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Murine cerebral malaria development is independent of Toll-like receptor signaling


Togbe, D; Schofield, L; Grau, GE; Schnyder, B; Boissay, V; Charron, S; Rose, S; Beutler, B; Quesniaux, VFJ; Ryffel, B
2007-05
AMERICAN JOURNAL OF PATHOLOGY
Journal Article
170
5
1640-1648
Malaria pigment hemozoin was reported to activate the innate immunity by Toll-like receptor (TLR)-9 engagement. However, the role of TLR activation for the development of cerebral malaria (CM), a lethal complication of malaria infection in humans, is unknown. Using Plasmodium berghei ANKA (PbA) infection in mice as a model of CM, we report here that TLR9-deficient mice are not protected from CM. To exclude the role of other members of the TLR family in PbA recognition, we infected mice deficient for single TLR1, -2, -3, -4, -6, -7, or -9 and their adapter proteins MyD88, TIRAP, and TRIF. In contrast to lymphotoxin a-deficient mice, which are resistant to CM, all TLR-deficient mice were as sensitive to fatal CM development as wild-type control mice and developed typical microvascular damage with vascular leak and hemorrhage in the brain and lung, together with comparable parasitemia, thrombocytopenia, neutrophilia, and lymphopenia. In conclusion, the present data do not exclude the possibility that malarial molecular motifs may activate the innate immune system. However, TLR-dependent activation of innate immunity is unlikely to contribute significantly to the proinflammatory response to PbA infection and the development of fatal CM.
AMER SOC INVESTIGATIVE PATHOLOGY, INC
PLASMODIUM-BERGHEI INFECTION; DOUBLE-STRANDED-RNA; LYMPHOTOXIN-ALPHA; INNATE IMMUNITY; DEFICIENT MICE; CUTTING EDGE; FALCIPARUM; ACTIVATION; RESPONSES; GLYCOSYLPHOSPHATIDYLINOSITOL
10.2353/ajpath.2007.060889
Refer to copyright notice on published article.

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Creation Date 2007-05-01 12:00:00