# The clinical characteristics, mechanism and management of immune checkpoint inhibitor-related arthritis

**Authors:** Jian Gao, Jinlin Miao, Zhinan Chen, Ping Zhu

PMC · DOI: 10.3389/fimmu.2025.1611692 · Frontiers in Immunology · 2026-01-14

## TL;DR

This review explores arthritis caused by immune checkpoint inhibitors, its causes, symptoms, and treatment options to improve patient care.

## Contribution

The paper provides a comprehensive overview of the clinical features, mechanisms, and management of immune checkpoint inhibitor-related arthritis.

## Key findings

- Common rheumatic irAEs include arthralgia, mono-/oligo-/polyarthritis, and psoriatic arthritis.
- T cell dysregulation and cytokine-mediated inflammation are key mechanisms in irAE-arthritis.
- NSAIDs, corticosteroids, and JAK inhibitors are effective in managing irAE-arthritis.

## Abstract

Immune-related adverse events, notably arthritis (irAE-arthritis), frequently occur in patients receiving immune checkpoint inhibitors. Arthritis severity varies from mild to severe, adversely impacting quality of life. Despite reports in clinical trials and real-world studies, the pathophysiology and optimal management of irAE-associated arthritis (irAE-arthritis) are still unclear.

From the inception to September 25, 2025, a search was conducted on PubMed, EMBASE, and MEDLINE for case reports/series on irAE-arthritis.

The most common rheumatic irAEs were arthritis. Various rheumatic syndromes have been reported, such as arthralgia, mono-/oligo-/polyarthritis, reactive and psoriatic arthritis, RS3PE, tenosynovitis. The onset of irAE-arthritis is attributed to T cell dysregulation, B cell activation with autoantibody production, cytokine - mediated inflammation, and impaired immune tolerance due to Treg dysfunction. NSAIDs, intra-articular/systemic corticosteroids, csDMARDs, and biologics play key roles in irAE-arthritis management, and JAK inhibitors may emerge as a significant therapeutic strategy in the future.

Given the increasing use of immunotherapy in oncology and other fields, developing a comprehensive understanding of irAE-arthritis is crucial. This review aims to provide an in-depth overview of current knowledge on irAE-arthritis, including its epidemiology, clinical presentation, underlying mechanisms, and management approaches.

## Linked entities

- **Diseases:** arthritis (MONDO:0005578)

## Full-text entities

- **Diseases:** psoriatic arthritis (MESH:D015535), irAE-associated (MESH:D018886), rheumatic (MESH:D012216), inflammation (MESH:D007249), Arthritis (MESH:D001168), tenosynovitis (MESH:D013717), arthralgia (MESH:D018771)
- **Chemicals:** csDMARDs (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

141 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846936/full.md

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Source: https://tomesphere.com/paper/PMC12846936