Evidence map›Paper›PMID 39882532›Full record

ReviewFrontiers in medicine2024

Cell therapy for scleroderma: progress in mesenchymal stem cells and CAR-T treatment.

Liting Chen, Rongshan Huang, Chaoshuo Huang, Guiming Nong, Yuanyuan Mo, Lvyin Ye, Kunhong Lin, Anping Chen

Abstract readReview
In one paragraph

Review in Frontiers in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. 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

8 authors.

Liting ChenDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.
Rongshan HuangDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.
Chaoshuo HuangDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.
Guiming NongDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.
Yuanyuan MoDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.
Lvyin YeDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.
Kunhong LinDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.
Anping ChenDepartment of Rheumatology and Immunology, Qinzhou First People's Hospital, Qinzhou, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell therapy is an emerging strategy for precision treatment of scleroderma. This review systematically summarizes the research progress of mesenchymal stem cell (MSC) and chimeric antigen receptor T cell (CAR-T) therapies in scleroderma and discusses the challenges and future directions for development. MSCs possess multiple functions, including immunomodulation, anti-fibrosis, and promotion of vascular regeneration, all of which can improve multiple pathological processes associated with scleroderma. Studies have demonstrated that MSCs can alleviate skin fibrosis by inhibiting CCL2 production and reducing the recruitment of pathological macrophages; their paracrine effects can exert extensive regulatory functions. CAR-T cell therapy ca specifically target and eliminate autoreactive immune cells, exhibiting enhanced specificity and personalized potential. Different cell therapies may have complementary and synergistic effects in treating scleroderma, such as MSCs exerting their effects through paracrine mechanisms while CAR-T cells specifically eliminate pathological cells. Furthermore, cell-free therapies derived from MSCs, such as extracellular vesicles or exosomes, may help circumvent the limitations of MSC therapy. Although cell therapy has opened new avenues for the precision treatment of scleroderma, it still faces numerous challenges. In the future, it is essential to strengthen integration of basic and clinical research, establish standardized protocols for cell preparation and quality control, develop personalized treatment plans, and rationally combine cell therapy with existing treatment methods to maximize its advantages and improve patient prognosis and quality of life.

Indexed as

cell therapychimeric antigen receptor T cellsmesenchymal stem cell exosomesmesenchymal stem cellsscleroderma

Identifiers

PMID39882532
PMCPMC11774712

What OpenQuestion holds

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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.