Evidence map›Paper›PMID 42756695›Full record

ArticleMediterranean journal of rheumatology2026

CAR T-Cell Therapy in Systemic Lupus Erythematosus: Mechanistic Rationale, Early Clinical Experience, and Future Challenges.

Sabarinath Mahadevan, Saranya Chinnadurai, Balakrishnan Navaneethakrishnan

Abstract read
In one paragraph

Article in Mediterranean journal of rheumatology, 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

3 authors.

Sabarinath MahadevanInstitute of Rheumatology, MMC & RGGGH, Chennai, Tamilnadu, India.
Saranya ChinnaduraiDepartment of Rheumatology, Saveetha Medical College and Hospital, Chennai, Tamilnadu, India.
Balakrishnan NavaneethakrishnanConsultant Rheumatologist, St Thomas Hospital, Chethipuzha, Chenganaserry, Kerala, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) remains a challenging multisystem autoimmune disease characterised by relapses and remissions, often necessitating lifelong immunosuppression. Over the past decades, the therapeutic landscape has evolved from broad-spectrum agents such as cyclophosphamide to more targeted biologics including rituximab, belimumab, and anifrolumab-each contributing to incremental improvements in disease control. More recently, cell-based therapies have emerged as a novel strategy to reprogramme immune responses, including haematopoietic stem cell transplantation, bispecific T-cell engager (BiTE) therapy, and chimeric antigen receptor (CAR) T-cell therapy. CAR T-cell therapy represents a potentially transformative approach in SLE, offering the prospect of sustained clinical and immunological remission without ongoing immunosuppression. In this narrative review, we searched the Medline/PubMed, Scopus, Web of Science, and Directory of Open Access Journals (DOAJ) and included relevant original articles, clinical trials, randomised controlled trials, case studies and case reports published in the last 7 years. In this review, we discuss the mechanistic rationale for CAR T-cell therapy in SLE, review the clinical outcomes reported to date, and explore its promise in ushering a new era of durable, drug-free remission in autoimmune disease.

Indexed as

autoimmune diseaseschimericcytokine release syndromeimmunosuppressionlupusstem cell

Identifiers

PMID42756695
PMCPMC13583200

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.