Therapeutic Use of Native and Recombinant Enteroviruses

Jani Ylä-Pelto1, Lav Tripathi2, Petri Susi3,4

  • 1Department of Virology, University of Turku, Kiinamyllynkatu 13, 20520 Turku, Finland. jani.ylapelto@gmail.com.

Viruses
|February 25, 2016
PubMed

Insights

Human enteroviruses, which infect cells via specific receptors often overexpressed in cancers, show potential for oncolytic virotherapy. Modifications to enterovirus genomes create therapeutic vectors for cancer treatment and vaccine development.

Area of Science:

  • Virology
  • Oncology
  • Gene Therapy

Background:

  • Over 100 human enterovirus types identified, utilizing specific protein receptors for cell entry and replication.
  • Many viral receptors are overexpressed in cancer cells, influencing viral tropism and pathogenesis.
  • Enteroviruses induce cytolytic responses, disrupting infected cells, making them candidates for oncolytic virotherapy.

Purpose of the Study:

  • To review the therapeutic applications of native and recombinant enteroviruses.
  • To explore methods for modifying enterovirus genomes for therapeutic purposes.
  • To highlight the potential of enteroviruses in oncolytic virotherapy and vaccine development.

Main Methods:

  • Identification and characterization of enterovirus types and their receptors.
  • Analysis of viral tropism and cytolytic properties.
  • Copy DNA cloning and genetic modification of enterovirus genomes to create vectors.

Main Results:

  • Enteroviruses exhibit tropism and cytolytic activity, making them suitable for oncolytic virotherapy.
  • Engineered enterovirus vectors can express foreign antigenic epitopes for vaccine trials.
  • Enterovirus genome modification is constrained by small genome size and particle structure.

Conclusions:

  • Native and engineered enteroviruses hold significant promise for cancer treatment (oncolytic virotherapy).
  • Enterovirus-based vectors are valuable tools for vaccine development.
  • Further research into enterovirus genome modification is needed to optimize therapeutic potential.