Evidence map›Paper›PMID 37802038›Full record

ArticleCell stem cell2023

Human pallial MGE-type GABAergic interneuron cell therapy for chronic focal epilepsy.

Marina Bershteyn, Sonja Bröer, Mansi Parekh, Yves Maury, Steven Havlicek, Sonja Kriks, Luis Fuentealba, Seonok Lee, Robin Zhou, Geetha Subramanyam and 20 more

Registry-linked trialAbstract read
In one paragraph

Article in Cell stem cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05135091 (A Study of Inhibitory Interneurons), which is not on this map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
–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.

NCT05135091 phase3recruitingnot on this map

A Study of Inhibitory Interneurons (NRTX-1001) in Drug-Resistant Unilateral Mesial Temporal Lobe Epilepsy (MTLE)

TypeinterventionalSponsorNeurona TherapeuticsRan2022 to 2043Enrolled88ConditionsMesial Temporal Lobe EpilepsyArmsNRTX-1001, Sham Comparator
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

30 authors.

Marina BershteynNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Sonja BröerNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Mansi ParekhNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Yves MauryNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Steven HavlicekNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Sonja KriksNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Luis FuentealbaNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Seonok LeeNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Robin ZhouNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Geetha SubramanyamNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Meliz SezanNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Eric Steven SevillaNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Whitney BlankenbergerNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Julien SpatazzaNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Li ZhouDepartment of Neurology, University of California, San Francisco, San Francisco, CA 94143, USA; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA 94143, USA.
Hubert NethercottNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
David TraverNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Philip HampelNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Hannah KimNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Michael WatsonNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Naomi SalterNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Anastasia NesterovaNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Wai AuNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Arnold KriegsteinDepartment of Neurology, University of California, San Francisco, San Francisco, CA 94143, USA; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA 94143, USA.
Arturo Alvarez-BuyllaThe Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA 94143, USA; Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.
John RubensteinDepartment of Psychiatry, Weill Institute for Neurosciences, Kavli Institute for Fundamental Neuroscience, University of California, San Francisco, San Francisco, CA 94143, USA.
Gautam BanikNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Alessandro BulfoneNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Catherine PriestNeurona Therapeutics Inc., South San Francisco, CA 94080, USA.
Cory R NicholasNeurona Therapeutics Inc., South San Francisco, CA 94080, USA. Electronic address: cory@neuronatx.com.

Funding

Genetic Control of Basal Telencephalic DevelopmentR01MH081880 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RUBENSTEIN, JOHN L. R. · 2009 to 2023
$8.1M
NIMH NIH HHS R01 MH081880
6 · The paper itself

Abstract

Mesial temporal lobe epilepsy (MTLE) is the most common focal epilepsy. One-third of patients have drug-refractory seizures and are left with suboptimal therapeutic options such as brain tissue-destructive surgery. Here, we report the development and characterization of a cell therapy alternative for drug-resistant MTLE, which is derived from a human embryonic stem cell line and comprises cryopreserved, post-mitotic, medial ganglionic eminence (MGE) pallial-type GABAergic interneurons. Single-dose intrahippocampal delivery of the interneurons in a mouse model of chronic MTLE resulted in consistent mesiotemporal seizure suppression, with most animals becoming seizure-free and surviving longer. The grafted interneurons dispersed locally, functionally integrated, persisted long term, and significantly reduced dentate granule cell dispersion, a pathological hallmark of MTLE. These disease-modifying effects were dose-dependent, with a broad therapeutic range. No adverse effects were observed. These findings support an ongoing phase 1/2 clinical trial (NCT05135091) for drug-resistant MTLE.

Indexed as

Epilepsy, Temporal LobeHippocampusAnimalsBrainHumansInterneuronsMiceSeizurescell therapyepilepsyGABAhESCinterneuronMGEseizureTLEtransplant

Identifiers

PMID37802038
PMCPMC10993865

What OpenQuestion holds

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Registered trials

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.