Evidence map›Paper›PMID 24726657›Full record

ArticleCytotherapy2014

Efficient manufacturing of therapeutic mesenchymal stromal cells with the use of the Quantum Cell Expansion System.

Patrick J Hanley, Zhuyong Mei, April G Durett, Maria da Graca Cabreira-Hansen, Marie da Graca Cabreira-Harrison, Mariola Klis, Wei Li, Yali Zhao, Bing Yang, Kaushik Parsha and 7 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cytotherapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

67 citing papers in PubMed, 153 citations in OpenAlex.

  1. Allogeneic Bone Marrow-Derived Mesenchymal Stem Cells for Parkinson's Disease: A Randomized Trial.Movement disorders : official journal of the Movement Disorder Society · 2025
    Trial
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  7. Stem Cell Therapy in Ischemic Heart Failure.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2025
    Review
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7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
    Erratum.2014 · Cabreira-Harrison, Marie da Graca [corrected to Cabreira-Hansen, Maria da Graca]
5 · Who and what money

Authors and funding

17 authors at 7 institutions in 1 country.

Patrick J HanleyCenter for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA; Program for Cell Enhancement and Technologies for Immunotherapy, Sheikh Zayed Institute for Pediatric Surgical Innovation, and The Center for Cancer and Immunology Research, Children's National Medical Center, Washington, DC, USA. Electronic address: phanley@childrensnational.org.
Zhuyong MeiCenter for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA.
April G DurettCenter for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA.
Maria da Graca Cabreira-Hansen
Marie da Graca Cabreira-HarrisonThe Texas Heart Institute, St Luke's Episcopal Hospital, Houston, Texas, USA.
Mariola KlisCenter for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA.
Wei LiCenter for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA.
Yali ZhaoCenter for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA.
Bing YangDepartment of Neurology, University of Texas Health Science Center, Houston, Texas, USA.
Kaushik ParshaDepartment of Neurology, University of Texas Health Science Center, Houston, Texas, USA.
Osman MirDepartment of Neurology, University of Texas Health Science Center, Houston, Texas, USA.
Farhaan VahidyDepartment of Neurology, University of Texas Health Science Center, Houston, Texas, USA.
Debra BloomUniversity of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, USA.
R Brent RiceTerumo BCT, Lakewood, Colorado, USA.
Peiman HemattiUniversity of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, USA.
Sean I SavitzDepartment of Neurology, University of Texas Health Science Center, Houston, Texas, USA.
Adrian P GeeCenter for Cell and Gene Therapy, Texas Children's Hospital, The Methodist Hospital, and Baylor College of Medicine, Houston, Texas, USA.
The University of Texas Health Science Center at Houston · USTexas Children's Hospital · USBaylor College of Medicine · USUniversity of Wisconsin–Madison · USMethodist Hospital · USSt. Luke's Episcopal Hospital · USTerumo (United States) · US

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
NCI NIH HHS P30 CA125123NHLBI NIH HHS HHSN268201000007C
6 · The paper itself

Abstract

backgroundThe use of bone marrow-derived mesenchymal stromal cells (MSCs) as a cellular therapy for various diseases, such as graft-versus-host disease, diabetes, ischemic cardiomyopathy and Crohn's disease, has produced promising results in early-phase clinical trials. However, for widespread application and use in later phase studies, manufacture of these cells must be cost-effective, safe and reproducible. Current methods of manufacturing in flasks or cell factories are labor-intensive, involve a large number of open procedures and require prolonged culture times.

methodsWe evaluated the Quantum Cell Expansion System for the expansion of large numbers of MSCs from unprocessed bone marrow in a functionally closed system and compared the results with a flask-based method currently in clinical trials.

resultsAfter only two passages, we were able to expand a mean of 6.6 × 10(8) MSCs from 25 mL of bone marrow reproducibly. The mean expansion time was 21 days, and cells obtained were able to differentiate into all three lineages: chondrocytes, osteoblasts and adipocytes. The Quantum was able to generate the target cell number of 2.0 × 10(8) cells in an average of 9 fewer days and in half the number of passages required during flask-based expansion. We estimated that the Quantum would involve 133 open procedures versus 54,400 in flasks when manufacturing for a clinical trial. Quantum-expanded MSCs infused into an ischemic stroke rat model were therapeutically active.

conclusionsThe Quantum is a novel method of generating high numbers of MSCs in less time and at lower passages when compared with flasks. In the Quantum, the risk of contamination is substantially reduced because of the substantial decrease in open procedures.

Indexed as

Cell- and Tissue-Based TherapyCell Culture TechniquesAnimalsBioreactorsBone Marrow CellsCell DifferentiationCell LineageHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationRatscell culture expansiongood manufacturing practicesmesenchymal stromal cellsQuantumstroke

Identifiers

PMID24726657
PMCPMC4087082
OpenAlexW2146216718

What OpenQuestion holds

Textmetadata
LicenceTDM
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.