Evidence map›Paper›PMID 41828614›Full record

SynthesisInternational journal of molecular sciences2026

Systematic Review: Preclinical and Clinical Evidence on MSC Efficacy and Mechanism of Action in Neuropathic Pain Reduction.

Zahrina Haziqah Harun, Min Hwei Ng, Nor Hazla Mohamed Haflah, Htwe Ohnmar, Yogeswaran Lokanathan, Zhe Kang Law, Amaramalar Selvi Naicker, Soon Yong Thow, Shalimar Abdullah

Abstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Zahrina Haziqah HarunDepartment of Orthopaedic & Traumatology, Faculty of Medicine, University Kebangsaan Malaysia, Jalan Yaacob Latif Kuala Lumpur, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.ORCID 0009-0005-1127-4650
Min Hwei NgDepartment of Tissue Engineering & Regenerative Medicine (DTERM), Faculty of Medicine, University Kebangsaan Malaysia, Jalan Yaacob Latif Kuala Lumpur, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.
Nor Hazla Mohamed HaflahDepartment of Orthopaedic & Traumatology, Faculty of Medicine, University Kebangsaan Malaysia, Jalan Yaacob Latif Kuala Lumpur, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.ORCID 0000-0002-5408-3943
Htwe OhnmarFaculty of Medicine, Universiti Sultan Zainal Abidin (UniSZA), Kuala Terengganu 20400, Malaysia.ORCID 0000-0001-6303-9859
Yogeswaran LokanathanDepartment of Tissue Engineering & Regenerative Medicine (DTERM), Faculty of Medicine, University Kebangsaan Malaysia, Jalan Yaacob Latif Kuala Lumpur, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.ORCID 0000-0002-9548-6490
Zhe Kang LawMedical Department, Faculty of Medicine, University Kebangsaan Malaysia, Jalan Yaacob Latif Kuala Lumpur, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.ORCID 0000-0002-7900-9037
Amaramalar Selvi NaickerDepartment of Orthopaedic & Traumatology, Faculty of Medicine, University Kebangsaan Malaysia, Jalan Yaacob Latif Kuala Lumpur, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.ORCID 0000-0002-5964-4930
Soon Yong ThowHospital Sultan Ismail, Jalan Mutiara Emas Utama, Taman Mount Austin, Johor Bahru 81100, Malaysia.
Shalimar AbdullahDepartment of Orthopaedic & Traumatology, Faculty of Medicine, University Kebangsaan Malaysia, Jalan Yaacob Latif Kuala Lumpur, Bandar Tun Razak, Cheras, Kuala Lumpur 56000, Malaysia.ORCID 0000-0003-4509-842X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nerve injury often results in neuropathic pain, marked by spontaneous pain, hyperalgesia, and allodynia. Current treatments have moderate efficacy and have side effects, prompting interest in alternative approaches. Mesenchymal stem cell (MSC) therapy has shown promise in preclinical studies for reducing neuropathic pain and inflammation. However, the precise mechanisms underlying MSC-mediated pain reduction remain unclear. Investigating these mechanisms is crucial for optimizing MSC-based therapies for neuropathic pain. This article provides a brief overview of the MSC administration, animal models of neuropathic pain, and treatment regimens used in 25 preclinical studies, focusing on the potential mechanisms of action underlying the neuropathic pain-reducing effect of MSCs. Importantly, 23 out of the 25 studies demonstrated a reduction in neuropathic pain following MSC therapy, despite differences in MSC sources and treatment regimens. Neuropathic pain relief was associated with decreased inflammation, suggesting that MSCs may act through immune modulation. However, the resolution of inflammation does not always correlate with complete neuropathic pain relief, indicating the involvement of additional mechanisms.

Indexed as

Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationNeuralgiaAnimalsDisease Models, AnimalHumansInflammationcell therapyimmunomodulationinflammationmesenchymal stem cellsneuropathic pain

Identifiers

PMID41828614
PMCPMC12985437

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.