Pretreatment with Cry1Ac protoxin modulates the immune response, and increases the survival of Plasmodium-infected CBA/Ca mice

J Biomed Biotechnol. 2010:2010:198921. doi: 10.1155/2010/198921. Epub 2010 Mar 11.

Abstract

Malaria is a major global health problem that kills 1-2 million people each year. Despite exhaustive research, naturally acquired immunity is poorly understood. Cry1A proteins are potent immunogens with adjuvant properties and are able to induce strong cellular and humoral responses. In fact, it has been shown that administration of Cry1Ac protoxin alone or with amoebic lysates induces protection against the lethal infection caused by the protozoa Naegleria fowleri. In this work, we studied whether Cry1Ac is able to activate the innate immune response to induce protection against Plasmodium berghei ANKA (lethal) and P. chabaudi AS (nonlethal) parasites in CBA/Ca mice. Treatment with Cry1Ac induced protection against both Plasmodium species in terms of reduced parasitaemia, longer survival time, modulation of pro- and anti-inflammatory cytokines, and increased levels of specific antibodies against Plasmodium. Understanding how to boost innate immunity to Plasmodium infection should lead to immunologically based intervention strategies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacillus thuringiensis Toxins
  • Bacterial Proteins / administration & dosage*
  • Cytokines / immunology*
  • Endotoxins / administration & dosage*
  • Female
  • Hemolysin Proteins / administration & dosage*
  • Immunity, Innate / drug effects*
  • Immunity, Innate / immunology*
  • Malaria / drug therapy*
  • Malaria / immunology*
  • Male
  • Mice
  • Mice, Inbred CBA
  • Premedication / methods*
  • Survival Rate
  • Treatment Outcome

Substances

  • Bacillus thuringiensis Toxins
  • Bacterial Proteins
  • Cytokines
  • Endotoxins
  • Hemolysin Proteins
  • insecticidal crystal protein, Bacillus Thuringiensis