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In Vitro Inhibition of Plasmodium falciparum Rosette Formation by Curdlan Sulfate

Authors :
J. Alexandra Rowe
Peter C. Bull
Mònica Arman
Helen M. Kyriacou
Ahmed Raza
Ivan Havlik
Katie E. Steen
George M. Warimwe
Source :
Kyriacou, H M, Steen, K E, Raza, A, Arman, M, Warimwe, G, Bull, P C, Havlik, I & Rowe, J A 2007, ' In vitro inhibition of Plasmodium falciparum rosette formation by Curdlan sulfate ', Antimicrobial Agents and Chemotherapy, vol. 51, no. 4, pp. 1321-6 . https://doi.org/10.1128/AAC.01216-06
Publication Year :
2007
Publisher :
American Society for Microbiology, 2007.

Abstract

Spontaneous binding of infected erythrocytes to uninfected erythrocytes to form rosettes is a property of some strains of Plasmodium falciparum that is linked to severe complications of malaria. Curdlan sulfate (CRDS) is a sulfated glycoconjugate compound that is chemically similar to known rosette-inhibiting drugs such as heparin. CRDS has previously been shown to have antimalarial activity in vitro and is safe for clinical use. Here we show that CRDS at therapeutic levels (10 to 100 μg/ml) significantly reduces rosette formation in vitro in seven P. falciparum laboratory strains and in a group of 18 African clinical isolates. The strong ability to inhibit rosetting suggests that CRDS has the potential to reduce the severe complications and mortality rates from P. falciparum malaria among African children. Our data support further clinical trials of CRDS.

Details

ISSN :
10986596 and 00664804
Volume :
51
Database :
OpenAIRE
Journal :
Antimicrobial Agents and Chemotherapy
Accession number :
edsair.doi.dedup.....6241d99370bf0d71e09d0ec5477cb729
Full Text :
https://doi.org/10.1128/aac.01216-06