Evidence map›Paper›PMID 31877727›Full record

ArticleInternational journal of molecular sciences2019

End-to-End Platform for Human Pluripotent Stem Cell Manufacturing.

Puspa R Pandey, Amarel Tomney, Marites T Woon, Nicholas Uth, Farjad Shafighi, Igor Ngabo, Haritha Vallabhaneni, Yonatan Levinson, Eytan Abraham, Inbar Friedrich Ben-Nun

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 40 citations in OpenAlex.

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  15. Advances in Manufacturing Cardiomyocytes from Human Pluripotent Stem Cells.Annual review of chemical and biomolecular engineering · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Puspa R PandeyCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Amarel TomneyCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Marites T WoonCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Nicholas UthCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Farjad ShafighiCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Igor NgaboCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Haritha VallabhaneniCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Yonatan LevinsonCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Eytan AbrahamCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Inbar Friedrich Ben-NunCell and Gene Therapy Research and Development, Lonza Inc., Rockville, MD 20850, USA.
Lonza (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Industrialization of stem-cell based therapies requires innovative solutions to close the gap between research and commercialization. Scalable cell production platforms are needed to reliably deliver the cell quantities needed during the various stages of development and commercial supply. Human pluripotent stem cells (hPSCs) are a key source material for generating therapeutic cell types. We have developed a closed, automated and scalable stirred tank bioreactor platform, capable of sustaining high fold expansion of hPSCs. Such a platform could facilitate the in-process monitoring and integration of online monitoring systems, leading to significantly reduced labor requirements and contamination risk. hPSCs are expanded in a controlled bioreactor using perfused xeno-free media. Cell harvest and concentration are performed in closed steps. The hPSCs can be cryopreserved to generate a bank of cells, or further processed as needed. Cryopreserved cells can be thawed into a two-dimensional (2D) tissue culture platform or a three-dimensional (3D) bioreactor to initiate a new expansion phase, or be differentiated to the clinically relevant cell type. The expanded hPSCs express hPSC-specific markers, have a normal karyotype and the ability to differentiate to the cells of the three germ layers. This end-to-end platform allows a large scale expansion of high quality hPSCs that can support the required cell demand for various clinical indications.

Indexed as

Automation, LaboratoryBioreactorsCell DifferentiationCell ProliferationCells, CulturedCellular Reprogramming TechniquesHumansInduced Pluripotent Stem CellsMyocytes, CardiacPrimary Cell Cultureallogeneic cell therapyautomationbioreactorsdifferentiationexpansionhuman pluripotent stem cellskSepmicrocarriers

Identifiers

PMID31877727
PMCPMC6981419
OpenAlexW2995477520

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.