Timo °Ã¤±è±è¾± - Liver Transplantation-associated Food Allergy and Eosinophilic Gastrointestinal Inflammation in Children - Clinical and Immunological Aspects
On October 28 Timo °Ã¤±è±è¾± is defending his thesis for Doctor of Medical 91̽»¨ at the Institute of Clinical 91̽»¨s, Sahlgrenska Academy, in the research subject of paediatric
The title of the thesis is: Liver Transplantation-associated Food Allergy and Eosinophilic Gastrointestinal Inflammation in Children - Clinical and Immunological Aspects
ABSTRACT
This thesis focuses on three recently described childhood-onset gastrointestinal disorders: liver transplantation-associated food allergy (LTFA), collagenous gastritis (CG) and eosinophilic esophagitis (EoE). Its aim was to gain additional understanding of both the clinical disease characteristics and the associated immunological aberrations in these conditions.
Study I investigated the frequencies of allergy, allergic sensitization as well as autoimmune disease and autoantibodies in a cross-sectional cohort of pediatric liver transplant recipients. The co-occurrence of food allergy and autoantibodies was found to be increased, indicating an underlying immune dysregulation that impairs immune tolerance to both food allergens and autoantigens in the affected individuals.
Study II analyzed serum cytokine concentrations and circulating lymphocyte subsets of the same patients who were included in Study I. Signs of ongoing immune activation were found to be prevalent despite clinically stable graft function. Additionally, the excessive underlying immune activation appeared to be associated with an increased susceptibility to develop LTFA.
Study III investigated the clinical disease course in childhood-onset CG. Further, CG was found to be associated with autoimmune predisposition and serum calprotectin and amyloid A was proposed as novel candidate biomarkers for monitoring the disease activity in CG.
Study IV involved analysis of blood eosinophil phenotype in children with active EoE. We found that these patients had a distinct molecular pattern of blood eosinophils compared with both healthy children and adults with active EoE.
The results of this thesis contribute to the improved clinical follow-up of the patients with the studied conditions. They also provide new insights into the associated immune deviations, which may facilitate the development of the future diagnostic and treatment options for these disorders.