News Release

Researchers identify protein that could reduce death, improve symptoms in flu and other infections

New research identifies potential protective agent against flu

Peer-Reviewed Publication

University of Maryland School of Medicine

A new study by researchers at the University of Maryland School of Medicine has identified an innovative strategy for treating influenza, and perhaps other infectious diseases as well. Scientists showed that a small protein called retrocyclin-101 (RC-101) could potentially improve the symptoms and mortality associated with the flu and possibly other types of infectious illness as well.

The protein is unique in that it not only targets the flu virus itself, but also the harmful inflammation the virus triggers in the host.

While the effect of RC-101 has been studied as a flu treatment in cells before, it has never been studied in animals. The research appears in the most recent issue of the Journal of Leukocyte Biology.

"Every year, thousands of people across the country die from the flu or its complications -- despite widespread use of annual influenza vaccines," said the study's lead author, Daniel J. Prantner, a research associate in the Department of Microbiology and Immunology at the University of Maryland School of Medicine (UM SOM). "We think that this protein could lead to medicines that could be a powerful tool in the battle against this disease, and against inflammation in general."

For this study, Dr. Prantner and his colleagues studied the effects of RC-101 on human cells, and in an animal model of flu, using mice. The researchers studied human immune cells, and found that RC-101 had two positive effects. First, it blocked the flu virus from infecting the cells; second it blocked the runway inflammation that is behind most symptoms of influenza infection, such as fever, pain, lethargy, and trouble breathing. This double action is unique, Dr. Prantner says.

In the animal model, the researchers infected two groups of mice with a dose of influenza that is typically lethal. They gave one of these groups RC-101 two days after infection for a total of five days, and gave the other group a placebo. The mice that were treated with RC-101 exhibited less severe symptoms of the flu and also decreased rates of death. Among the control group, 90 percent of the mice died; among the group that was given RC-101, only 20 percent died.

Although RC-101 does not exist in humans, it does exist in some other animals, including orangutans, and provides powerful antiviral protection. It appears to have been lost over the course of recent primate evolution. Chimpanzees and gorillas, for example, do not have it.

One of the study's principal investigators, Alfredo Garzino-Demo, PhD, an associate professor in the UM SOM Department of Microbiology and Immunology and at the UM SOM Institute of Human Virology, is planning research to see whether the protein can be effective against Dengue, Zika, and other viral infections that can cause damage via inflammation.

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Other authors on the paper include the other principal investigator, Stefanie Vogel, PhD, a professor in the UM SOM Department of Microbiology and Immunology; Kari Ann Shirey, PhD, assistant professor in the UM SOM Department of Microbiology and Immunology; Wendy Lai, Laboratory Research Supervisor in the in the UM SOM Department of Microbiology and Immunology; Wuyuan Lu, PhD, professor in the UM SOM Department of Biochemistry and Molecular Biology, and Co-Director Of the Division Of Basic Science; and Alexander M. Cole, PhD, a professor in the Burnett School of Biomedical Sciences at the University of Central Florida College of Medicine.


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