Malaria Journal

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Schistosoma mansoni infection reduces the incidence of murine cerebral malaria

Judith H Waknine-Grinberg1,2, Daniel Gold3, Ariel Ohayon4, Eliezer Flescher3, Alina Heyfets3, Michael J Doenhoff5, Gabriele Schramm6, Helmut Haas6 and Jacob Golenser1*

Author Affiliations

1 Department of Microbiology and Molecular Genetics, The Hebrew University of Jerusalem, Jerusalem, Israel, 91120

2 Laboratory of Membrane and Liposome Research, Department of Biochemistry, The Hebrew University of Jerusalem, Israel

3 Department of Clinical Microbiology and Immunology, Sackler School of Medicine, Tel Aviv University, Israel

4 Shraga Segal Department of Microbiology and Immunology, Ben-Gurion University of the Negev, Beer-Sheva, Israel

5 The School of Biology, The University of Nottingham, Nottingham, UK

6 Research Center Borstel, Borstel, Germany

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Malaria Journal 2010, 9:5 doi:10.1186/1475-2875-9-5

Published: 5 January 2010

Abstract

Background

Plasmodium and Schistosoma are two of the most common parasites in sub-tropical areas. Deregulation of the immune response to Plasmodium falciparum, characterized by a Th1 response, leads to cerebral malaria (CM), while a Th2 response accompanies chronic schistosomiasis.

Methods

The development of CM was examined in mice with concomitant Schistosoma mansoni and Plasmodium berghei ANKA infections. The effect of S. mansoni egg antigen injection on disease development and survival was also determined. Cytokine serum levels were estimated using ELISA. Statistical analysis was performed using t-test.

Results

The results demonstrate that concomitant S. mansoni and P. berghei ANKA infection leads to a reduction in CM. This effect is dependent on infection schedule and infecting cercariae number, and is correlated with a Th2 response. Schistosomal egg antigen injection delays the death of Plasmodium-infected mice, indicating immune involvement.

Conclusions

This research supports previous claims of a protective effect of helminth infection on CM development. The presence of multiple parasitic infections in patients from endemic areas should therefore be carefully noted in clinical trials, and in the development of standard treatment protocols for malaria. Defined helminth antigens may be considered for alleviation of immunopathological symptoms.