Evidence map›Paper›PMID 41052891›Full record

ReviewRMD open2025

Key considerations for advancing chimeric antigen receptor (CAR) T-cell therapy for systemic lupus erythematosus (SLE): a multi-partner/disciplinary working group perspective.

Elena W Y Hsieh, James B Chung, Afsah Amin, Anca D Askanase, Beatrix Bartok, Paul Brunetta, Marlene J Carrasco-Alfonso, Cindy Coney, Jennifer C Cooper, Maria Dall'Era and 27 more

Abstract readReview
In one paragraph

Review in RMD open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. 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

37 authors.

Elena W Y Hsieh *Department of Immunology and Microbiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA lupusabc@lupusresearch.org.
James B Chung *Amgen Inc, Thousand Oaks, California, USA.
Afsah AminCenter for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.
Anca D AskanaseColumbia University Irving Medical Center, New York, New York, USA.
Beatrix BartokGilead Sciences Inc, Foster City, California, USA.
Paul BrunettaSana Biotechnology Inc, Seattle, Washington, USA.
Marlene J Carrasco-AlfonsoAstraZeneca, Boston, Massachusetts, USA.
Cindy ConeyLupus Voices Council, Lupus Research Alliance, New York, New York, USA.
Jennifer C CooperDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Maria Dall'EraUniversity of California San Francisco, San Francisco, California, USA.
Nikolay DelevBristol Myers Squibb Co, Princeton, New Jersey, USA.
Ann EldredAbbVie Inc, North Chicago, Illinois, USA.
Richard A FurieDivision of Rheumatology, Northwell Health, Great Neck, New York, USA.
Sandra GarcesBristol Myers Squibb Co, Princeton, New Jersey, USA.
Katie GrooverMichigan Lupus Foundation, Traverse City, Michigan, USA.
Monica HarringtonFluent in Science, LLC, New York, New York, USA.
Jonathan J HoganCabaletta Bio Inc, Philadelphia, Pennsylvania, USA.
Gavin H ImperatoCenter for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.
Meredith JacksonLupus Research Alliance, New York, New York, USA.ORCID 0009-0008-0673-6402
Shaun W JacksonCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, Washington, USA.
Artemio M JongcoGlaxoSmithKline, Philadelphia, Pennsylvania, USA.
Elaine KarisNkarta Inc, South San Francisco, California, USA.
Ashley KoegelBristol Myers Squibb Co, Princeton, New Jersey, USA.
Maximilian F KönigDivision of Rheumatology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Gary KoretzkyCornell University, Ithaca, New York, USA.
Vijay KumarCenter for Biologics Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.
Eric MorandSchool of Clinical Sciences, Monash University, Clayton, Victoria, Australia.ORCID 0000-0002-9507-3338
Aimee S PayneColumbia University Irving Medical Center, New York, New York, USA.
Vaishali PopatCenter for Biologics Research and Evaluation, US Food and Drug Administration, Silver Spring, Maryland, USA.
Naiyer RizviSynthekine Inc, Menlo Park, California, USA.
Patricia RohanDivision of Allergy, Immunology, and Transplantation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland, USA.
Michel SadelainColumbia University Irving Medical Center, New York, New York, USA.
Georg SchettDepartment of Medicine 3-Rheumatology and Immunology and Deutshes Zentrum Immuntherapie, Friedrich-Alexander-Universitat Erlangen-Nurnberg, Erlangen, BY, Germany.
Aman P SinghTakeda Pharmaceuticals America Inc, Cambridge, Massachusetts, USA.
Ronald F van VollenhovenDepartment of Rheumatology, Amsterdam University Medical Center, Amsterdam, Netherlands.ORCID 0000-0001-6438-8663
Debra ZackFate Therapeutics Inc, San Diego, California, USA.
Lupus ABC CAR T Working Group

Funding

Mechanistic insights into systemic lupus erythematosus (SLE) pathogenesis from inborn errors of immunityR01AR073938 · NIAMS · SEATTLE CHILDREN'S HOSPITAL · PI Shaun William Jackson · 2019 to 2026
$4.0M
Impact of Loss-of-function NADPH Oxidase Variants on B-Cell Activation in SLER01AR075813 · NIAMS · SEATTLE CHILDREN'S HOSPITAL · PI JACKSON, SHAUN WILLIAM · 2021 to 2025
$2.8M
Interrogating The Biology Of Human Lupus Nephritis Using Single Cell Resolution Spatial TranscriptomicsR01DK136980 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Shaun William Jackson · 2024 to 2026
$2.5M
Mentoring the next generation of researchers in pediatric autoimmunityK24AR085177 · NIAMS · SEATTLE CHILDREN'S HOSPITAL · PI Shaun William Jackson · 2025 to 2026
$424k
NIAMS NIH HHS K24 AR085177NIAMS NIH HHS R01 AR073938NIAMS NIH HHS R01 AR075813NIDDK NIH HHS R01 DK136980
6 · The paper itself

Abstract

Early data have shown the potential of chimeric antigen receptor (CAR) T-cell therapies to expand the therapeutic landscape in systemic lupus erythematosus (SLE). While many CAR T-cell therapy learnings can be drawn from the experience of this modality in oncology, key questions remain regarding clinical development considerations unique to lupus. To assess and discuss these issues, the Lupus Accelerating Breakthroughs Consortium, a public-private partnership, convened a multi-partner working group to collect the diverse perspectives of academics/clinicians (including rheumatologists and oncologists), industry representatives (including SLE as well as CAR T-cell clinical development experts), regulators and people living with lupus on this potentially ground-breaking therapy. The working group considered the risk/benefit considerations for eligibility criteria in lupus, early-phase dosing and dose-limiting toxicity challenges, incorporation of comparator arms in late-phase registrational trial design, SLE-specific issues in conditioning therapy and immune monitoring and the limitations of SLE pre-clinical models for studying cell therapies. The key future 'calls to action' for the field include the need for well-defined severity/refractoriness-based eligibility criteria, the need for long-term monitoring infrastructure and the need for educational and logistical support for rheumatologists and patients.

Indexed as

Immunotherapy, AdoptiveLupus Erythematosus, SystemicReceptors, Chimeric AntigenT-LymphocytesHumansReceptors, Chimeric AntigenBiological TherapyClinical TrialLupus Erythematosus, SystemicLupus NephritisT-Lymphocytes

Identifiers

PMID41052891
PMCPMC12506445

What OpenQuestion holds

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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.