DNA of peanut-allergic kids changes with immune therapy, study finds
Research led by immunologist Kari Nadeau shows a blood test could determine whether patients who have been desensitized to their peanut allergies need to continue eating peanuts daily to retain their tolerance.
Treating a peanut allergy with oral immunotherapy changes the DNA of the patient’s immune cells, according to a new study from the Stanford University School of Medicine and Lucile Packard Children’s Hospital Stanford. The DNA change could serve as the basis for a simple blood test to monitor the long-term effectiveness of the allergy therapy.
Peanut allergy, like other food allergies, currently has no cure. Scientists are conducting clinical trials of doctor-supervised immunotherapy, in which peanut-allergic patients take increasing amounts of peanut powder to try to desensitize them to the peanut allergen. At the end of the trial, patients are usually asked to eat some peanuts every day for the rest of their lives.
“At first, eating two peanut butter cups a day might seem fun, but it gets a little boring and a lot of people might stop,” said Kari Nadeau, MD, PhD, associate professor of pediatrics at Stanford and an immunologist at Stanford Hospital & Clinics and Lucile Packard Children’s Hospital Stanford. Until now, doctors could not test whether patients who had completed immunotherapy could safely stop eating daily doses of peanuts, she said. “Our new finding can help us try to determine whether, for the long term, someone’s allergy has truly been shut off so people can eat ad lib.”
Nadeau is the senior author of a paper describing the new findings, published online Jan. 31 in the Journal of Allergy and Clinical Immunology.
In the new study, Nadeau’s team examined 20 peanut-allergic children and adults who had completed two years of immunotherapy, which enabled them to eat one 4-gram serving of peanuts daily without experiencing a major allergic reaction.
The patients were asked to stop eating peanuts for three months and then were given a small amount of peanut powder to see if their allergy returned. Thirteen of the patients regained their allergy, while seven did not. The researchers compared the immune cells in the blood of patients from the two groups. Blood samples from peanut-allergic patients who had never received oral immunotherapy were used as a control.
The researchers focused on the regulatory T cells, which are white blood cells that help to suppress an allergy response. In these cells, the DNA at a gene called forkhead box protein 3, or FOXP3, was slightly different in each of the three groups of patients. The FOXP3 gene has previously been shown to play a role in allergies.
The researchers did not detect changes in the genetic code itself. Rather, there were different numbers of methyl groups attached to the DNA. These molecular add-ons to the DNA control the rate at which the gene is expressed, turning the volume up or down on the gene’s voice in the cell. Patients who maintained their tolerance to peanuts had low levels of DNA methylation at FOXP3, while those who regained their allergy had an intermediate level. Peanut-allergic patients who had not received oral immunotherapy (the control group) had a high level of DNA methylation at the FOXP3 gene.
The DNA change could possibly be used to monitor the effectiveness of oral immunotherapy, Nadeau said, but needs further testing. The blood test necessary to monitor the DNA is inexpensive, requires only a small amount of blood and uses common lab equipment. However, Food and Drug Administration approval would be needed before the test could be used clinically for this purpose.
“It’s interesting that the change we saw is at the epigenetic level,” Nadeau said, referring to changes in gene activity and expression caused by factors other than DNA sequence. “This might help us tell people if they can safely go off of immunotherapy, or if they need to continue to eat the food every day.” The test could also help researchers determine whether some individuals would benefit from longer courses of immunotherapy, she added.
Future studies are needed to determine whether the genetic change to FOXP3 is passed on to the children of people who have completed oral immunotherapy.
Other Stanford co-authors of the paper were research assistants Aleena Syed, Marco Garcia, Robert Bucayu and Arunima Kohli; laboratory manager Shu-Chen Lyu; Satoru Ishida, PhD, visiting scholar; Mindy Tsai, DMSc, senior resident scientist in pathology; Holden Maecker, PhD, associate professor of microbiology and immunology; Gerri O’Riordan, RN, chief operating officer and senior director of regulatory compliance for the Stanford Alliance for Food Allergy Research; and Stephen Galli, MD, professor of microbiology and immunology.
The research was funded by Food Allergy Research & Education, the Fund for Food Allergy Research at Stanford, the National Institute of Allergy and Infectious Diseases (grant R211R21AI09583801) and the Children’s Health Research Institute/Lucile Packard Foundation for Children’s Health. The research also was supported by the National Center for Research Resources (grant UL1RR024128) and the National Center for Advancing Translational Science (grant UL1TR000093).
Information about Stanford’s Department of Pediatrics, which also supported this research, is available at http://pediatrics.stanford.edu.
Stanford Medicine integrates research, medical education and health care at its three institutions - Stanford University School of Medicine, Stanford Health Care (formerly Stanford Hospital & Clinics), and Lucile Packard Children's Hospital Stanford. For more information, please visit the Office of Communication & Public Affairs site at http://mednews.stanford.edu.