About 25 million people in the United States—seven million of them children—suffer from asthma. A five-year, $7 million National Institutes of Health (NIH) grant awarded recently to Monica Kraft, MD, an internationally renowned physician-scientist who specializes in translational asthma research at the University of Arizona (UA) College of Medicine – Tucson and the UA Health Sciences’ Asthma and Airways Diseases Research Center, will seek a better understanding of mediators that help control lung inflammation and improved therapies to reduce severe attacks in those with asthma.
Funded through the National Institute of Allergy and Infectious Diseases (NIAID), the grant will support a research study, “Dysfunction of Innate Immunity in Asthma,” with three projects, including analysis of human samples of people with asthma and investigation of genetic markers related to dysfunctional immune response mechanisms in asthma. The goal is to develop a better understanding of those mechanisms and refine novel therapies to moderate or eliminate asthma attacks and enable asthma sufferers to breathe easier.
Analysis will focus on dysfunctional single nucleotide polymorphisms (SNPs or “snips”) of surfactant protein A (SP-A), a lipid constituent of surfactant known as POPG (palmitoyl-oleoyl-phosphatidylglycerol) and Toll-like receptor interacting protein (Tollip). Surfactant helps to open up aveolar sacs in the lungs and change surface tension so lungs can expand. SP-A, POPG and Tollip act as mediators, signaling synergistically which foreign irritants or conditions in the lungs to attack or not. Each perform critical negative regulatory functions interacting cooperatively to offer protection from allergic inflammation and viral exacerbations of asthma—but, when impaired, cause more acute reactions in asthma sufferers.
“We’ll look at how certain airway cells handle infectious agents in the setting of allergic inflammation in asthma,” Dr. Kraft said. “We’ve found, in humans, not all SP-A is created equal. The same holds true for Tollip. Depending on the genetics of your SP-A or Tollip, their function can be impaired. So, if you have these impaired or dysfunctional aspects of host defense and suffer from asthma, the combination can be very detrimental—leading to more allergic inflammation and asthma attacks.”
“UAHS has some of the best minds in the world working to treat and cure asthma, and this grant from NIH further strengthens the research under way at the UAHS Asthma and Airway Diseases Research Center,” said UA President Ann Weaver Hart. “We are incredibly proud of this work and the good outcomes it will help create for patients.”
“This research also dovetails well into the mission of the recently funded NIH Precision Medicine Initiative Cohort Program, which includes UAHS, to improve prevention and treatment of disease based on individual needs and diverse populations,” said Joe G.N. “Skip” Garcia, MD, UA senior vice president for health sciences, the Dr. Merlin K. DuVal Professor of Medicine and an elected member of the National Academy of Medicine.
The study is part of NIAID’s U19 Cooperative Research Program, which involves about a dozen Asthma and Allergic Diseases Cooperative Research Centers across the country—of which the UA is the newest.
This research is supported by the NIH under award number 1 U19AI125357-01.