Evidence map›Paper›PMID 39353832›Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2024

Bioreactor-produced iPSCs-derived dopaminergic neuron-containing neural microtissues innervate and normalize rotational bias in a dose-dependent manner in a Parkinson rat model.

Nicolas Prudon, Lucía Cordero-Espinoza, Myriam Abarkan, Basile Gurchenkov, Chloé Morel, Marilyn Lepleux, Valérie De Luca, Maxime Lartigue, Hélène Cabanas, Nadège Pujol and 25 more

Abstract read
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

35 authors.

Nicolas PrudonUniversité de Bordeaux, CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France; TreeFrog Therapeutics, Bât A, F-33600 Pessac, France. Electronic address: nicolas.prudon@u-bordeaux.fr.
Lucía Cordero-EspinozaTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Myriam AbarkanTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Basile GurchenkovTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Chloé MorelTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Marilyn LepleuxTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Valérie De LucaTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Maxime LartigueTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Hélène CabanasTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Nadège PujolTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Loanne MilvoyTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Pauline MorandTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Fabien MoncaubeigTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Hélène WurtzTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Léa PoinçotTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Maëlle De MarcoTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Agathe JonckeauTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Justine PletenkaTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Elisa LuquetTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Andrea SoveraTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Jérôme HardoüinTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Inês Januario NevesTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Anaïs Machado-HitauTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Kathleen SchmitTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Lucie PiouceauTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Solenn GuilbertTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Lucie Manache-AlbericiTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Michaël Lanero FidalgoTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Guillaume DabéeUniversité de Bordeaux, CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France; PIV-EXPE, Centre Broca, Université de Bordeaux, F-33000 Bordeaux, France.
Thibault DufourdTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Jens SchroederTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Kévin AlessandriTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Erwan BezardUniversité de Bordeaux, CNRS, Institut des Maladies Neurodégénératives, UMR 5293, F-33000 Bordeaux, France.
Emilie FaggianiTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.
Maxime FeyeuxTreeFrog Therapeutics, Bât A, F-33600 Pessac, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A breadth of preclinical studies now support the rationale of pluripotent stem cell-derived cell replacement therapies to alleviate motor symptoms in Parkinsonian patients. Replacement of the primary dysfunctional cell population in the disease, i.e. the A9 dopaminergic neurons, is the major focus of these therapies. To achieve this, most therapeutical approaches involve grafting single-cell suspensions of DA progenitors. However, most cells die during the transplantation process, as cells face anoïkis. One potential solution to address this challenge is to graft solid preparations, i.e. adopting a 3D format. Cryopreserving such a format remains a major hurdle and is not exempt from causing delays in the time to effect, as observed with cryopreserved single-cell DA progenitors. Here, we used a high-throughput cell-encapsulation technology coupled with bioreactors to provide a 3D culture environment enabling the directed differentiation of hiPSCs into neural microtissues. The proper patterning of these neural microtissues into a midbrain identity was confirmed using orthogonal methods, including qPCR, RNAseq, flow cytometry and immunofluorescent microscopy. The efficacy of the neural microtissues was demonstrated in a dose-dependent manner using a Parkinsonian rat model. The survival of the cells was confirmed by post-mortem histological analysis, characterised by the presence of human dopaminergic neurons projecting into the host striatum. The work reported here is the first bioproduction of a cell therapy for Parkinson's disease in a scalable bioreactor, leading to a full behavioural recovery 16 weeks after transplantation using cryopreserved 3D format.

Indexed as

BioreactorsDopaminergic NeuronsInduced Pluripotent Stem CellsAnimalsCell DifferentiationDisease Models, AnimalHumansMaleParkinson DiseaseRatsRats, Sprague-Dawley3D cell formatCell therapyMidbrainOff-the-shelfOrganoidRegenerative medicine

Identifiers

PMID39353832
PMCPMC11581877

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.