PITTSBURGH – For many people with asthma, air-quality advisories are harbingers of worsening symptoms. But for reasons science has struggled to explain, the extent to which pollution exacerbates asthma varies widely from person to person.
In a study published today in eBioMedicine, researchers from the University of Pittsburgh School of Public Health, in collaboration with the Severe Asthma Research Program (SARP), identified biological pathways that begin to uncover this mystery, showing how air-pollution exposure interacts with a person’s genes. The study—which is among the largest and most comprehensive of its kind to date—could eventually lead to new avenues for asthma-drug development, as well as potential new biomarkers and public-health interventions targeted to those who are most vulnerable to pollution-exacerbated asthma.
Using data from nearly 1,000 adults with asthma across the country who had enrolled in SARP, the analysis included a combination of whole genome sequencing, air pollution exposure data and gene-expression profiling. Among the thousands of genes in the human genome, the team focused on about 450 genes that control oxidative stress, a process in which highly reactive molecules can damage cells and tissues.
“Those stresses on cells can translate into serious physiologic effects, like worsening lung function or asthma exacerbations,” said Sally Wenzel, M.D., corresponding author, chair of Pitt Public Health’s Department of Environmental and Occupational Health and director of Pitt’s Asthma and Environmental Lung Health Institute at UPMC, who co-led the study with Shuangjia Xue, a recent graduate of the department’s Ph.D. program.
The team focused on how these genes interacted with the environmental stress of exposure to fine particulate matter known as PM2.5. These microscopic particles, with a diameter less than that of a human hair (less than 2.5 microns), are small enough to penetrate deep into the lungs and are widely considered one of the most harmful components of air pollution.
A clear relationship emerged.
“In these individuals who were living with asthma, the higher their exposure to this particulate matter, the lower their lung function overall,” said Wenzel, adding that the study focused on people who were already living with asthma, rather than in the process of developing the disease.
The study was the first of its kind to use human airway samples in an analysis of gene transcription—that is, how DNA is converted into RNA, which in turn directs cells to produce proteins. “Genes lay out who we could be, but the RNA, and the proteins they transcribe, are what make us who we are,” Wenzel said. The airway epithelial cell samples were collected through bronchial brushings in a subset of about 200 study participants. The data showed how gene activity changed in response to pollution exposure.
The researchers found that the most vulnerable patients carried variants in seven oxidative stress–related genes that shape how the body responds to cellular damage from pollution. These genetic variants appear to influence how airway cells respond to the PM2.5 exposure, with some variants enhancing protection from PM2.5, while others appear to worsen the damage.
Individuals with less common variants in two specific genes, called OXSR1 and PXDN, had disproportionately worse lung function due to lower protective RNA responses to pollution. Those with a specific variant in another gene, called TPO, had worse lung function, as well, but for them, it was due to stronger RNA responses.
The molecular pathways described in the study could point to targets for new therapies—and open the door to much more.
“You could imagine a simple test for a panel of genes that could be used to flag someone as highly susceptible to the effects of pollution,” said Wenzel. That kind of approach could enable both precision medicine—tailoring care to an individual—and precision public health—targeting interventions to specific populations most likely to benefit.
The team’s next steps include digging deeper into the pathways identified in this study and testing whether targeted interventions, ranging from behavioral changes to targeted anti-oxidant therapies, can blunt the harmful effects of pollution in high-risk individuals.
“We’re already exploring some of these pathways,” Wenzel said. “Ultimately, while reducing the amount of pollution remains the most effective approach, the findings from our study suggest we could develop interventions specific to at-risk people that would lessen the impact of pollution.”
Other authors on the study were Shuangjia Xue, Ph.D., Seyed Mehdi Nouraie, M.D., Ph.D., and Jiebiao Wang, Ph.D., all of Pitt; Xingnan Li, Ph.D., of Icahn School of Medicine at Mount Sinai; Deborah Meyers, Ph.D., and Eugene R Bleecker, M.D., both of University of Arizona; Victor E. Ortega, M.D., Ph.D., of Mayo Clinic; Mario Castro, M.D., MPH, of University of Kansas Medical Center; Loren C. Denlinger, M.D., Ph.D., and Nizar Jarjour, M.D., both of University of Wisconsin–Madison; Serpil Erzurum, M.D., of Cleveland Clinic; Elliot Israel, M.D., of Harvard University and Brigham and Women's Hospital; Prescott Woodruff, M.D., Ph.D., Stephanie Christenson, M.D., and John Fahy, M.D., all of University of California San Francisco; Wendy C Moore, M.D., of Wake Forest School of Medicine; Kaharu Sumino, M.D., Ph.D., of Washington University; and Bruce Levy, M.D., of Brigham and Women's Hospital.
This research was supported by the National Institutes of Health (HL145406, U01 HL146002, U10 HL109152, U10 HL109168, U10 HL109172, U10, HL109164, U10 HL109086, U10 HL109257, U10 HL109146 and U10 HL109250).
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About the University of Pittsburgh School of Public Health
Founded in 1948, the University of Pittsburgh School of Public Health is a top-ranked institution of seven academic departments partnering with stakeholders locally and globally to create, implement and disseminate innovative public health research and practice. With hands-on and high-tech instruction, Pitt Public Health trains a diverse community of students to become public health leaders who counter persistent population health problems and inequities.
Journal
EBioMedicine
Method of Research
Randomized controlled/clinical trial
Subject of Research
Human tissue samples
Article Title
A cross-sectional study of oxidative stress pathway genotypes and their interactions with environmental pollutant levels identifies associations with gene expression and lung function
Article Publication Date
23-Jun-2026
COI Statement
Shuangjia Xue, Seyed Mehdi Nouraie, Jiebiao Wang, and Xingnan Li, Deborah Meyers, and Serpil Erzurum declare no conflicts of interest. The following authors declared conflicts the following conflicts unrelated to the current manuscript. Eugene R. Bleecker received grants/ contracts from AstraZeneca, Sanofi Genzyme, and TEVA (paid to institution) and NIH NHLBI (SPIROMICS, SARP, EPIPHANY R01, PrecISE; paid to institution); and consulting fees from AstraZeneca. Victor E. Ortega received grants/contracts from NHLBI; participated on independent data monitoring boards for Regeneron and Sanofi and an advisory board for AstraZeneca; and serves as associate editor for JAMA, UpToDate chapter author (asthma genetics), and author for Merck (asthma ). Mario Castro received grants/contracts from the American Lung Association, AstraZeneca, Gala Therapeutics, Genentech, GSK, NIH, Nocion, Novartis, PCORI, Pulmatrix, Sanofi- Aventis, and Regeneron; consulting fees from Allakos, Amgen, Apogee, Apreo Health, Arrowhead Pharmaceuticals, AstraZeneca, Blueprint Medicines, Connect BioPharma, Enveda, Evommune, Generate Biomedicines, GSK, Jasper Therapeutics, Kinaset, Kymera, Novartis, Om Pharma, Pfizer, Pioneering Medicines, Polarean, Regeneron, Sanofi-Aventis, Syneos, Teva, Third Rock Ventures, Uniquity Bio, Upstream Bio, and Verona Pharmaceuticals; payment/honoraria from Amgen, AstraZeneca, MedLearningGroup, Regeneron, and Sanofi-Aventis; and stock in Aer Therapeutics (less than $5 USD value). Loren C. Denlinger received grants/contracts from NHLBI (PrecISE, GRAIL trials), ALA-ACRC (Lung Health Cohort), and PCORI (iCARE trial); study drug support for the PrecISE trial from GlaxoSmithKline, Laurel, Sun Pharma, Vifor/OM Pharma, Vitaeris/CSL Behring, and Vitaflo; consulting fees from OM Pharma; and honoraria from AstraZeneca; additionally, AstraZeneca, Boehringer-Ingelheim, Genentech, GlaxoSmithKline, Sanofi–Genzyme–Regeneron, and TEVA provided financial support for SARP study activities beyond year three of patient follow-up (these companies had no role in study design or data analysis). Elliot Israel received grants/contracts from AstraZeneca, NIH, PCORI, Sanofi, and TEVA (all paid to institution); royalties from UpToDate (Wolters Kluwer); consulting fees from Amgen, AnaptysBio, Apogee Therapeutics, Arrowhead Pharmaceuticals, AstraZeneca, Bain Capital, Chiesi, Clearview Health Partners, Danker and Associates, Ecor1, ERS, Generate Biomedicine, GlaxoSmithKline, Guidepoint, Jasper Therapeutics, Leerink Partners, Merck, Mountainfield, OrbiMed, Reach Market Research, Regeneron, Sanofi, TEVA, The Lancet, Third Rock Ventures, Windrose Consulting Group, and Yuhan (all paid to him); honoraria from AAN, AFI, AstraZeneca, and Regeneron; payment for expert testimony from Cambridge Medical Experts; travel support from AstraZeneca, Sanofi, and NYU Asthma Airways Symposium; advisory board fees from Amgen, AnaptysBio, Apogee Therapeutics, AstraZeneca, Chiesi, and Sanofi; receipt of equipment, drugs, and materials from Circassia, Genentech, TEVA, Sun Pharma, Laurel Pharmaceuticals, Om Pharma, CSL Behring, Amgen, GlaxoSmithKline, and Sanofi-Regeneron (for various NIH-funded studies); and stock options in Vorso (unpaid). Prescott Woodruff received grant support from NIH (SARP); consulting fees from AnaptysBio, AbbVie, and Roche; and honoraria for visiting professorships from BWH, Pitt, and UNC. Wendy C. Moore received grant support from NHLBI (SARP program; paid to institution) and grants/contracts from NHLBI (SARP, PrecISE), ALA (ALA-ACRC Lung Health Cohort), and AstraZeneca, GlaxoSmithKline, Aerteia, Amgen, and TEVA (multicenter clinical trials; paid to institution); and consulting fees from AstraZeneca (advisory board; personal fees). Stephanie Christenson received grants/contracts from NIH, the American Lung Association, COPD Foundation, Department of Defence, and Uniquity Bio (all paid to institution); consulting fees from Sanofi, AstraZeneca, AbbVie, Apogee Therapeutics, and Genentech (all paid to her); honoraria for lectures and presentations from Sanofi, Regeneron, Horizon CME, AstraZeneca, MJH Holdings, WebMD, UpToDate, HCPLive, Answers in CME, PeerView CME, and ReachMD (all paid to her); travel support from Sanofi/ Regeneron and GlaxoSmithKline; advisory board fees from Sanofi, AstraZeneca, Regeneron, Illuminate Health, Verona Pharma, Amgen, Uniquity Bio/Devpro Pharma, Kymera Therapeutics, GSK, Genentech, and Gilead (all paid to her); and an unpaid leadership role with the American Thoracic Society. John Fahy received grants/contracts from NIH/NHLBI; consulting fees from Suzhou Connect Biopharmaceuticals, Ltd. and Aer Therapeutics; patents PCT/US2014/ 028656 and PCT/US19/50475 (thiol-modified saccharides as drugs to treat mucus-associated lung disease); and stock options from Suzhou Connect Biopharmaceuticals, Ltd. and a stock grant from Aer Therapeutics. Nizar Jarjour received consulting fees from GSK, Chiesi, AstraZeneca, and General Medicines. Bruce Levy received grant support from NHLBI, AstraZeneca, Amgen, Genentech, GlaxoSmithKline, Novartis, Sanofi-Genzyme-Regeneron, and TEVA (all paid to institution for SARP) and SRA (paid to institution); royalties from Propeller Health; and stock options from Nocion Therapeutics. Sally E. Wenzel received grant support from NIH/NIAID/NHLBI (paid to institution) and Regeneron (investigator-initiated study); consulting fees from Regeneron, Chiesi, and Eli Lilly (paid to her); and stock in Aer Therapeutics (paid to her and her spouse). Kaharu Sumino received honoraria for a lecture from Kyorin pharmaceutical, support for attending Japan Respiratory Society meeting 2024, participates on the Data Safety and Monitoring Board at The University of Chicago Illinois for ALOHA trial funded by NIH, and is a member of the guideline panel for Joint Task force for American Academy of Allergy, Asthma & Immunology and American College of Allergy, Asthma and Immunology, Guideline for Management of difficult-to-control and severe asthma . Serpil Erzurum has a leadership or fiduciary role in Cleveland Clinic.