Tissue exposure does not explain non-response in ulcerative colitis patients with adequate serum vedolizumab concentrations

Author(s):  
Nathalie Van den Berghe ◽  
Bram Verstockt ◽  
Ann Gils ◽  
João Sabino ◽  
Marc Ferrante ◽  
...  

Abstract Background and aims Some patients with ulcerative colitis (UC) do not respond to vedolizumab treatment despite adequate drug exposure in serum. This study aimed to investigate vedolizumab in tissue and questioned whether insufficient tissue exposure could explain non-response in UC patients with adequate serum vedolizumab concentrations. Methods A paired serum sample and colonic mucosal biopsy was collected from 40 UC patients (20 endoscopic responders, 20 non-responders) at week 14 of vedolizumab treatment. Vedolizumab, soluble (s)-mucosal addressin cell adhesion molecule-1 (MAdCAM-1), s-vascular cell adhesion molecule-1 (VCAM-1) and s-intercellular adhesion molecule-1 (ICAM-1) were measured in serum and/or tissue. Endoscopic response was defined as Mayo endoscopic sub-score ≤1. Results A significant positive correlation was observed between vedolizumab serum and colonic tissue concentrations (ρ = 0.84, p<0.0001), regardless of the macroscopic inflammatory state of the tissue. Vedolizumab tissue concentrations were lower in non-responders than in responders (0.07 vs 0.11 µg/mg, p = 0.04). In the subgroup of patients with adequate vedolizumab serum concentrations (>14.6 µg/mL), tissue vedolizumab was not significantly different between responders and non-responders (0.15 vs 0.13 µg/mg; p = 0.92). Serum sMAdCAM-1, but not serum sICAM-1 or sVCAM-1 concentrations, were significantly higher in responders than non-responders with adequate vedolizumab serum concentrations (1.04 vs 0.83 ng/mL, p =0.03). Conclusions Vedolizumab concentrations in colonic mucosal tissue of UC patients reflect the concentration in serum regardless of the macroscopic inflammatory state of the tissue. Our data shows that insufficient tissue exposure does not explain non-response in UC patients with adequate serum vedolizumab concentrations.

2018 ◽  
Vol 2 (1) ◽  
pp. e000312 ◽  
Author(s):  
Rens Zonneveld ◽  
Rianne M Jongman ◽  
Amadu Juliana ◽  
Grietje Molema ◽  
Matijs van Meurs ◽  
...  

BackgroundEarly onset sepsis (EOS) is defined as onset of sepsis within 72 hours after birth. Leucocyte-endothelial interactions play a pivotal part in EOS pathophysiology. Endothelial cell adhesion molecules (CAMs) orchestrate these interactions and their soluble isoforms (sCAMs) are released into the vasculature by enzymes called sheddases.PurposeThis study was undertaken to explore further the pathophysiology of EOS and to investigate the potential of sCAM and their sheddases as potential biomarkers for EOS.MethodsStored serum aliquots were used from 71 Surinamese newborns suspected of EOS and 20 healthy newborns from an earlier study. Serum had been collected within 72 hours after birth and six (8.6%) newborns had a positive blood culture with gram-negative pathogens. Concentrations of sCAMs sP-selectin, sE-selectin, soluble vascular cell adhesion molecule-1 , intercellular adhesion molecule-1 and platelet and endothelial cell adhesion molecule-1, sheddases matrix metalloproteinase-9 (MMP-9) and neutrophil elastase (NE) and sheddase antagonist tissue-inhibitor of metalloproteinases-1 (TIMP-1) were measured simultaneously with Luminex and ELISA.ResultsMMP-9 and TIMP-1 levels were measured in serum of n=91 newborns and sCAMs and NE levels in serum of n=80 newborns, respectively. We found no differences in median concentrations of sCAMs, MMP-9 and TIMP-1 or NE between blood culture positive EOS, blood culture negative EOS and control groups at start of antibiotic treatment.ConclusionsOur data indicate that serum concentrations of sCAMs and their sheddases have no clinical utility as biomarkers for EOS.Trial registration numberNCT02486783. Results


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