lines in medical applications.
conclusionsThis study offers a comprehensive technical and translational overview of establishing an allogeneic amniotic fluid mesenchymal stem cell bank, tailored for medical applications and drug development.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.