The New York research team had the idea that modifying antibodies and their subsequent Fc region (the portion of the antibody that connects to immune cells, assisting with immune responses) could potentially lead to more vaccines for different strains of the flu.
Jeffrey Ravetch, senior author of this study, explained that “while the conventional flu vaccine protects only against specific strains, usually three of them, our experiments show that by including modified antibodies within the vaccine it may be possible to elicit broad protection against many strains simultaneously."
For their study, the Rockefeller research team gave clinical participants a vaccine for the H1N1 virus, and viewed the way that antibodies reacted to the virus, and saw that the signaling molecule sialic acid increased in the Fc region of the antibodies. They saw that people with a greater sialylation responded better to the vaccine. They then further studied the Fc region of antibodies through cell cultures and mice and found that Fc regions with high sialylation had a higher affinity for immune responses.
“The new mechanism we have uncovered, by which a vaccine containing sialylated antibodies elicits broadly protective antibodies, could potentially be harnessed to reduce the tremendous morbidity and mortality caused by seasonal influenza virus infections,” said Taia Wang, a clinical instructor at Rockefeller. “We are now looking into applying this strategy toward improving existing vaccines; ideally, this would result in a vaccine that provides life long immunity against flu infections.”
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