Overcoming the challenges of siRNA activation of innate immunity: design better therapeutic siRNAs

Methods Mol Biol. 2015:1218:301-19. doi: 10.1007/978-1-4939-1538-5_19.

Abstract

RNA interference (RNAi) is a conserved regulatory mechanism of posttranscriptional gene silencing triggered by either endogenously (e.g. microRNAs) or exogenously double-stranded RNA as small interfering (si) RNAs. To date, the use of siRNA (21-nt) has become a standard laboratory tool to silence gene expression in mammalian cells in-vitro and in-vivo. The methodology also holds promise for treating a diversity of human diseases. However, one of the challenges of making siRNAs as therapeutic drugs includes the activation of innate immunity and silencing of unwanted genes. Therefore, the use of siRNAs in functional genomics and human therapies depends on the development of strategies to overcome siRNA unwanted effects. This chapter highlights some efficient strategies aimed at separating gene silencing from immunostimulation and improving siRNA gene silencing specificity.

Publication types

  • Review

MeSH terms

  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology
  • Cancer Vaccines / administration & dosage
  • Cancer Vaccines / genetics
  • Cancer Vaccines / immunology*
  • Dendritic Cells / immunology*
  • Dendritic Cells / transplantation
  • Gene Expression Regulation, Neoplastic*
  • Genetic Engineering / methods
  • Humans
  • Immunity, Innate
  • Immunotherapy / methods
  • Neoplasms / genetics
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • RNA, Double-Stranded
  • RNA, Small Interfering / chemical synthesis
  • RNA, Small Interfering / genetics*
  • RNA, Small Interfering / immunology
  • Receptors, Retinoic Acid / genetics
  • Receptors, Retinoic Acid / immunology
  • Ribose / metabolism
  • Toll-Like Receptor 7 / genetics
  • Toll-Like Receptor 7 / immunology
  • Toll-Like Receptor 8 / genetics
  • Toll-Like Receptor 8 / immunology
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / immunology
  • Transfection

Substances

  • Antigens, Neoplasm
  • Cancer Vaccines
  • PLAAT4 protein, human
  • RNA, Double-Stranded
  • RNA, Small Interfering
  • Receptors, Retinoic Acid
  • TLR7 protein, human
  • TLR8 protein, human
  • Toll-Like Receptor 7
  • Toll-Like Receptor 8
  • Toll-Like Receptors
  • Ribose