Steroids may do more harm than good in some cases of severe asthma
PITTSBURGH, July 6, 2017 – Researchers from the University of Pittsburgh Schools of the Health Sciences and UPMC have uncovered the molecular mechanism underlying corticosteroid resistance in severe asthma. The new findings have important clinical implications, suggesting that corticosteroids, the main treatment for asthma, may worsen the disease in this group of patients.
The research was published today in the journal JCI Insight.
Asthma is a lifelong disorder characterized by airway inflammation that leads to wheezing, breathlessness and coughing. It affects up to 10 percent of the population of the developed world, including more than 20 million Americans. Inhaled corticosteroids can reduce airway inflammation, but these drugs are ineffective in 5 to 10 percent of patients with severe asthma.
"The current therapies are inadequate for a subset of patients with a severe form of asthma," said the study's co-senior author Anuradha Ray, Ph.D., professor of immunology and medicine and Endowed Chair in Lung Immunology at Pitt's School of Medicine. "We need to better understand their underlying disease and why they are poorly responsive to corticosteroids in order to identify novel targets for future therapies."
The researchers had previously shown that increased levels of the inflammatory protein interferon-gamma are produced in the airways of about half of severe asthma patients. Using a mouse model of severe asthma, the researchers also showed that interferon-gamma was responsible for poor lung function.
In the new study, they investigated whether interferon-gamma signaling is responsible for the poor response to corticosteroid therapy of some severe asthmatics. The work focused on CXCL10, an inflammatory protein that is induced by interferon-gamma and recruits the immune cells that produce it, perpetuating the cycle of inflammation.
CXCL10 was elevated in the lung cells of about half of severe asthma patients treated with a high dose of corticosteroids. In addition, CXCL10 levels were higher in severe asthmatics than in patients with milder asthma whose symptoms were managed well by corticosteroids or other treatment modalities.
When the researchers broke all asthma patients down into two groups–high and low CXCL10–they found that the high CXCL10 group had worse asthma control, as evidenced by more emergency department visits and asthma flares in the past year.
Next, the team used cultured immune cells to show that corticosteroids, which have broad anti-inflammatory and immunosuppressive functions, fail to suppress CXCL10 gene expression in immune cells. They found that this occurs because of a surprising mechanism–corticosteroids actually stabilize the signal from interferon-gamma that stimulates CXCL10 production.
"Our findings show that CXCL10 is elevated in some patients with severe asthma and that corticosteroids have little impact on its production," said co-senior author Sally Wenzel, M.D., professor of medicine in Pitt's School of Medicine and director of the University of Pittsburgh Asthma Institute at UPMC. "While corticosteroids are the mainstay asthma treatment, our findings suggest that these medications are of limited help to patients with high levels of interferon-gamma and CXCL10, and may even be harmful over time."
The team plans to further investigate this pathway in search of ways to block the inflammatory loop perpetuated by CXCL10 and interferon-gamma.
"Over the next few years, we also hope to show that CXCL10 can be used as a biomarker in the clinic to help identify patients who will not respond to corticosteroids, sparing them from the significant side effects of these medications," Ray said.
Additional authors on the study are Marc Gauthier, M.D., Krishnendu Chakraborty, Ph.D., Timothy Oriss, Ph.D., Mahesh Raundhal, Ph.D., Sudipta Das, Ph.D., Jie Chen, M.E., Rachael Huff, B.A., Ayan Sinha, Merritt Fajt, M.D., and Prabir Ray, Ph.D., all of Pitt.
Funding was provided by National Institutes of Health grants AI106684, HL113956, AI048927, AI100012, HL114453, HL122307 and HL69174.
About the University of Pittsburgh Schools of the Health Sciences
The University of Pittsburgh Schools of the Health Sciences include the schools of Medicine, Nursing, Dental Medicine, Pharmacy, Health and Rehabilitation Sciences and the Graduate School of Public Health. The schools serve as the academic partner to the UPMC (University of Pittsburgh Medical Center). Together, their combined mission is to train tomorrow's health care specialists and biomedical scientists, engage in groundbreaking research that will advance understanding of the causes and treatments of disease and participate in the delivery of outstanding patient care. Since 1998, Pitt and its affiliated university faculty have ranked among the top 10 educational institutions in grant support from the National Institutes of Health. For additional information about the Schools of the Health Sciences, please visit http://www.health.pitt.edu.
A $14 billion world-renowned health care provider and insurer, Pittsburgh-based UPMC is inventing new models of patient-centered, cost-effective, accountable care. UPMC provides nearly $900 million a year in benefits to its communities, including more care to the region's most vulnerable citizens than any other health care institution. The largest nongovernmental employer in Pennsylvania, UPMC integrates 65,000 employees, more than 25 hospitals, 600 doctors' offices and outpatient sites, and a more than 3.2 million-member Insurance Services Division, the largest medical and behavioral health services insurer in western Pennsylvania. Affiliated with the University of Pittsburgh Schools of the Health Sciences, UPMC ranks No. 12 in the prestigious U.S. News & World Report annual Honor Roll of America's Best Hospitals. UPMC Enterprises functions as the innovation and commercialization arm of UPMC while UPMC International provides hands-on health care and management services with partners in 12 countries on four continents. For more information, go to UPMC.com