Evidence map›Paper›PMID 31877913›Full record

ArticleInternational journal of molecular sciences2019

Long-Term Stability and Differentiation Potential of Cryopreserved cGMP-Compliant Human Induced Pluripotent Stem Cells.

Mehdi Shafa, Tylor Walsh, Krishna Morgan Panchalingam, Thomas Richardson, Laura Menendez, Xinghui Tian, Sahana Suresh Babu, Saedeh Dadgar, Justin Beller, Fan Yang and 1 more

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Commercialization of Cell Therapies: A CDMO Perspective.Advances in experimental medicine and biology · 2025
    Review
  4. Article
  5. Review
  6. Review
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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

11 authors at 1 institution in 1 country.

Mehdi ShafaCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.ORCID 0000-0003-3560-2717
Tylor WalshCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Krishna Morgan PanchalingamCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Thomas RichardsonCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Laura MenendezCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Xinghui TianCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Sahana Suresh BabuCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.ORCID 0000-0002-4200-6799
Saedeh DadgarCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Justin BellerCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Fan YangCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Behnam Ahmadian BaghbaderaniCell Therapy Process Department, Lonza Houston, Inc., Houston, TX 77047, USA.
Lonza (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical effectiveness of human induced pluripotent stem cells (iPSCs) is highly dependent on a few key quality characteristics including the generation of high quality cell bank, long-term genomic stability, post-thaw viability, plating efficiency, retention of pluripotency, directed differentiation, purity, potency, and sterility. We have already reported the establishment of iPSC master cell banks (MCBs) and working cell banks (WCBs) under current good manufacturing procedure (cGMP)-compliant conditions. In this study, we assessed the cellular and genomic stability of the iPSC lines generated and cryopreserved five years ago under cGMP-compliant conditions. iPSC lines were thawed, characterized, and directly differentiated into cells from three germ layers including cardiomyocytes (CMs), neural stem cells (NSCs), and definitive endoderm (DE). The cells were also expanded in 2D and 3D spinner flasks to evaluate their long-term expansion potential in matrix-dependent and feeder-free culture environment. All three lines successfully thawed and attached to the L7

Indexed as

CryopreservationCell DifferentiationCell LineHumansInduced Pluripotent Stem CellsMyocytes, CardiacNeural Stem CellsTime FactorscGMPcryopreservationdifferentiationinduced pluripotent stem cellsstabilityTelomere

Identifiers

PMID31877913
PMCPMC6982271
OpenAlexW2996431718

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.