# Case Report: Successful management of refractory SAPHO syndrome with guselkumab-upadacitinib combination

**Authors:** Di Jin, Ming Yuan Xu, Xiao Li Wang, Ruo Qi Wang, Jun Ting Tang, Ye Qiang Liu

PMC · DOI: 10.3389/fimmu.2026.1745464 · Frontiers in Immunology · 2026-02-20

## TL;DR

A 38-year-old man with severe SAPHO syndrome found relief through a new drug combination, offering hope for similar difficult cases.

## Contribution

This is the first report of guselkumab and upadacitinib combination achieving remission in refractory SAPHO syndrome.

## Key findings

- Complete pain resolution occurred within 2 weeks of treatment.
- Cutaneous lesions improved significantly within 4 weeks.
- The treatment showed a favorable safety profile during follow-up.

## Abstract

SAPHO syndrome is a rare chronic aseptic inflammatory disorder characterized by the concurrence of osteoarticular inflammation and cutaneous lesions. The intricate mechanism network, coupled with issues such as paradoxical reactions, often results in suboptimal therapeutic outcomes. To the best of our knowledge, this is the first report of refractory SAPHO syndrome achieving clinical remission with the combination of guselkumab (an IL-23 inhibitor) and upadacitinib (a JAK inhibitor). A 38-year-old male with refractory SAPHO experienced complete pain resolution within 2 weeks and significant improvement in cutaneous lesions by 4 weeks post-treatment, with a favorable safety profile observed throughout the follow-up period. We further analyzed the underlying inflammatory mechanisms to provide a therapeutic clues for the management of similar refractory cases.

## Linked entities

- **Chemicals:** upadacitinib (PubChem CID 58557659)
- **Diseases:** SAPHO syndrome (MONDO:0019266)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, JAK1 (Janus kinase 1) [NCBI Gene 3716] {aka AIIDE, JAK1A, JAK1B, JTK3}
- **Diseases:** rashes (MESH:D005076), onychomatrix opacity (MESH:D003318), SAPHO (MESH:D020083), cutaneous lesions (MESH:D009059), chest/back pain (MESH:D002637), Malassezia folliculitis (MESH:D005499), psoriatic arthritis (MESH:D015535), osteoarticular (MESH:D014394), palmoplantar pustulosis (MESH:D011565), cartilage (MESH:D002357), inflammation (MESH:D007249), morning stiffness (MESH:D048968), telangiectasia (MESH:D013684), pain (MESH:D010146), Skin Disease (MESH:D012871), ECT (MESH:D019305), tumoral conditions (MESH:D009369), pigmentation (MESH:D010859), bone marrow edema (MESH:D004487), joint tenderness (MESH:D063806), osteomyelitis (MESH:D010019), movement limitation (MESH:D045745), plantar pustules (MESH:D016523), acne (MESH:D000152), erythema (MESH:D004890), parakeratosis (MESH:D010241), hyperostosis (MESH:D015576), arthritis (MESH:D001168), cutaneous symptoms (MESH:D012816), palmoplantar pustules (MESH:D007645), infection (MESH:D007239), immune dysfunction (MESH:D007154), Synovitis (MESH:D013585), Bone-joint involvement (MESH:D001847), aseptic (MESH:D008582), Infectious osteitis (MESH:D010000), pain of sacroiliitis (MESH:D058566)
- **Chemicals:** methotrexate (MESH:D008727), secukinumab (MESH:C555450), risankizumab (MESH:C000601773), etoricoxib (MESH:D000077613), Upadacitinib (MESH:C000613732), ustekinumab (MESH:D000069549), selenium disulfide (MESH:C025698), steroids (MESH:D013256), halometasone (MESH:C036518), DAMPs (MESH:C116255), bisphosphonates (MESH:D004164), folate (MESH:D005492), IL-1 antagonists (-), Guselkumab (MESH:C000588857)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963310/full.md

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Source: https://tomesphere.com/paper/PMC12963310