# Anti-Integrin αvβ6 Autoantibodies Predict Response and Treatment Persistence to Advanced Therapies in Ulcerative Colitis

## TL;DR

This study shows that high levels of anti-integrin αvβ6 autoantibodies in ulcerative colitis patients predict poor response and early discontinuation of advanced therapies.

## Contribution

The study demonstrates that anti-αvβ6 autoantibody levels are a predictive biomarker for treatment outcomes in ulcerative colitis.

## Key findings

- High anti-αvβ6 autoantibody levels were associated with significantly lower treatment persistence.
- Low antibody levels predicted higher clinical remission rates at all measured time points.
- Low antibody levels remained an independent predictor of remission and treatment persistence.

## Abstract

Anti-integrin αvβ6 (anti-αvβ6) autoantibodies serve as a diagnostic biomarker and are associated with poor prognosis in ulcerative colitis (UC). We aimed to investigate whether anti-αvβ6 autoantibody levels predict treatment outcomes of advanced therapies in patients with moderately to severely active UC.

Anti-αvβ6 autoantibody levels were measured using prospectively collected serum samples at the initiation of advanced therapies. The primary outcome was treatment persistence up to 1 year; secondary outcomes included clinical remission rates at weeks 2, 6, 14, 24, and 48, comparing low-level and high-level groups stratified by an optimal cutoff from receiver operating characteristic analysis.

A total of 144 patients were analyzed (121 [84.0%] with extensive colitis and 87 [60.4%] with prior exposure to advanced therapies). The median observation period was 10 months, and treatment discontinuation occurred in 70 patients (48.6%). Treatment persistence was significantly higher in the low-level group (log-rank test, P = 0.002), and multivariable Cox analysis identified low antibody levels as the only independent predictor (hazard ratio, 1.90; 95% CI, 1.09–3.32). Clinical remission rates were consistently higher in the low-level group throughout all time points, with the greatest difference at week 6 (47.5% vs 20.0%; χ2 test, P = 0.003). Low antibody levels remained an independent predictor of remission at all time points.

Anti-αvβ6 autoantibodies predicted both treatment persistence and clinical remission after advanced therapies, highlighting their potential as a predictive biomarker in patients with active UC.