P015 PNAd+ and MAdCAM+ high endothelial venules correlate with disease activity in ulcerative colitis

2019 ◽  
Vol 13 (Supplement_1) ◽  
pp. S093-S094
Author(s):  
B Roosenboom ◽  
P Wahab ◽  
J Meijer ◽  
C Smids ◽  
M Groenen ◽  
...  
Cells ◽  
2020 ◽  
Vol 9 (4) ◽  
pp. 891
Author(s):  
Britt Roosenboom ◽  
Ellen G. van Lochem ◽  
Jos Meijer ◽  
Carolijn Smids ◽  
Stefan Nierkens ◽  
...  

PNAd and MAdCAM-1 addressins on venules are of importance in T-cell homing and potential therapeutic targets in ulcerative colitis (UC). Normally, PNAd+ high endothelial venules (HEVs) are only present in lymphoid organs, whereas small numbers of MAdCAM-1+ venules can be seen in non-lymphoid tissue. We aimed to study their presence in the intestinal mucosa of UC patients at diagnosis and during follow-up, and their correlation with disease activity. Colonic biopsy specimens of 378 UC patients were analyzed by immunohistochemistry for CD3, CD20, ERG, MECA-79 (PNAd) and MECA-376 (MAdCAM-1) and compared to healthy controls (HC). The proportion of PNAd+HEVs in UC at diagnosis was 4.9% (IQR 2.0%–8.3%), while none were detected in HC. During follow-up, PNAd+HEVs completely disappeared in remission (n = 93), whereas the proportion in active disease was similar to baseline (n = 285, p = 0.39). The proportion of MAdCAM-1+venules in UC at baseline was 5.8% (IQR 2.6–10.0). During follow-up, the proportion in remission was comparable to diagnosis, but upregulated (7.5% (IQR 4.4–10.9), p = 0.001) in active disease. In conclusion, PNAd+HEVs appear in UC during active inflammation which could thus serve as a marker for disease activity, whereas MAdCAM-1+venules remain present after inflammation is resolved and increase after subsequent flares, reflecting chronicity and potentially serving as a therapeutic target.


2018 ◽  
Vol 154 (1) ◽  
pp. S58
Author(s):  
Salah Badr El-Din ◽  
Ezzat Ali ◽  
Doaa Header ◽  
Pacint Moez ◽  
Mohamed Ibrahim

2009 ◽  
Vol 47 (09) ◽  
Author(s):  
M Jürgens ◽  
R Laubender ◽  
F Hartl ◽  
M Weidinger ◽  
J Wagner ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lena Öhman ◽  
Anders Lasson ◽  
Anna Strömbeck ◽  
Stefan Isaksson ◽  
Marcus Hesselmar ◽  
...  

AbstractPatients with ulcerative colitis (UC) have an altered gut microbiota composition, but the microbial relationship to disease activity needs to be further elucidated. Therefore, temporal dynamics of the fecal microbial community during remission and flare was determined. Fecal samples were collected at 2–6 time-points from UC patients during established disease (cohort EST) and at diagnosis (cohort NEW). Sampling range for cohort EST was 3–10 months and for cohort NEW 36 months. Relapses were monitored for an additional three years for cohort EST. Microbial composition was assessed by Genetic Analysis GA-map Dysbiosis Test, targeting ≥ 300 bacteria. Eighteen patients in cohort EST (8 with maintained remission and 10 experiencing a flare), provided 71 fecal samples. In cohort NEW, 13 patients provided 49 fecal samples. The microbial composition showed no clustering related to disease activity in any cohort. Microbial dissimilarity was higher between than within patients for both cohorts, irrespective of presence of a flare. Microbial stability within patients was constant over time with no major shift in overall composition nor modification in the abundance of any specific species. Microbial composition was not affected by intensified medical treatment or linked to future disease course. Thus in UC, the gut microbiota is highly stable irrespective of disease stage, disease activity or treatment escalation. This suggests that prolonged dietary interventions or repeated fecal transplantations are needed to be able to induce permanent alterations of the gut microbiota.


Life Sciences ◽  
2021 ◽  
Vol 269 ◽  
pp. 119077
Author(s):  
Guohui Xue ◽  
Lin Hua ◽  
Dongsheng Liu ◽  
Meijun Zhong ◽  
Yuanwang Chen ◽  
...  

2015 ◽  
Vol 42 (8) ◽  
pp. 957-967 ◽  
Author(s):  
A. Marchal Bressenot ◽  
R. H. Riddell ◽  
C. Boulagnon-Rombi ◽  
W. Reinisch ◽  
S. Danese ◽  
...  

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