Host response to cytoadherence inPlasmodium falciparum

Chakravorty, Srabasti J.; Hughes, Katie R.; Craig, Alister G.

Abstract

Cytoadherence of PRBCs (Plasmodium falciparum-infected red blood cells) to host endothelium has been associated with pathology in severe malaria, but, despite extensive information on the primary processes involved in the adhesive interactions, the mechanisms underlying the disease are poorly understood. Endothelial cells have the ability to mobilize immune and pro-adhesive responses when exposed to both PRBCs and TNF (tumour necrosis factor). In addition, there is also an up-regulation by PRBCs and TNF and a concurrent down-regulation of a range of genes involved in inflammation and cell death, by PRBCs and TNF. We propose that the balance between positive and negative regulation will contribute to endothelial pathology during malarial infection. Apposition of PRBCs has been shown by a number of groups to activate signalling pathways. This is dependent, at least in part, on the cytoadherence characteristics of the invading isolate, such that the avidity of the PRBC for the receptor on host endothelium is proportional to the level of activation of the signalling pathways. An understanding of the post-adhesive processes produced by cytoadherence may help us to understand the variable pathology seen in malaria and to design appropriate therapies to alleviate severe disease.

Citation

Chakravorty, S., Hughes, K., & Craig, A. (2008). Host response to cytoadherence inPlasmodium falciparum. Biochemical Society Transactions, 36(2), 221-228. https://doi.org/10.1042/bst0360221

• Journal Article Type: Article
• Online Publication Date: Mar 20, 2008
• Publication Date: Apr 1, 2008
• Deposit Date: May 14, 2024
• Journal: Biochemical Society Transactions
• Print ISSN: 0300-5127
• Electronic ISSN: 1470-8752
• Publisher: Portland Press
• Peer Reviewed: Peer Reviewed
• Volume: 36
• Issue: 2
• Pages: 221-228
• DOI: https://doi.org/10.1042/bst0360221
• Keywords: adhesion, endothelium, malaria, Plasmodium falciparum, signalling, var gene
• Public URL: https://keele-repository.worktribe.com/output/827367