Evidence map›Paper›PMID 42890994›Full record

ReviewCureus2026

Chimeric Antigen Receptor T-cell (CAR-T) Therapy in Autoimmune Diseases: A Narrative Review.

Irviana A Molina-Garcia, Joselyn G Oliveros-Perez, Stephanie D Molina-Garcia, Anyuli P Guevara-Ostos, Maria F Blanco-Contreras, Ludwig M Camacho-Flores, Luisana S Rodriguez

Abstract readReview
In one paragraph

Review in Cureus, 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

7 authors.

Irviana A Molina-GarciaDentistry, University of the Andes, Mérida, VEN.
Joselyn G Oliveros-PerezGeneral Medicine, University of the Andes, Mérida, VEN.
Stephanie D Molina-GarciaGeneral Medicine, University of the Andes, Mérida, VEN.
Anyuli P Guevara-OstosGeneral Medicine, University of the Andes, Mérida, VEN.
Maria F Blanco-ContrerasGeneral Medicine, University of the Andes, Mérida, VEN.
Ludwig M Camacho-FloresGeneral Medicine, University of the Andes, Mérida, VEN.
Luisana S RodriguezDentistry, Universidad de Carabobo, Valencia, VEN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune diseases are chronic immune-mediated disorders that, in their systemic forms, such as systemic lupus erythematosus (SLE), systemic sclerosis (SSc), idiopathic inflammatory myopathies, and antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), remain associated with progressive organ damage, impaired quality of life, and excess mortality despite conventional immunosuppression. A substantial proportion of patients experience refractory disease, recurrent flares, and glucocorticoid dependence, underscoring the need for therapies that address the underlying disease process rather than merely suppressing symptoms. Chimeric antigen receptor T-cell (CAR-T) therapy, originally developed for B-cell malignancies, has emerged as a potential paradigm shift by achieving deep, tissue-level B-cell depletion followed by immune reconstitution, a process often described as an "immune reset." This narrative review summarizes the immunological rationale, clinical evidence, safety profile, and future directions of B-cell-directed (anti-CD19) CAR-T therapy in autoimmune disease. Current evidence identifies refractory SLE as the most mature indication, with reproducible drug-free remission, seroconversion, and durable responses across independent cohorts. Early studies in inflammatory myopathies and SSc report encouraging responses and reduced immunosuppressive requirements, whereas evidence in AAV remains preclinical. Toxicities such as cytokine release syndrome and neurotoxicity appear less frequent and less severe than in oncology, although infections and hypogammaglobulinemia require monitoring. High cost, complex manufacturing, and limited long-term data remain major barriers, while allogeneic CAR-natural killer cells and in vivo engineering may improve scalability. Larger controlled studies with longer follow-up are needed before routine clinical use.

Indexed as

allogeneic car-nk cellsautoimmune diseasesb-cell depletioncar-t cell therapyimmune resetsystemic lupus erythematosus

Identifiers

PMID42890994
PMCPMC13675094

What OpenQuestion holds

Textmetadata
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.