Furin-dependent CCL17-fused recombinant toxin controls HTLV-1 infection by targeting and eliminating infected CCR4-expressing cells in vitro and in vivo

Retrovirology. 2015 Aug 20:12:73. doi: 10.1186/s12977-015-0199-8.

Abstract

Background: Adult T-cell leukemia (ATL) is caused by human T-cell leukemia virus type 1 (HTLV-1) infection. However, there are no therapies to prevent ATL development in high-risk asymptomatic carriers. To develop a therapy targeting HTLV-1-infected cells that are known to express CCR4 frequently, we tested whether truncated Pseudomonas exotoxin (PE38) fused to a CCR4 ligand, CCL17/thymus and activation-regulated chemokine (TARC), selectively eliminates such cells.

Results: Our data show that TARC-PE38 efficiently killed HTLV-1-infected cell lines. It also shrank HTLV-1-associated solid tumors in an infected-cell-engrafted mouse model. In HTLV-1-positive humanized mice, TARC-PE38 markedly inhibited the proliferation of HTLV-1-infected human CD4(+)CD25(+) or CD4(+)CD25(+)CCR4(+) cells and reduced the proviral loads (PVLs) in peripheral blood mononuclear cells (PBMCs). Importantly, TARC-PE38 significantly reduced the PVLs in PBMCs obtained from asymptomatic carriers. We show that the cytotoxicity of TARC-PE38 is mediated by the expression of the proprotein convertase, furin. The expression of furin was enhanced in HTLV-1-infected cells and correlated positively with PVLs in HTLV-1-infected individuals, suggesting that infected cells are more susceptible to TARC-PE38 than normal cells.

Conclusions: TARC-PE38 robustly controls HTLV-1 infection by eliminating infected cells in both a CCR4- and furin-dependent manner, indicating the excellent therapeutic potential of TARC-PE38.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Asymptomatic Infections / therapy
  • Cell Line, Tumor
  • Chemokine CCL17 / pharmacology*
  • Chemokines / genetics
  • Disease Models, Animal
  • Exotoxins / pharmacology*
  • Furin / genetics*
  • Furin / pharmacology*
  • Human T-lymphotropic virus 1 / drug effects*
  • Human T-lymphotropic virus 1 / growth & development
  • Humans
  • Jurkat Cells
  • Leukemia-Lymphoma, Adult T-Cell / drug therapy*
  • Leukemia-Lymphoma, Adult T-Cell / virology*
  • Leukocytes, Mononuclear / virology
  • Mice
  • Proviruses / drug effects
  • Proviruses / physiology
  • Receptors, CCR4 / genetics
  • Receptors, CCR4 / metabolism*
  • Recombinant Fusion Proteins / pharmacology*
  • U937 Cells

Substances

  • Chemokine CCL17
  • Chemokines
  • Exotoxins
  • Receptors, CCR4
  • Recombinant Fusion Proteins
  • TARC-PE38 fusion protein
  • Furin