Evidence map›Paper›PMID 42812406›Full record

ReviewJournal of rheumatic diseases2026

Chimeric Antigen Receptor T-cell therapy in systemic lupus erythematosus and other autoimmune diseases: a literature review.

Faryal Razzaq, Rana Uzair Ahmad, Ahmad Iftikhar, Farva Gondal, Mohammad Ebad Ur Rehman, Muhammad Suhaib, Muhammad Seerat Ali, Ernest Vina, Muhammad Husnain

Abstract readReview
In one paragraph

Review in Journal of rheumatic diseases, 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.

Faryal RazzaqDivision of Rheumatology, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0000-0003-4300-0740
Rana Uzair AhmadDepartment of Medicine, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0000-0002-3258-8676
Ahmad IftikharDepartment of Medicine, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0000-0002-2358-7057
Farva GondalDivision of Rheumatology, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0009-0006-5869-6321
Mohammad Ebad Ur RehmanDepartment of Medicine, Rawalpindi Medical University, Rawalpindi, Pakistan.ORCID https://orcid.org/0000-0001-8118-4849
Muhammad SuhaibDepartment of Medicine, Allama Iqbal Medical College, Lahore, Pakistan.ORCID https://orcid.org/0000-0001-6705-2030
Muhammad Seerat AliDepartment of Medicine, Quaid-e-Azam Medical College, Bahawalpur, Pakistan.ORCID https://orcid.org/0009-0000-6714-6985
Ernest VinaDivision of Rheumatology, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0000-0001-8135-1731
Muhammad HusnainDivision of Hematology & Oncology, University of Arizona, Tucson, AZ, USA.ORCID https://orcid.org/0000-0001-7248-9835

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune diseases such as systemic lupus erythematosus (SLE), arise when the immune system inappropriately attacks the body's own tissues, leading to chronic inflammation and significant morbidity. Traditional treatments, including corticosteroids, immunosuppressive drugs, and biologic agents, often provide incomplete disease control and are associated with substantial side effects. Chimeric Antigen Receptor (CAR) T-cell therapy, which targets and eliminates autoreactive B cells, has emerged as a promising novel approach for these conditions. This review evaluates the efficacy, safety, and therapeutic potential of CAR T-cell therapy in SLE and other autoimmune diseases, focusing on recent the most recent clinical studies. The review shows significant clinical improvements and sustained remissions in patients with severe, refractory autoimmune conditions, particularly with CD19 and B Cell Maturation Antigen (BCMA)-targeted CAR T-cell preparations. The review also examines adverse effects and safety profiles, emphasizing the differences in toxicity between cancer patients and those with autoimmune diseases. Overall, the findings highlight the transformative potential of CAR T-cell therapy in autoimmune diseases management, offering new possibilities for more effective and longer-lasting disease control while underscoring the need for further research to optimize therapy protocols and better understand long-term outcomes and safety.

Indexed as

Autoimmune diseaseChimeric Antigen Receptor T-cell therapySystemic lupus erythematosus

Identifiers

PMID42812406
PMCPMC13619548

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.