| Literature DB >> 29650384 |
Marcin Smreczak1, Anna Orłowska2, Anna Marzec2, Paweł Trębas2, Anna Kycko2, Michał Reichert2, Penelope Koraka3, Albert D M E Osterhaus4, Jan Franciszek Żmudziński2.
Abstract
Rabies is a fatal disease of all mammals causing almost 60,000 human deaths every year. To date, there is no effective treatment of clinical rabies once the symptoms appear. Here, we describe the promising effect of combination therapy composed of molecules that target replication of the rabies virus (RV) at different stages of life cycle and molecules that inhibit some pathways of the innate host immune response accompanied by a blood-brain barrier opener on the outcome of RV infection. The study reports statistically significant extension of survival of mice treated with the drug cocktail containing T-705, ribavirin, interferon α/β, caspase-1 inhibitor, TNF-α inhibitor, MAPKs inhibitor and HRIG compared to the survival of mice in the virus control group (p = 0.0312). Furthermore, the study points to the significant impact of interferon α/β on the survival of RV-infected mice. We have shown a significant down regulation of pro-inflammatory molecules (caspase-1 and TNF-a) in the CNS in RV-infected mice treated with a combination of drugs including interferon α/β.Entities:
Keywords: Antivirals; Clinical rabies; Host immune response modulators; Interferon α/β; SHBRV-18
Year: 2018 PMID: 29650384 DOI: 10.1016/j.vaccine.2018.04.003
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641