New research NETs a fresh angle for treating severe inflammation

As we’ve seen during the COVID-19 pandemic, serious infections sometimes trigger an excessive inflammatory reaction that does as much harm — or more — than the infection itself. New research at Boston Children’s Hospital and Brigham and Women’s Hospital suggests a potential way to block this hyperinflammation response by repurposing or modifying an existing drug.

The findings could potentially lead to a new treatment not just in COVID-19, but also for other life-threatening inflammatory conditions like sepsis and acute respiratory distress syndrome (ARDS) that currently have no specific treatment.

NETs, COVID-19, and inflammation

COVID-19, sepsis, and ARDS have something in common: All of them involve neutrophil extracellular traps, or NETs.

So what are NETs? They’re webs of DNA and toxic proteins that neutrophils, first-responder cells in the immune system, spew out to entrap bacteria or viruses, in a last-ditch attempt to contain the infection. (The neutrophils themselves, having lost their DNA, die in the process.)

“NETs are the final step,” says Ivan Zanoni, PhD, an immunology researcher at Boston Children’s and co-senior investigator on the study with Jeffrey Karp, PhD, of Brigham and Women’s. “If NETs appear, it suggests that other means of fighting the infection have failed. Neutrophils get the signal, ‘Give it everything you have.’”

But there’s a cost to making NETs. A growing body of research shows that the formation of too many NETs can lead to dangerous levels of inflammation, to blood clots such as those found in sepsis and severe COVID-19, and to direct tissue damage like that seen in severe lung infections and ARDS.

Preventing NETs from forming

The new study, led by Zanoni, Karp, and first author Valentina Poli, PhD, of Boston Children’s, suggests a way of curbing NETs and blocking potentially fatal inflammatory reactions. In the journal iScience this month, the researchers show that a drug called ricolinostat interferes with an early step involved in NET formation in neutrophils from both mice and humans and in three mouse models.

To form NETs, neutrophils first have to release their own DNA. This requires a specific group of enzymes called histone deacetylases (HDACs), which help open up the packaging around the DNA, known as chromatin. Ricolinostat, an HDAC inhibitor, blocks two classes of HDACs, class I and IIb.

“If you inhibit HDACs, you cannot open chromatin,” says Zanoni.

If chromatin can’t open, the neutrophil cannot release its DNA and NETs cannot form. In the three mouse models — viral pneumonia, bacterial pneumonia, and a model of septic shock — the drug decreased NET formation and dampened inflammation. It protected lung function in the pneumonia models and reduced the harm caused by septic shock, appearing to reduce blood clot formation.

Working toward a clinical trial

Ricolinostat is currently in clinical trials for several cancers and for peripheral neuropathy in diabetes. Since it’s already gone through preclinical testing, Zanoni and Karp are looking to get it into clinical trials for severe inflammatory conditions. Zanoni’s lab has one modified version of ricolinostat that is also looking promising for blocking NET formation.

“Our work has potential to immediately help with COVID-19 to dampen the inflammatory response and turn it into something relatively harmless like a mild cold,” says Karp. “Inhibiting NETs represents a new therapeutic strategy for pulmonary diseases, autoimmune diseases like rheumatoid arthritis and systemic lupus erythematosus, diabetes, and cancer,” says Karp.

Zanoni adds a note of caution. “NETs exist because they are protective,” he says. “We have to be careful in blocking biology that is protective, and avoid suppressing the immune system too much.”

The study was supported by the National Institutes of Health, the Lloyd J. Old STAR Program, the Burroughs Wellcome Fund, and the National Cancer Institute. Poli, Karp, Zanoni, and several coauthors have submitted a patent related to the findings of this work.

About Boston Children’s Hospital

Boston Children’s Hospital is ranked the #1 children’s hospital in the nation by U.S. News & World Report and is the primary pediatric teaching affiliate of Harvard Medical School. Home to the world’s largest research enterprise based at a pediatric medical center, its discoveries have benefited both children and adults since 1869. Today, 3,000 researchers and scientific staff, including 10 members of the National Academy of Sciences, 25 members of the National Academy of Medicine and 12 Howard Hughes Medical Investigators comprise Boston Children’s research community. Founded as a 20-bed hospital for children, Boston Children’s is now a 415-bed comprehensive center for pediatric and adolescent health care. For more, visit our Answers blog and follow us on social media @BostonChildrens, @BCH_Innovation, Facebook and YouTube.

About Brigham Health

Brigham Health, a global leader in creating a healthier world, consists of Brigham and Women's Hospital, Brigham and Women’s Faulkner Hospital, the Brigham and Women’s Physicians Organization and many related facilities and programs. With more than 1,000 inpatient beds, approximately 60,000 inpatient stays and 1.7 million outpatient encounters annually, Brigham Health’s 1,200 physicians provide expert care in virtually every medical and surgical specialty to patients locally, regionally and around the world. An international leader in basic, clinical and translational research, Brigham Health has nearly 5,000 scientists, including physician-investigators, renowned biomedical researchers and faculty supported by over $700 million in funding. The Brigham’s medical preeminence dates back to 1832, and now, with 19,000 employees, that rich history is the foundation for its commitment to research, innovation, and community. Boston-based Brigham and Women’s Hospital is a teaching affiliate of Harvard Medical School and dedicated to educating and training the next generation of health care professionals. For more information, resources, and to follow us on social media, please visit brighamandwomens.org.

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