Evidence map›Paper›PMID 42008018›Full record

ReviewClinical reviews in allergy & immunology2026

The Evolving Landscape of CAR T-Cell Therapy in Autoimmune Diseases: A State-of-the-Art Review (2025).

Changpei Li, Hongjiang Liu, Shuyi Liao, Yifan Wang, Geng Yin, Qibing Xie

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical reviews in allergy & 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

6 authors.

Changpei LiDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Hongjiang LiuDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Shuyi LiaoDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Yifan WangDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Geng YinDepartment of General Practice, West China Hospital, General Practice Medical Center, Sichuan University, Chengdu, Sichuan, China. yingeng1975@163.com.
Qibing XieDepartment of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, China. xieqibing1971@163.com.

Funding

National Natural Science Foundation of China No. 82572070Postdoctor Research Fund of West China Hospital, Sichuan University No. 2024HXBH084Sichuan Province Science and Technology Department No. 2024YFFK0349, 2025ZNSFSC0638, 2024YFFK0062
6 · The paper itself

Abstract

Autoimmune diseases, characterized by a breakdown in immune tolerance and persistent autoantibody production, have traditionally been managed primarily through broad-spectrum immunosuppression. Chimeric antigen receptor (CAR) T-cell therapy, a groundbreaking modality once exclusive to oncology, has recently emerged as a transformative approach for treating autoimmunity. We conducted a comprehensive review and investigation into the applications of CAR T-cell therapy in distinct autoimmune diseases, mainly rheumatic diseases, exploring the full spectrum of CAR T modalities, including autologous, allogeneic, and the latest in vivo CAR T strategies. By combining preclinical studies with clinical evidence, we aim to elucidate the substantial potential of CAR T cells to achieve drug-free remission in autoimmune disorders through deep depletion of B cells and immune reset. Despite these promising outcomes from small cohorts or case studies, significant hurdles remain in the realms of safety and toxicity management, economic burden, complex manufacturing processes, and accessibility. In summary, this cross-disease and cross-platform review has thoroughly examined the current state of CAR T-cell therapy research for autoimmune diseases up to December 2025, providing updated insights and future perspectives on this transformative therapeutic strategy.

Indexed as

Autoimmune DiseasesImmunotherapy, AdoptiveReceptors, Chimeric AntigenT-LymphocytesAnimalsHumansReceptors, Antigen, T-CellReceptors, Antigen, T-CellReceptors, Chimeric AntigenAutoimmune diseasesB-cell depletionChimeric antigen receptor T-cell therapyImmune reset

Identifiers

PMID42008018

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.