Immunomodulator effect of picroliv and its potential in treatment against resistant Plasmodium yoelii (MDR) infection in mice

Pharm Res. 2008 Oct;25(10):2312-9. doi: 10.1007/s11095-008-9631-2. Epub 2008 Jun 13.

Abstract

Purpose: The present study was envisaged to evaluate potential of combination therapy comprising of immunomodulator picroliv and antimalarial chloroquine against drug resistant Plasmodium yoelii (P. yoelii) infection in BALB/c mice.

Methods: The immunomodulatory potential of picroliv was established by immunizing animals with model antigen along with picroliv. Immune response was assessed using T-cell proliferation assay and also by determining the antibody isotype-profile induced in the immunized mice. In the next set of experiment, prophylactic potential of picroliv to strengthen antimalarial properties of chloroquine against P. yoelii (MDR) infection in BALB/c mice was assessed.

Results: T-cell proliferation as well as antibody production study reveals that picroliv helps in evoking strong immuno-potentiating response against model antigen in the immunized mice. Co-administration of picroliv enhances efficacy of CHQ against experimental murine malaria.

Conclusion: The activation of host immune system can increase the efficacy of chloroquine for suppression of drug resistant malaria infection in BALB/c mice.

MeSH terms

  • Animals
  • Antimalarials / pharmacology*
  • B7-1 Antigen / metabolism
  • B7-2 Antigen / metabolism
  • Chloroquine / pharmacology*
  • Cinnamates / pharmacology*
  • Drug Resistance, Multiple*
  • Drug Therapy, Combination
  • Female
  • Glycosides / pharmacology*
  • Immunoglobulin G / blood
  • Immunologic Factors / pharmacology*
  • Lymphocyte Activation / drug effects
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Malaria / drug therapy*
  • Malaria / immunology
  • Malaria / parasitology
  • Mice
  • Mice, Inbred BALB C
  • Ovalbumin / immunology
  • Plasmodium yoelii / drug effects*
  • Plasmodium yoelii / immunology
  • Reactive Oxygen Species / metabolism
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • Time Factors
  • Up-Regulation
  • Vanillic Acid / pharmacology*

Substances

  • Antimalarials
  • B7-1 Antigen
  • B7-2 Antigen
  • Cd86 protein, mouse
  • Cinnamates
  • Glycosides
  • Immunoglobulin G
  • Immunologic Factors
  • Reactive Oxygen Species
  • kutkin
  • Chloroquine
  • Ovalbumin
  • Vanillic Acid