Combination of paromomycin and miltefosine promotes TLR4-dependent induction of antileishmanial immune response in vitro

J Antimicrob Chemother. 2012 Oct;67(10):2373-8. doi: 10.1093/jac/dks220. Epub 2012 Jul 3.

Abstract

Objectives: To evaluate the in vitro activity of antileishmanial drugs, paromomycin and miltefosine, to generate Th-1-biased immunomodulation in hosts against intracellular Leishmania donovani.

Methods: In silico protein-ligand interaction and in vitro drug-cell interaction assays were performed. Interaction assays of TLR4-deficient HEK293 cells and HEK293 cells engineered to express either TLR4 or TLR2 with different concentrations of miltefosine and/or paromomycin sulphate were performed for 48 h. Differentially transfected human peripheral blood monocyte-derived macrophages (PBMFs) were treated with the drugs, and nuclear factor (NF)-κB promoter activity was measured using a κB-luciferase reporter construct. PBMFs were infected with L. donovani. Cultures were incubated with miltefosine or paromomycin sulphate over different concentrations, as mono-treatment or combined. The in vitro antileishmanial effect of the drugs on macrophage-bound L. donovani amastigotes was measured in terms of parasite killing and production of tumour necrosis factor-α (TNF-α) and nitric oxide.

Results: Computational studies reveal that paromomycin and miltefosine interact with TLR4. Both drugs, as monotherapy or in combination, induce release of TNF-α and nitric oxide in a TLR4-dependent manner. Interestingly, the TLR4-dependent action of the drugs leads to NF-κB promoter activation through MyD88. In vitro, both the drugs kill macrophage-bound L. donovani by inducing release of TNF-α and nitric oxide in a TLR4-dependent manner.

Conclusions: The in vitro activity of paromomycin and miltefosine against host cells is TLR4 dependent. This has implications for: (i) evaluation of in vitro activity of combinational antileishmanial therapy; (ii) the evaluation of drug susceptibility of clinical isolates; and (iii) the standardization of in vitro antileishmanial assays for determining toxicity in hosts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antiprotozoal Agents / pharmacology*
  • Artificial Gene Fusion
  • Cell Survival
  • Cells, Cultured
  • Female
  • Gene Expression Profiling
  • Genes, Reporter
  • Humans
  • Immunologic Factors / pharmacology*
  • Leishmania donovani / immunology*
  • Luciferases / analysis
  • Luciferases / genetics
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / parasitology
  • Male
  • NF-kappa B / biosynthesis
  • Nitric Oxide / metabolism
  • Paromomycin / pharmacology*
  • Phosphorylcholine / analogs & derivatives*
  • Phosphorylcholine / pharmacology
  • Toll-Like Receptor 4 / agonists*
  • Tumor Necrosis Factor-alpha / metabolism
  • Young Adult

Substances

  • Antiprotozoal Agents
  • Immunologic Factors
  • NF-kappa B
  • TLR4 protein, human
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Phosphorylcholine
  • Nitric Oxide
  • miltefosine
  • Paromomycin
  • Luciferases