Fat-storing cell structures may block viral spread by recruiting antiviral proteins
La Trobe University scientists have uncovered the critical role fatty cell structures play in our body's early detection and defense against viruses. Published in Nature Communications, the discovery could open the door to a new type of antiviral strategy that harnesses the body's innate defense mechanisms rather than targeting individual viruses.
The study revealed the fatty structures—called "lipid droplets"—stop viruses from spreading by changing their structure to include specific fatty acids while signaling to the immune system to send key antiviral proteins.
By including two of these fatty acids in artificial lipid droplets, researchers were able to reduce viral replication and boost antiviral immune signals.
From fat stores to defenders
Lead researcher Professor Karla Helbig said lipid droplets were until now believed to be passive fat stores.
"This research shows they are vital, active control centers to defend us against viruses," Professor Helbig said.
"Instead of targeting viruses themselves—which often leads to drug resistance—this research points to ways of enhancing the body's own antiviral machinery.
"By manipulating lipid droplets or delivering specific antiviral fats, it may be possible to develop broad-spectrum antivirals that work against many different types of viruses."
A broader pandemic tool
Co-lead researcher Dr. Ebony Monson said the discovery could help scientists prepare for the next pandemic.
"The COVID-19 pandemic caused millions of deaths worldwide and trillions of dollars in economic damage," Monson said.
"We largely rely on vaccines, but these take time to develop, only defend us against specific viruses and, as viruses mutate quickly, they can easily evade the protection vaccines provide.
"This study could lead to the development of a new wave of antiviral drugs that target a common pathway instead of specific viruses, helping to boost immune response and lower disease burden.
"We hope our research will contribute to faster, more resilient responses to emerging viral threats and significantly improve global pandemic preparedness."
This research was conducted in collaboration with scientists from the University of Sydney, RMIT and the University of Melbourne's Bio21 Institute.
Publication details
Ebony A. Monson et al, Integrative proteomics and lipidomics reveals dual roles for lipid droplets in the host cell antiviral response, Nature Communications (2026). DOI: 10.1038/s41467-026-74016-w
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Citation: Fat-storing cell structures may block viral spread by recruiting antiviral proteins (2026, July 24) retrieved 24 July 2026 from https://phys.org/news/2026-07-fat-cell-block-viral-antiviral.html
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