Cytoadherence characteristics of Plasmodium falciparum isolates in Thailand using an in vitro human lung endothelial cells model

Am J Trop Med Hyg. 2000 Jan;62(1):38-44. doi: 10.4269/ajtmh.2000.62.38.

Abstract

Using an in vitro model of human lung endothelial cells, we studied different characteristics of Plasmodium falciparum isolates as potential factors for malaria severity in 2 Thai patient groups: 27 with complicated malaria and 42 with uncomplicated malaria. In regard to binding properties, no association existed between cytoadherence and rosette phenotypes (P = 0.1) and hypothrombocytemia increased the cytoadherence level (P = 0.007). Cytoadherence was significantly associated with malaria severity (P = 0.05) in contrast to rosette formation (P = 0.9). Intercellular adhesion molecule-1 and chondroitin-4-sulfate were major receptors of cytoadherence in those with complicated malaria compared with those with uncomplicated malaria (P < 10(-4)). Chondroitin-4-sulfate could act as a putative receptor for malaria complications in non-pregnant women. CD36 was the main receptor in patients with uncomplicated malaria (P < 10(-3)). Vascular cell adhesion molecule-1 and E-selectin played a minor role in 2 groups (P = 0.6). Qinghaosu derivatives were more efficient than other antimalarial drugs, but a positive correlation was observed between the 50% inhibitory concentrations of halofantrine and quinine and the number of adhesive parasitized red blood cells, suggesting their influence on cytoadherence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Antibodies, Monoclonal
  • Antimalarials / pharmacology
  • Binding, Competitive / physiology
  • Cell Adhesion / physiology
  • Cells, Cultured
  • Chondroitin Sulfates / physiology
  • Endothelium / pathology
  • Female
  • Humans
  • Intercellular Adhesion Molecule-1 / physiology
  • Lung / pathology*
  • Malaria, Falciparum / pathology*
  • Male
  • Middle Aged
  • Parasitemia
  • Phenanthrenes / pharmacology
  • Plasmodium falciparum / chemistry*
  • Quinine / administration & dosage
  • Quinine / therapeutic use
  • Rosette Formation
  • Thailand

Substances

  • Antibodies, Monoclonal
  • Antimalarials
  • Phenanthrenes
  • Intercellular Adhesion Molecule-1
  • Chondroitin Sulfates
  • Quinine
  • halofantrine