Evaluation of the Sphingolipid Metabolite S1P as a Novel Biomarker in Food Allergy
Food allergies represent an increasing health concern in the industrialized countries and especially affect pediatric patients. In this population adverse reactions against food compounds can lead to anaphylactic reactions. Despite substantial research efforts, clinical markers predicting disease severity and symptoms are missing to date.
Recent studies have revealed that sphingolipids, especially sphingosine-1-phosphate (S1P), play an essential role in allergy. It was reported that asthmatic patients have higher S1P levels in bronchiallavage fluids after allergen challenge. First experimental studies revealed a correlation of S1P and the outcome of anaphylaxis. Furthermore, we have shown in our recent mouse study that S1P homeostasis is pivotal for food allergy induction and effector cell response. Therefore, it is the aim of the presented pilot project to evaluate whether S1P serum titers are altered in food allergic children and if the S1P levels correlate with the outcome of anaphylaxis during double blind placebo controlled food challenges (DBPCFCs).
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||The Role of Sphingosine-1-phosphate in Food Allergy - Biomarker for Disease Severity and Anaphylaxis Outcome|
- S1P in allergic and non-allergic patients before and after challenge [ Time Frame: up to 3 years ] [ Designated as safety issue: Yes ]The primary endpoint of this study is the measurement of S1P in allergic and non-allergic patients before and after challenge.
- Evaluation of allergic mediators and correlation with S1P levels [ Time Frame: up to 3 years ] [ Designated as safety issue: Yes ]Evaluation of allergic mediators like histamine, human mast cell tryptase and eosinophil cationic protein and correlate these results with the levels of S1P within the group and between allergic and non-allergic patients
Biospecimen Retention: Samples With DNA
whole blood, serum
|Study Start Date:||December 2011|
|Estimated Study Completion Date:||January 2016|
|Estimated Primary Completion Date:||January 2016 (Final data collection date for primary outcome measure)|
positive reaction during DBPCFC
no reaction during DBPCFC
|Contact: Zsolt Szépfalusi, MD||+43 1 40400 ext email@example.com|
|Contact: Susanne C. Diesner, MD, PhD||+43 1 firstname.lastname@example.org|
|Medical University Vienna, Department of Pediatrics and Adolescent Medicine||Recruiting|
|Vienna, Austria, 1090|
|Principal Investigator: Zsolt Szépfalusi, MD|
|Principal Investigator:||Eva Untersmayr-Elsenhuber, MD, PhD||Medical University Vienna, Department of Pathophysiology and Allergy Research|