Could a genetic biomarker predict your risk for severe food allergies?

Researchers from Ann & Robert H. Lurie Children's Hospital of Chicago and colleagues reported for the first time that a genetic biomarker may help predict the severity of food allergy reactions. Currently, no reliable or readily available clinical biomarker accurately distinguishes patients with food allergies who are at risk for severe life-threatening reactions versus mild symptoms. Findings were published in the Journal of Allergy and Clinical Immunology.

Study: Severe food allergy reactions are associated with α-tryptase. Image Credit: Kaspars Grinvalds / Shutterstock

Dr. Lang and colleagues found that the presence of an enzyme isoform called α-tryptase, encoded by the TPSAB1 gene, correlates with an increased prevalence of anaphylaxis or severe reaction to food compared to subjects without any α-tryptase.

"Determining whether or not a patient with food allergies has α-tryptase can easily be done in clinical practice using a commercially available test to perform genetic sequencing from cheek swabs," said lead author Abigail Lang, MD, MSc, attending physician and researcher at Lurie Children's and Assistant Professor of Pediatrics at Northwestern University Feinberg School of Medicine. "If the biomarker is detected, this may help us understand that the child is at a higher risk for a severe reaction or anaphylaxis from their food allergy and should use their epinephrine auto-injector if exposed to the allergen. Our findings also open the door to developing an entirely new treatment strategy for food allergies that would target or block α-tryptase. This is an exciting first step and more research is needed."

Tryptase is found mainly in mast cells, which are white blood cells that are part of the immune system. Mast cells become activated during allergic reactions. Increased TPSAB1 copy number, which leads to increased α-tryptase, is already known to be associated with severe reactions in adults with Hymenoptera venom allergy (or anaphylaxis following a bee sting).

Dr. Lang's study included 119 participants who underwent TPSAB1 genotyping, 82 from an observational food allergy cohort at the National Institute of Allergy and Infectious Diseases (NIAID), and 37 from a cohort of children who reacted to peanut oral food challenge at Lurie Children's.

"We need to validate our preliminary findings in a much larger study, but these initial results are promising," says Dr. Lang. "We also still need a better understanding of why and how α-tryptase makes food allergy reactions more severe in order to pursue this avenue for potential treatment."

Rajesh Kumar, MD, MSc, from Lurie Children's, is the study's co-senior author. Dr. Kumar is the Interim Division Head of Allergy and Immunology and Professor of Pediatrics at Northwestern University Feinberg School of Medicine.

This work was partly supported by the Midwest Allergy Research Institute (MARI) Food Allergy Pilot Research Award and NIAID-sponsored T32 grant AI083216. This project was partially funded with federal funds from the Division of Intramural Research of the National Institute of Allergy and Infectious Diseases, NIH. This project has also been funded in whole or in part with federal funds from the National Cancer Institute, National Institutes of Health, under Contract No. 75N91019D00024.