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Promising Gene-Based Approaches to Repair Lethal Lung Injury in the Elderly from COVID-19, Pneumonia, Flu, Sepsis

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09/20/2023
eurekalert.org

Discovery from the lab of Youyang Zhao, PhD, from Stanley Manne Children’s Research Institute at Ann & Robert H. Lurie Children’s Hospital of Chicago offers promising treatment approaches for acute respiratory distress syndrome (ARDS) in the elderly that can be caused by severe COVID-19, pneumonia, flu or sepsis. Currently there are no pharmacological or cell-based treatments for ARDS.

Dr. Zhao’s research established that a gene called FOXM1 is important in the repair of blood vessel through regeneration of endothelial cells, which line the vessels of the lung. He found that aging impairs this gene’s expression, which may be responsible for the high fatality rate from ARDS in people over 75 years of age – 10 times higher compared to young adults.

Working with a mouse model, Dr. Zhao also demonstrated that FOXM1 expression could be reactivated by two methods, which restore the gene’s function and improve survival from ARDS in the aged mice. As seen in aged mice, FOXM1 expression was inhibited in elderly COVID-19 patients. His findings were published in the journal Science Translational Medicine.

One approach involved a low dose of a repurposed FDA-approved cancer drug, decitabine, which was successful at reactivating FOXM1 expression, and so promoting vascular repair and regeneration. This drug currently is in a clinical trial for treating severe COVID-19. Dr. Zhao’s findings suggest that a lower and safer dose could be used, and that the treatment should be targeted to older patients, since the gene’s activity remains intact in younger people.

“We found that decitabine improved vascular repair, inflammation resolution and survival in aged mice, but the drug had no effects on vascular repair in young adult mice,” said Dr. Zhao, Director of the Program for Lung and Vascular Biology and Head of Section for Injury Repair and Regeneration Research at Manne Research Institute at Lurie Children’s, as well as Professor of Pediatrics, Medicine and Pharmacology at Northwestern University Feinberg School of Medicine. “It would be important to focus decitabine treatment on the elderly population, in which FOXM1 expression needs to be activated to promote recovery and reduce mortality. The next step is a clinical trial of a lower dose of the drug for ARDS in the elderly.”

Dr. Zhao also demonstrated effectiveness of an alternative approach to reactivate the gene – endothelium-targeted nanoparticle gene delivery – a technology he developed and patented. It is a more precise strategy, which may also be safer than decitabine treatment.

“Because FOXM1is also an oncogene, unwanted induction of FOXM1 in other cell types by decitabine treatment may be a cause for concern,” he explained. “Our nanoparticle gene delivery system delivers FOXM1 only in endothelial cells, where it is needed for lung injury repair and regeneration. This strategy carries great potential for treating any disease caused by endothelial dysfunction including cancer and cancer metastasis. It will need further testing before clinical use.”

Dr. Zhao is the William G Swartchild, Jr. Distinguished Research Professor at Lurie Children’s.

Research at Ann & Robert H. Lurie Children’s Hospital of Chicago is conducted through Stanley Manne Children’s Research Institute. The Manne Research Institute is focused on improving child health, transforming pediatric medicine and ensuring healthier futures through the relentless pursuit of knowledge. Lurie Children’s is a nonprofit organization committed to providing access to exceptional care for every child. It is ranked as one of the nation’s top children’s hospitals by U.S. News & World Report. Lurie Children’s is the pediatric training ground for Northwestern University Feinberg School of Medicine.



Journal

Science Translational Medicine

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.

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Schedule14 Jun 2024