# Year in Review: Axial Spondyloarthritis

**Authors:** Dimitrios Katsifis-Nezis, Antonis Fanouriakis

PMC · DOI: 10.31138/mjr.300925.era · 2026-01-08

## TL;DR

This review summarizes recent advancements in axial spondyloarthritis research from 2024–2025, covering immune mechanisms, imaging, and treatment.

## Contribution

Highlights novel immune mechanisms like IL-17 extracellular vesicles and CD8+ T cell responses, and advances in AI-based diagnosis and imaging.

## Key findings

- Novel immune stromal interactions, including IL-17 extracellular vesicles and IL-33-induced TREM2+ macrophages, were identified.
- Artificial intelligence models showed strong performance in early diagnosis and disease activity prediction.
- An international consensus on MRI protocols and the use of ultrasound for enthesitis assessment were established.

## Abstract

Axial spondyloarthritis is a chronic inflammatory disease primarily affecting the sacroiliac joints and spine. Over the past two years, significant progress has been made across multiple domains of spondyloarthritis research. The current review critically summarises key advancements in research during 2024–2025, covering pathophysiology, epidemiology, diagnosis, imaging, and clinical management. Notable findings include novel immune stromal interactions, such as IL-17 extracellular vesicles, IL-33 induced TREM2+ macrophages and disease specific CD8+ T cell responses that provide insight into bone remodelling and inflammation. Epidemiological data confirm persistent diagnostic delays, though targeted referral strategies show promise. Advances in imaging include an international consensus on MRI protocols and the growing use of ultrasound for the assessment of enthesitis. Artificial intelligence models demonstrate strong performance in early diagnosis, imaging interpretation and disease activity prediction and prognosis, while advances in therapy include the first head-to-head trial and numerous real-world data.

## Linked entities

- **Proteins:** IL17A (interleukin 17A), IL33 (interleukin 33), TREM2 (triggering receptor expressed on myeloid cells 2)

## Full-text entities

- **Genes:** CXCL12 (C-X-C motif chemokine ligand 12) [NCBI Gene 6387] {aka IRH, PBSF, SCYB12, SDF1, TLSF, TPAR1}, TREM2 (triggering receptor expressed on myeloid cells 2) [NCBI Gene 54209] {aka AD17, PLOSL2, TREM-2, Trem2a, Trem2b, Trem2c}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CD4 [NCBI Gene 101864991], IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, CD99 (CD99 molecule (Xg blood group)) [NCBI Gene 4267] {aka HBA71, MIC2, MIC2X, MIC2Y, MSK5X}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, IL17F (interleukin 17F) [NCBI Gene 112744] {aka CANDF6, IL-17F, ML-1, ML1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** nr- (MESH:D000089202), psoriasis (MESH:D011565), bone remodelling (MESH:D001847), oral candidiasis (MESH:D002180), depression (MESH:D003866), COVID-19 (MESH:D000086382), Bone marrow oedema (MESH:D004487), joint involvement (MESH:D007592), uveitis (MESH:D014605), Arthritis (MESH:D001168), intervertebral disc (MESH:C535531), anterior uveitis (MESH:D014606), AxSpA (MESH:D000089183), Psoriasis, Iritis, and Colitis (MESH:D007500), Buttock pain (MESH:D010146), SIJ inflammation (MESH:D007249), AS (MESH:D013167), Rheumatic Diseases (MESH:D012216), NSBP (MESH:D001416), ASAS (MESH:C000719191), degenerative disc disease (MESH:D055959), obesity (MESH:D009765), nasopharyngitis (MESH:D009304), DIAGNOSIS (MESH:D001523), hypertension (MESH:D006973), Enthesitis (MESH:D001171), spinal lesions (MESH:D013122), bone erosions (MESH:D014077), DISH (MESH:D004057), ARTIFICIAL INTELLIGENCE (MESH:C538142), RA (MESH:D001172), SIJ (MESH:C563037), CBP (MESH:D059350), IMAGING (MESH:C564543), autoinflammation (MESH:D056660), inflammatory bowel disease (MESH:D015212), ankylosis (MESH:D000844), low back pain (MESH:D017116), sacroiliitis (MESH:D058566), osteoporosis (MESH:D010024), fibromyalgia (MESH:D005356)
- **Chemicals:** certolizumab pegol (MESH:D000068582), tofacitinib (MESH:C479163), adalimumab (MESH:D000068879), ixekizumab (MESH:C549079), golimumab (MESH:C529000), celecoxib (MESH:D000068579), bimekizumab (MESH:C000625981), infliximab (MESH:D000069285), upadacitinib (MESH:C000613732), secukinumab (MESH:C555450), bDMARD (-)
- **Species:** Cercopithecidae (monkey, family) [taxon 9527], Homo sapiens (human, species) [taxon 9606], gut metagenome (species) [taxon 749906]

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Source: https://tomesphere.com/paper/PMC12835917