A vaccine against rhinoviruses, the predominant cause of the common cold, is achievable, scientists say.
The quest for a vaccine against rhinoviruses may have seemed quixotic, as there are more than 100 varieties circulating around the world. Even so, the immune system can handle the challenge, researchers say.
Vaccines that combine dozens of varieties of rhinovirus at once are effective in stimulating antiviral antibodies in mice and monkeys, researchers report in a new study in the journal Nature Communications. The paper was also posted on BioRxiv before publication.
“We think that creating a vaccine for the common cold can be reduced to technical challenges related to manufacturing,” says Martin Moore, associate professor of pediatrics at Emory University School of Medicine.
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Rhinoviruses are the most common cause of the common cold; other viruses such as respiratory syncytial virus, parainfluenza virus, and adenoviruses can cause them too. Rhinoviruses also exacerbate asthma attacks. Although they come in many varieties, rhinoviruses don’t drift to the same degree that influenza viruses do, Moore says.
Researchers showed in the 1960s that it was possible to vaccinate people against one variety of rhinovirus and prevent them from getting sick when challenged with samples of the same virus. The trouble was the sheer diversity of rhinoviruses—or that’s how it appeared at the time.
“It’s surprising that nobody tried such a simple solution over the last 50 years. We just took 50 types of rhinovirus and mixed them together into our vaccine, and made sure we had enough of each one,” Moore says. “If we make a vaccine with 50 or 100 variants, it’s the same amount of total protein in a single dose of vaccine. The variants are like a bunch of slightly different Christmas ornaments, not really like 50 totally different vaccines mixed.”
A mixture of 25 types of inactivated rhinovirus can stimulate neutralizing antibodies against all 25 in mice, and a mixture of 50 types can do the same thing in rhesus macaques. In this paper, antibodies generated in response to the vaccine were tested for their ability to prevent the virus from infecting human cells in culture. However, the vaccines were not tested for their ability to stop animals from getting sick.
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“There are no good animal models of rhinovirus replication,” Moore says. “The next step would be human challenge models with volunteers, which are feasible because the virus is not very pathogenic.”
Emory has optioned the vaccine technology to a startup company, Meissa Vaccines, Inc., which is pursuing a product development plan with support from the National Institute of Allergy and Infectious Diseases’ vaccine manufacturing services.
Sujin Lee, assistant professor of pediatrics, and research specialist Minh Trang Nguyen are co-first authors of the study, which the National Institute of Allergy and Infectious Diseases and a pilot grant from the Emory/Children’s/Georgia Tech Center for Childhood Infections and Vaccines supported. Experiments with rhesus macaques took place at Yerkes National Primate Research Center.
Moore co-founded and serves as chief scientific officer for Meissa Vaccines, Inc. Lee, Nguyen, and Moore are co-inventors in a patent application describing the rhinovirus vaccine.
Source: Emory University