Inhibitory mechanism of ternary fusion protein MSIK on HPV virus

H-F Hu1, Q-H Zhao, Y-F Sang

  • 1Affiliated Hospital, Hunan Polytechnic of Environment and Biology, Hengyang, China. huhengfenfen@126.com.

Abstract

Insights

The novel ternary fusion protein, MBP-SERPINA3-IFN-κ (MSIK), demonstrates significant potential in inhibiting human papillomavirus (HPV) replication and promoting wound healing. Further research confirms its efficacy in preventing viral influx and replication.

Area of Science:

  • Virology
  • Immunology
  • Biochemistry

Background:

  • Human papillomavirus (HPV) infections are a significant global health concern.
  • Current treatments for HPV infections have limitations, necessitating the development of novel therapeutic agents.
  • The ternary fusion protein MBP-SERPINA3-IFN-κ (MSIK) has been engineered for potential antiviral applications.

Purpose of the Study:

  • To investigate the efficacy of MSIK in inhibiting HPV proliferation.
  • To elucidate the underlying mechanisms of MSIK's antiviral activity against HPV.
  • To evaluate MSIK's impact on wound healing in a preclinical model.

Main Methods:

  • MSIK protein was prepared in various concentrations.
  • Epithelial cells and 300 mice were utilized in the study.
  • Herpes simplex virus type 1 (HSV-1) was used to model viral infection, and viral content was quantified using PCR.

Main Results:

  • MSIK demonstrated dose-dependent inhibition of HSV-1 invasion and replication in epithelial cells.
  • MSIK significantly accelerated wound healing in mice.
  • Higher concentrations of MSIK correlated with enhanced inhibition of HSV-1 invasion.

Conclusions:

  • MSIK exhibits potent antiviral properties, effectively inhibiting viral replication and preventing viral influx.
  • MSIK demonstrates a dual therapeutic effect, promoting wound healing while combating viral infections.
  • MSIK shows promise as a therapeutic agent for the prevention and treatment of HPV infections.

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