Dietary Factors and Mucosal Immune Response in Celiac Disease Patients Having Persistent Symptoms Despite a Gluten-free Diet.


Journal

Journal of clinical gastroenterology
ISSN: 1539-2031
Titre abrégé: J Clin Gastroenterol
Pays: United States
ID NLM: 7910017

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 6 3 2018
medline: 12 9 2020
entrez: 6 3 2018
Statut: ppublish

Résumé

The aim of this study was to investigate the role of dietary factors, distinct small-bowel mucosal immune cell types, and epithelial integrity in the perpetuation of gastrointestinal symptoms in treated celiac disease patients. For unexplained reasons, many celiac disease patients suffer from persistent symptoms, despite a strict gluten-free diet (GFD) and recovered intestinal mucosa. We compared clinical and serological data and mucosal recovery in 22 asymptomatic and 25 symptomatic celiac patients on a long-term GFD. The density of CD3 and γδ intraepithelial lymphocytes (IELs), CD25 and FOXP3 regulatory T cells, and CD117 mast cells, and the expression of tight junction proteins claudin-3 and occludin, heat shock protein 60, interleukin 15, and Toll-like receptor 2 and 4 were evaluated in duodenal biopsies. All subjects kept a strict GFD and had negative celiac autoantibodies and recovered mucosal morphology. The asymptomatic patients had higher mean fiber intake (20.2 vs. 15.2 g/d, P=0.028) and density of CD3 IELs (59.3 vs. 45.0 cell/mm, P=0.045) than those with persistent symptoms. There was a similar but nonsignificant trend in γδ IELs (17.9 vs. 13.5, P=0.149). There were no differences between the groups in other parameters measured. Low fiber intake may predispose patients to persistent symptoms in celiac disease. There were no differences between the groups in the markers of innate immunity, epithelial stress or epithelial integrity. A higher number of IELs in asymptomatic subjects may indicate that the association between symptoms and mucosal inflammation is more complicated than previously thought.

Sections du résumé

GOALS
The aim of this study was to investigate the role of dietary factors, distinct small-bowel mucosal immune cell types, and epithelial integrity in the perpetuation of gastrointestinal symptoms in treated celiac disease patients.
BACKGROUND
For unexplained reasons, many celiac disease patients suffer from persistent symptoms, despite a strict gluten-free diet (GFD) and recovered intestinal mucosa.
STUDY
We compared clinical and serological data and mucosal recovery in 22 asymptomatic and 25 symptomatic celiac patients on a long-term GFD. The density of CD3 and γδ intraepithelial lymphocytes (IELs), CD25 and FOXP3 regulatory T cells, and CD117 mast cells, and the expression of tight junction proteins claudin-3 and occludin, heat shock protein 60, interleukin 15, and Toll-like receptor 2 and 4 were evaluated in duodenal biopsies.
RESULTS
All subjects kept a strict GFD and had negative celiac autoantibodies and recovered mucosal morphology. The asymptomatic patients had higher mean fiber intake (20.2 vs. 15.2 g/d, P=0.028) and density of CD3 IELs (59.3 vs. 45.0 cell/mm, P=0.045) than those with persistent symptoms. There was a similar but nonsignificant trend in γδ IELs (17.9 vs. 13.5, P=0.149). There were no differences between the groups in other parameters measured.
CONCLUSIONS
Low fiber intake may predispose patients to persistent symptoms in celiac disease. There were no differences between the groups in the markers of innate immunity, epithelial stress or epithelial integrity. A higher number of IELs in asymptomatic subjects may indicate that the association between symptoms and mucosal inflammation is more complicated than previously thought.

Identifiants

pubmed: 29505551
doi: 10.1097/MCG.0000000000001013
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

507-513

Auteurs

Pilvi Laurikka (P)

Celiac Disease Research Center, Faculty of Medicine and Life Sciences.
Seinäjoki Central Hospital, Seinäjoki, Finland.

Katri Lindfors (K)

Celiac Disease Research Center, Faculty of Medicine and Life Sciences.

Mikko Oittinen (M)

Tampere Centre for Child Health Research, University of Tampere and Tampere University Hospital.

Heini Huhtala (H)

Faculty of Social Sciences.

Teea Salmi (T)

Departments of Dermatology.

Marja-Leena Lähdeaho (ML)

Tampere Centre for Child Health Research, University of Tampere and Tampere University Hospital.

Tuire Ilus (T)

Department of Gastroenterology and Alimentary Tract Surgery, Tampere University Hospital, Tampere.

Markku Mäki (M)

Tampere Centre for Child Health Research, University of Tampere and Tampere University Hospital.

Katri Kaukinen (K)

Celiac Disease Research Center, Faculty of Medicine and Life Sciences.
Internal Medicine, Tampere University Hospital, Faculty of Medicine and Life Sciences, University of Tampere.

Kalle Kurppa (K)

Tampere Centre for Child Health Research, University of Tampere and Tampere University Hospital.

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