| Literature DB >> 30349030 |
Joshua A Jackman1, Vivian V Costa2,3,4, Soohyun Park1, Ana Luiza C V Real5, Jae Hyeon Park1, Pablo L Cardozo5, Abdul Rahim Ferhan1, Isabella G Olmo5, Thaiane P Moreira4,6, Jordana L Bambirra4,6, Victoria F Queiroz4,6, Celso M Queiroz-Junior7, Giselle Foureaux7, Danielle G Souza6, Fabiola M Ribeiro5, Bo Kyeong Yoon1, Evelien Wynendaele8, Bart De Spiegeleer8, Mauro M Teixeira2,3, Nam-Joon Cho9,10.
Abstract
Zika virus is a mosquito-borne virus that is associated with neurodegenerative diseases, including Guillain-Barré syndrome1 and congenital Zika syndrome2. As Zika virus targets the nervous system, there is an urgent need to develop therapeutic strategies that inhibit Zika virus infection in the brain. Here, we have engineered a brain-penetrating peptide that works against Zika virus and other mosquito-borne viruses. We evaluated the therapeutic efficacy of the peptide in a lethal Zika virus mouse model exhibiting systemic and brain infection. Therapeutic treatment protected against mortality and markedly reduced clinical symptoms, viral loads and neuroinflammation, as well as mitigated microgliosis, neurodegeneration and brain damage. In addition to controlling systemic infection, the peptide crossed the blood-brain barrier to reduce viral loads in the brain and protected against Zika-virus-induced blood-brain barrier injury. Our findings demonstrate how engineering strategies can be applied to develop peptide therapeutics and support the potential of a brain-penetrating peptide to treat neurotropic viral infections.Entities:
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Year: 2018 PMID: 30349030 DOI: 10.1038/s41563-018-0194-2
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841