High endothelial venules associated with T cell subsets in the inflamed gut of newly diagnosed inflammatory bowel disease patients
Author(s) -
Horjus Talabur Horje C. S.,
Smids C.,
Meijer J. W. R.,
Groenen M. J.,
Rijnders M. K.,
van Lochem E. G.,
Wahab P. J.
Publication year - 2017
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.12918
Subject(s) - addressin , medicine , high endothelial venules , inflammatory bowel disease , ulcerative colitis , lymphocyte homing receptor , interquartile range , gastroenterology , pathology , population , immunology , t cell , lymphatic system , disease , immune system , cell , biology , integrin , cell adhesion , genetics , receptor , environmental health
Summary Naive and central memory T lymphocytes (T N and T CM ) can infiltrate the inflamed gut mucosa in inflammatory bowel disease (IBD) patients. Homing of these subsets to the gut might be explained by ectopic formation of tertiary lymphoid organs (TLOs), containing high endothelial venules (HEVs). We aimed to evaluate the presence of HEVs and TLOs in inflamed intestinal mucosa of newly diagnosed, untreated IBD patients in relation to the presence of T N and T CM lymphocytes. IBD patients ( n = 39) and healthy controls ( n = 8) were included prospectively. Biopsy samples of inflamed and normal intestine, respectively, were analysed by immunohistochemistry for lymphocytes (CD3/CD20), blood vessels (CD31) and peripheral lymph node addressin (PNAd) expression (MECA‐79). T N and T CM lymphocyte subsets were identified by flow cytometric immunophenotyping. A higher number of HEVs was found in the inflamed colon of patients with ulcerative colitis [median 3·05 HEV/mm 2 ; interquartile range (IQR) = 0–6·39] and ileum of Crohn's disease patients (1·40; 0‐4·34) compared to healthy controls (both 0; P = 0·033). A high density of colonic HEVs (HEV high ) was associated with increased infiltration of T N and T CM in the inflamed gut (median 87%; IQR = 82–93% of T cell population), compared to HEV low patients (58%; 38–81%; P = 0·003). The number of colonic follicles was higher in HEV high patients (median 0·54/mm 2 ; IQR 0·28–0·84) compared to HEV low patients (0·25/mm 2 ; 0·08–0·45; P = 0·031) and controls (0·31/mm 2 ; 0·23–0·45; P = 0·043). Increased homing of T N and T CM lymphocytes to inflamed gut tissue in IBD patients might be facilitated by ectopic formation of extrafollicular HEVs and TLOs in a subgroup of patients.
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