Antiviral effects of liposome-encapsulated PolyICLC against Dengue virus in a mouse model

Biochem Biophys Res Commun. 2016 Sep 16;478(2):913-8. doi: 10.1016/j.bbrc.2016.08.050. Epub 2016 Aug 11.

Abstract

This study presents the first investigation of the antiviral effects of the liposome-encapsulated PolyICLC (LE-PolyICLC) on Dengue virus (DENV) in a mouse model. In vivo efficacy studies showed that LE-PolyICLC acted to increase antiviral mechanisms mainly through promoting cytokine expression associated with innate immunity, such as IFN-γ. In addition, the pro-inflammatory cytokine TNF-α was also increased, while IL-6 level was decreased in serum. The titers of total antibodies against DENV2 in mice were also elevated. Administration of LE-PolyICLC not only alleviated the loss of body weight, degree of morbidity, and pathological damage in brains, but also reduced the viral titers and expression of viral E protein in the brain. Notably, the effectiveness of LE-PolyICLC was better than PolyICLC on the basis of the data presented in this study. These results, therefore, set a foundation for further development of LE-PolyICLC as an attractive candidate of antiviral agents to be used in both prophylactic and therapeutic settings in DENV diseases.

Keywords: Antiviral; Dengue 2 virus; Innate immunity; LE-PolyICLC.

MeSH terms

  • Animals
  • Antibody Formation / drug effects
  • Antigens, Viral / metabolism
  • Antiviral Agents / pharmacology*
  • Antiviral Agents / therapeutic use*
  • Brain / pathology
  • Carboxymethylcellulose Sodium / analogs & derivatives*
  • Carboxymethylcellulose Sodium / pharmacology
  • Carboxymethylcellulose Sodium / therapeutic use
  • Cytokines / metabolism
  • Dengue / drug therapy*
  • Dengue / virology*
  • Dengue Virus / drug effects*
  • Disease Models, Animal
  • Liposomes
  • Mice
  • Mice, Inbred BALB C
  • Poly I-C / pharmacology*
  • Poly I-C / therapeutic use*
  • Polylysine / analogs & derivatives*
  • Polylysine / pharmacology
  • Polylysine / therapeutic use
  • RNA, Viral / metabolism
  • Virus Replication / drug effects

Substances

  • Antigens, Viral
  • Antiviral Agents
  • Cytokines
  • Liposomes
  • RNA, Viral
  • Polylysine
  • poly ICLC
  • Carboxymethylcellulose Sodium
  • Poly I-C