Evidence map›Paper›PMID 36982227›Full record

ArticleInternational journal of molecular sciences2023

A Multi-Stage Bioprocess for the Expansion of Rodent Skin-Derived Schwann Cells in Computer-Controlled Bioreactors.

Tylor Walsh, Brett Abraham, Tak-Ho Chu, Jeff Biernaskie, Rajiv Midha, Michael S Kallos

Open access · goldFull text read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

6 authors at 1 institution in 1 country.

Tylor WalshBiomedical Engineering Graduate Program, University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada.
Brett AbrahamPharmaceutical Production Research Facility, University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada.
Tak-Ho ChuHotchkiss Brain Institute, University of Calgary, 3330 Hospital Dr NW, Calgary, AB T2N 4N1, Canada.ORCID 0000-0002-3123-207X
Jeff BiernaskieHotchkiss Brain Institute, University of Calgary, 3330 Hospital Dr NW, Calgary, AB T2N 4N1, Canada.
Rajiv MidhaHotchkiss Brain Institute, University of Calgary, 3330 Hospital Dr NW, Calgary, AB T2N 4N1, Canada.
Michael S KallosPharmaceutical Production Research Facility, University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada.ORCID 0000-0002-1480-8022
University of Calgary · CA

Funding

Alberta Innovates 000Natural Sciences and Engineering Research Council RGPIN-2017-04124
6 · The paper itself

Abstract

Regenerative therapies for the treatment of peripheral nerve and spinal cord injuries can require hundreds of millions of autologous cells. Current treatments involve the harvest of Schwann cells (SCs) from nerves; however, this is an invasive procedure. Therefore, a promising alternative is using skin-derived Schwann cells (Sk-SCs), in which between 3-5 million cells can be harvested from a standard skin biopsy. However, traditional static planar culture is still inefficient at expanding cells to clinically relevant numbers. As a result, bioreactors can be used to develop reproducible bioprocesses for the large-scale expansion of therapeutic cells. Here, we present a proof-of-concept SC manufacturing bioprocess using rat Sk-SCs. With this integrated process, we were able to simulate a feasible bioprocess, taking into consideration the harvest and shipment of cells to a production facility, the generation of the final cell product, and the cryopreservation and shipment of cells back to the clinic and patient. This process started with 3 million cells and inoculated and expanded them to over 200 million cells in 6 days. Following the harvest and post-harvest cryopreservation and thaw, we were able to maintain 150 million viable cells that exhibited a characteristic Schwann cell phenotype throughout each step of the process. This process led to a 50-fold expansion, producing a clinically relevant number of cells in a 500 mL bioreactor in just 1 week, which is a dramatic improvement over current methods of expansion.

Indexed as

RodentiaSpinal Cord InjuriesAnimalsBioreactorsPeripheral NervesRatsSchwann Cellsbioprocessbioreactornerve repairscale-upSchwann cell

Identifiers

PMID36982227
PMCPMC10049355
OpenAlexW4323566376

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read90
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.