# Potential benefits of JAK inhibitor therapy in Blau syndrome: a case report

**Authors:** Yu Wang, Xiao-juan Yu, Zhuoli Zhang

PMC · DOI: 10.3389/fimmu.2025.1665949 · Frontiers in Immunology · 2026-01-12

## TL;DR

A patient with Blau syndrome showed improved kidney function after treatment with the JAK inhibitor baricitinib, suggesting it may be an effective therapy for this rare inflammatory disorder.

## Contribution

This case report highlights baricitinib as a potential treatment for Blau syndrome, particularly in cases with renal involvement.

## Key findings

- Baricitinib rapidly normalized renal function in a Blau syndrome patient with granulomatous nephritis.
- JAK inhibition may offer advantages over TNF-α inhibitors in managing Blau syndrome.
- The p.R334W NOD2 mutation in this case caused constitutive NF-κB activation and excessive cytokine production.

## Abstract

Blau syndrome is a rare autoinflammatory disorder caused by gain-of-function mutations in the NOD2 (nucleotide binding oligomerization domain containing 2 receptor) gene. Blau Syndrome presents with the diagnostic triad of chronic polyarticular synovitis, recurrent uveitis, and dermatitis. Notably, patients often develop systemic granulomatous inflammation affecting multiple organs, particularly the kidney and liver. Here we report a case of Blau syndrome presented with early-onset arthritis, uveitis, and renal involvement, evidenced by granulomas tubulointerstitial nephritis. Genetic testing showed a pathogenic p.R334W NOD2 mutation demonstrating constitutive NF-κB activation and excessive proinflammatory cytokine production. While initial corticosteroid therapy improved articular and ocular symptoms, renal dysfunction persisted until baricitinib (4 mg/day) initiation, which rapidly normalized renal function and permitted steroid tapering. Granulomatous inflammation in Blau syndrome is mediated by IFN-γ and sustained JAK-STAT activation, making JAK1/2 inhibition a rational therapeutic target. Although TNF-α inhibitors show efficacy in some cases, our experience supports baricitinib’s potential for refractory disease, particularly with renal involvement. Baricitinib can offer distinct advantages over biologics and effectively downregulates inflammation in Blau syndrome.

## Linked entities

- **Genes:** NOD2 (nucleotide binding oligomerization domain containing 2) [NCBI Gene 64127]
- **Proteins:** NFKB1 (nuclear factor kappa B subunit 1), IFNG (interferon gamma)
- **Chemicals:** baricitinib (PubChem CID 44205240)
- **Diseases:** Blau syndrome (MONDO:0008523), tubulointerstitial nephritis (MONDO:0001085)

## Full-text entities

- **Genes:** NOD2 (nucleotide binding oligomerization domain containing 2) [NCBI Gene 64127] {aka ACUG, BLAU, BLAUS, CARD15, CD, CLR16.3}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** renal involvement (MESH:C565423), dermatitis (MESH:D003872), granulomas (MESH:D006099), autoinflammatory disorder (MESH:D056660), chronic polyarticular synovitis (MESH:D013585), uveitis (MESH:D014605), tubulointerstitial nephritis (MESH:D009395), Blau Syndrome (MESH:C538157), Granulomatous inflammation (MESH:D007249), renal dysfunction (MESH:D007674), arthritis (MESH:D001168)
- **Chemicals:** Baricitinib (MESH:C000596027), steroid (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** p.R334W

## Full text

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## Figures

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832996/full.md

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Source: https://tomesphere.com/paper/PMC12832996