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The research, published in the journal Science Translational Medicine, demonstrates the potential of the vaccine to work through the mucosal tissue to neutralize SARS-CoV-2, limiting infections and the spread of active viruses in airborne particles.
”Considering most of the world is under-immunized — and this is especially true of children — the possibility that a vaccinated person with a breakthrough infection can spread COVID to unimmunized family or community members poses a public health risk,” said Stephanie N Langel from Duke University Medical Center in the US.
”There would be a substantial benefit to developing vaccines that not only protect against disease but also reduce transmission to unvaccinated people,” Langel said in a statement.
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The spike protein is used by SARS-CoV-2 to enter and infect the human cells.
The human vaccine is designed to be taken as a pill, they said.
In studies using hamsters, the vaccine elicited a robust antibody response in blood and the lungs.
When the animals were exposed to the SARS-CoV-2 virus at high levels, prompting breakthrough infections, they were less symptomatic than non-vaccinated hamsters and had lower amounts of infectious virus in the nose and lungs.
Because of this, they did not shed as much virus through normal airborne exposures, according to the researchers.
Unlike vaccines that are injected into the muscle, they said, mucosal immunizations increase the production of immunoglobulin A (IgA) — the immune system’s first line of defense against pathogens — in the nose and lungs.
These mucosal ports of entry are then protected, making it less likely that those who are vaccinated will transmit the infectious virus during a sneeze or cough, the researchers said.
”Our data demonstrate that mucosal immunization is a viable strategy to decrease the spread of COVID through airborne transmission,” Langel said.
The researchers noted that the study focused on the original SARS-CoV-2 virus, and new studies will be designed to test the vaccine against Omicron variants.