A vaccine for hepatitis C has eluded scientists for more than 30 years, for several reasons. For one, the virus that causes the disease comes in many genetic forms, complicating the creation of a widely effective vaccine. For another, studying hepatitis C has been difficult because options in animals are limited and lab methods using infected cells have not adequately reflected the real-life dynamics of infection.
Now, researchers at Gladstone Institutes have developed a new platform for studying how the human immune system responds to hepatitis C infection. The method, presented in the scientific journal Open Biology, marries microfluidic technology (which allows scientists to precisely manipulate fluid at a microscopic scale) with liver organoids (three-dimensional cell clusters that mimic the biology of real human livers).
“The 3D structure and cellular composition of liver organoids allows us to study viral entry and replication in a highly relevant physiological manner,” says Gladstone Senior Investigator Todd McDevitt, PhD, a senior author of the new study.
“Our approach enables a more controlled and accurate investigation into the immune response to hepatitis C infection,” says Melanie Ott, MD, PhD, director of the Gladstone Institute of Virology and another senior author of the study. “We hope our method will accelerate the discovery of a much-needed vaccine.”












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