Evidence map›Paper›PMID 38785982›Full record

ReviewBiomolecules2024

Chimeric Cell Therapies as a Novel Approach for Duchenne Muscular Dystrophy (DMD) and Muscle Regeneration.

Katarzyna Budzynska, Maria Siemionow, Katarzyna Stawarz, Lucile Chambily, Krzysztof Siemionow

Abstract readReview
In one paragraph

Review in Biomolecules, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Progress on cell therapy for skeletal muscle disorders.Advanced drug delivery reviews · 2026
    Review
  2. Article
  3. Article
  4. 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

5 authors.

Katarzyna BudzynskaDepartment of Orthopaedics, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0009-0001-9150-9974
Maria SiemionowDepartment of Orthopaedics, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0000-0001-6372-6122
Katarzyna StawarzDepartment of Orthopaedics, University of Illinois at Chicago, Chicago, IL 60607, USA.
Lucile ChambilyDepartment of Orthopaedics, University of Illinois at Chicago, Chicago, IL 60607, USA.ORCID 0009-0008-3377-3284
Krzysztof SiemionowDepartment of Orthopaedics, University of Illinois at Chicago, Chicago, IL 60607, USA.

Funding

Polish-American Medical Society in Chicago (PAMS) 2023The Kosciuszko Foundation (KF) Special Grant 2023
6 · The paper itself

Abstract

Chimerism-based strategies represent a pioneering concept which has led to groundbreaking advancements in regenerative medicine and transplantation. This new approach offers therapeutic potential for the treatment of various diseases, including inherited disorders. The ongoing studies on chimeric cells prompted the development of Dystrophin-Expressing Chimeric (DEC) cells which were introduced as a potential therapy for Duchenne Muscular Dystrophy (DMD). DMD is a genetic condition that leads to premature death in adolescent boys and remains incurable with current methods. DEC therapy, created via the fusion of human myoblasts derived from normal and DMD-affected donors, has proven to be safe and efficacious when tested in experimental models of DMD after systemic-intraosseous administration. These studies confirmed increased dystrophin expression, which correlated with functional and morphological improvements in DMD-affected muscles, including cardiac, respiratory, and skeletal muscles. Furthermore, the application of DEC therapy in a clinical study confirmed its long-term safety and efficacy in DMD patients. This review summarizes the development of chimeric cell technology tested in preclinical models and clinical studies, highlighting the potential of DEC therapy in muscle regeneration and repair, and introduces chimeric cell-based therapies as a promising, novel approach for muscle regeneration and the treatment of DMD and other neuromuscular disorders.

Indexed as

Cell- and Tissue-Based TherapyDystrophinMuscle, SkeletalMuscular Dystrophy, DuchenneRegenerationAnimalsHumansMyoblastsDystrophincellular therapychimeric cellschimerismDEC therapydonor-recipient chimeric cellsDuchenne Muscular DystrophyDystrophin Expressing Chimeric (DEC) cellsmuscle regenerationstem cells

Identifiers

PMID38785982
PMCPMC11117592

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.