Virus co-opts immune protein to avoid antiviral defences

Viruses have many strategies to avoid immune system defenses. They often do this by hijacking the immune system's own proteins. One immune protein that is frequently targeted by viruses, including HIV, hepatitis C, and the SARS coronavirus, is called cyclophilin A (CypA). Understanding how CypA is used by viruses could help scientists develop drugs that work against all of them, including the SARS-CoV-2 virus causing the COVID-19 pandemic.

"Previously, clinical trials have shown that blocking CypA reduces the ability of the hepatitis C virus to replicate and boosts the immune response," explains lead author Che Colpitts, Assistant Professor of Biomedical and Molecular Sciences at Queen's University, Kingston, Canada. "We set out to understand how CypA helps hepatitis C evade the immune system."

In the experiments, the team used hepatitis C-infected human liver cancer cells with and without a functioning innate immune system. The innate immune system scans the body for potential threats such as viruses or bacteria and triggers a response. The scientists used a tool called a short hairpin RNA to selectively silence CypA and found that this stopped the virus from replicating only in the liver cells with a functioning innate immune system. They also showed that drugs called cyclophilin inhibitors help block the virus from co-opting CypA and prevent it from multiplying.

CypA is known to attach to an immune protein called protein kinase R (PKR), affecting its ability to detect viruses. So, the team used a gene-editing tool called CRISPR/Cas9 to cut out the gene for PKR in human liver cells with a working innate immune system. In cells without PKR, the cyclophilin inhibitors were less able to stop the virus from reproducing. This happened because PKR was not there to identify the virus and trigger antiviral defenses.

"These findings reveal a new antiviral defence mechanism that suppresses virus growth," says senior author Greg Towers, Professor of Molecular Virology at University College London, UK. "This opens the door for the development of CypA-targeting antiviral drugs that can be used against many currently untreatable viruses."