Evidence map›Paper›PMID 42851527›Full record

ReviewFrontiers in immunology2026

When too late is too late: timing of CAR T-cell therapy in SLE & lupus nephritis.

Saira Sheikh, Shaun Jackson, Vimal Derebail, Natalie Grover, Astia Allenzara

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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

5 authors.

Saira SheikhSchool of Medicine, Department of Medicine, Division of Rheumatology, Allergy and Immunology & University of North Carolina (UNC) Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Shaun JacksonDepartment of Pediatrics, University of Washington School of Medicine, Seattle, WA, United States.
Vimal DerebailSchool of Medicine, Department of Medicine, Division of Nephrology and Hypertension and University of North Carolina (UNC) Kidney Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Natalie GroverSchool of Medicine, Department of Medicine, Division of Hematology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Astia AllenzaraSchool of Medicine, Department of Medicine, Division of Rheumatology, Allergy and Immunology & University of North Carolina (UNC) Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CAR T-cell therapy has demonstrated the capacity to induce deep, drug-free remissions in patients with severe, refractory systemic lupus erythematosus (SLE), including those with lupus nephritis (LN). These observations challenge long-standing assumptions about the reversibility of autoimmune disease and raise a critical question: whether CAR T-cell therapy should remain a therapy of last resort or if trials could investigate use earlier in the disease course, when its disease-modifying potential may be greatest. When CAR T-cell therapy is administered late in the disease course, its true biologic effect may therefore be underestimated, and clinical nonresponse may be misattributed to lack of therapeutic activity rather than to persistent damage and fibrosis. CAR T-cell therapy is still experimental and undergoing investigation as a treatment option in autoimmune diseases. Given the potential for a durable disease-free, drug free remission, we propose investigating use of CAR T-cell therapy in early severe SLE. We highlight CAR T-cell therapy in SLE and LN with a brief discussion of risks and benefits from the evidence to date. The current positioning as a refractory/salvage therapy late in the treatment algorithm may limit its impact for patients with SLE at high risk of irreversible organ damage.

Indexed as

Immunotherapy, AdoptiveLupus Erythematosus, SystemicLupus NephritisReceptors, Chimeric AntigenT-LymphocytesAnimalsHumansTime FactorsTreatment OutcomeReceptors, Chimeric Antigencell therapychimeric antigen receptor (CAR T)clinical trialslupus nephritislupus (SLE)treatment

Identifiers

PMID42851527
PMCPMC13646173

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.