Evidence map›Paper›PMID 35645733›Full record

ReviewFrontiers in molecular neuroscience2022

Gene and Cell Therapy for Epilepsy: A Mini Review.

Alisa A Shaimardanova, Daria S Chulpanova, Aysilu I Mullagulova, Zaid Afawi, Rimma G Gamirova, Valeriya V Solovyeva, Albert A Rizvanov

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Epilepsy grand challenge 2025.Frontiers in neurology · 2025
    Article
  7. Adeno-Associated Viral Vectors in the Treatment of Epilepsy.International journal of molecular sciences · 2024
    Review
  8. Review
  9. New epilepsy therapies in development.Nature reviews. Drug discovery · 2024
    Review
  10. Review
  11. Review
  12. Is there room in epilepsy for the claustrum?Frontiers in systems biology · 2024
    Article
  13. Article
  14. Review
  15. Article
  16. Gene Therapy of Sphingolipid Metabolic Disorders.International journal of molecular sciences · 2023
    Review
  17. Review
  18. 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

7 authors at 2 institutions in 2 countries.

Alisa A ShaimardanovaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Daria S ChulpanovaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Aysilu I MullagulovaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Zaid AfawiCenter for Neuroscience, Ben Gurion University of the Negev, Be'er Sheva, Israel.
Rimma G GamirovaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Valeriya V SolovyevaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Albert A RizvanovInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Kazan Federal University · RUBen-Gurion University of the Negev · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy is a chronic non-infectious disease of the brain, characterized primarily by recurrent unprovoked seizures, defined as an episode of disturbance of motor, sensory, autonomic, or mental functions resulting from excessive neuronal discharge. Despite the advances in the treatment achieved with the use of antiepileptic drugs and other non-pharmacological therapies, about 30% of patients suffer from uncontrolled seizures. This review summarizes the currently available methods of gene and cell therapy for epilepsy and discusses the development of these approaches. Currently, gene therapy for epilepsy is predominantly adeno-associated virus (AAV)-mediated delivery of genes encoding neuro-modulatory peptides, neurotrophic factors, enzymes, and potassium channels. Cell therapy for epilepsy is represented by the transplantation of several types of cells such as mesenchymal stem cells (MSCs), bone marrow mononuclear cells, neural stem cells, and MSC-derived exosomes. Another approach is encapsulated cell biodelivery, which is the transplantation of genetically modified cells placed in capsules and secreting various therapeutic agents. The use of gene and cell therapy approaches can significantly improve the condition of patient with epilepsy. Therefore, preclinical, and clinical studies have been actively conducted in recent years to prove the benefits and safety of these strategies.

Indexed as

adeno-associated viruscell therapyencapsulated cell biodeliveryepilepsygene therapymesenchymal stem cellsmononuclear cellsneural stem cells

Identifiers

PMID35645733
PMCPMC9132249
OpenAlexW4280570640

What Socratic 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 Socratic graph.