Rationally designed synthetic vectors for therapeutic nucleic acid delivery against human cytomegalovirus infection

J Med Virol. 2023 Mar;95(3):e28586. doi: 10.1002/jmv.28586.

Abstract

RNA therapy represents a great way to precisely regulate cellular processes by modulating the gene expression. Despite this potential, a profound gap exists in our knowledge of how to subsequently deliver these RNAs into the specific target cells and turn therapeutically active RNAs into practical medicines. An advanced series of interlocked, thermodynamically self-regulated processes that enable the precise assembly of functional synthetic carriers of siRNA to the target cells in vivo was developed. To demonstrate the efficacy of this delivery system, we used it to treat human cytomegalovirus (HCMV) infection in a humanized mouse model. In this study, we use small interfering RNA (siRNA) and small complementary RNA (scRNA) to inhibit the expressions of two HCMV genes, IE1 and IE2. The auto-regulated nanocarrier polywraplex with core-shell structure was designed to condense and package these RNAs for delivering. To allow these particles recognize the HCMV-infected cells, a ligand was coupled on the surface of nanoparticle, which would specifically target the HCMV-encoded CX3 CL1 chemokine receptor presented in the HCMV-infected cells. The results demonstrated that the polywraplex conjugated with the target molecule CX3 CL1 effectively and specifically delivered the siRNA/scRNA to HCMV infected cells and inhibited virus growth in vitro and in vivo.

Keywords: chemokine; human cytomegalovirus infection; nanoparticle; surface-assembly; synthetic carrier of nucleic acid.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytomegalovirus / genetics
  • Cytomegalovirus Infections* / genetics
  • Cytomegalovirus Infections* / therapy
  • Humans
  • Immediate-Early Proteins* / genetics
  • Mice
  • Nucleic Acids*
  • RNA, Small Interfering / genetics
  • Trans-Activators / genetics

Substances

  • Immediate-Early Proteins
  • Trans-Activators
  • Nucleic Acids
  • RNA, Small Interfering