Interferon Alpha Subtype-Specific Suppression of HIV-1 Infection In Vivo.
Kerry J LavenderKathrin GibbertKarin E PetersonErik Van DisSandra FrancoisTyson WoodsRonald J MesserAli GawanbachtJanis A MüllerJan MünchKatie PhillipsBrent RaceMichael S HarperKejun GuoEric J LeeMirko TrillingHartmut HengelJacob PiehlerJens VerheyenCara C WilsonMario L SantiagoKim J HasenkrugUlf DittmerPublished in: Journal of virology (2016)
The naturally occurring antiviral protein IFN-α2 is used to treat hepatitis viruses but has proven rather ineffective against HIV in comparison to triple therapy with the antiretroviral (ARV) drugs. Although ARVs suppress the replication of HIV, they fail to completely clear infections. Since IFN-α acts by different mechanism than ARVs and has been shown to reduce HIV proviral loads, clinical trials are under way to test whether IFN-α2 combined with ARVs might eradicate HIV-1 infections. IFN-α is actually a family of 12 distinct proteins, and each IFN-α subtype has different efficacies toward different viruses. Here, we use mice that contain a human immune system, so they can be infected with HIV. With this model, we demonstrate that while IFN-α2 is only weakly effective against HIV, IFN-α14 is extremely potent. This discovery identifies IFN-α14 as a more powerful IFN-α subtype for use in combination therapy trials aimed toward an HIV cure.
Keyphrases
- antiretroviral therapy
- hiv positive
- hiv infected
- human immunodeficiency virus
- hiv testing
- dendritic cells
- hiv aids
- immune response
- hepatitis c virus
- men who have sex with men
- hiv infected patients
- clinical trial
- combination therapy
- south africa
- endothelial cells
- adipose tissue
- stem cells
- small molecule
- randomized controlled trial