# From myth to bedside: a scoping review of the applications of the chimeric antigen receptor in rheumatology

**Authors:** Diego Niño-Torres, Gerardo Quintana-López, Gustavo Salguero

PMC · DOI: 10.1007/s10238-025-01717-9 · Clinical and Experimental Medicine · 2025-06-06

## TL;DR

This review explores the use of chimeric antigen receptor therapies in treating autoimmune rheumatic diseases, highlighting promising early results and ongoing clinical trials.

## Contribution

The paper provides a comprehensive scoping review of CAR therapies in rheumatology, identifying current targets and cell types used in these treatments.

## Key findings

- CAR-T against CD19 is the most used type in rheumatology with good preliminary results.
- Other CAR targets include BCMA, PD-1, modified HLA, and citrullinated peptides.
- Natural killer and regulatory T cells are also being explored as CAR-based therapies.

## Abstract

Chimeric antigen receptor (CAR) based therapies are promising in systemic autoimmune rheumatic disease (SARD) according to recent case reports. To establish the state of the art of the applications of CAR therapies in rheumatology, PubMed, EMBASE, Lilacs, as well as clinical trial registries were searched. Any type of original article that reported the use of these therapies in patients with SARD was included. Forty-eight studies were included from databases. Ninety-five ongoing trials were included from clinical trials registries. The most used type of CAR was a CAR-T against CD19, showing good preliminary results. Other targets used were BCMA, PD-1, a modified HLA and citrullinated peptides among others. The use of other cell types such as natural killer and regulatory T cells was also found. CAR-based therapies in rheumatology are in an early stage of development but with promising results. There has been a notable growth in human patients treated with this intervention in the last 2 years. This and other innovative designs will offer a wide range of new therapeutic possibilities. Results of ongoing clinical trials are needed to establish their efficacy and safety in SARD.

The online version contains supplementary material available at 10.1007/s10238-025-01717-9.

## Linked entities

- **Proteins:** CD19 (CD19 molecule), TNFRSF17 (TNF receptor superfamily member 17), PDCD1 (programmed cell death 1)

## Full-text entities

- **Genes:** HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, NR1I3 (nuclear receptor subfamily 1 group I member 3) [NCBI Gene 9970] {aka CAR, CAR1, MB67}, TNFRSF17 (TNF receptor superfamily member 17) [NCBI Gene 608] {aka BCM, BCMA, CD269, TNFRSF13A}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** SARD (MESH:D012216)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12144057/full.md

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Source: https://tomesphere.com/paper/PMC12144057