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Novel treatment protects mice against malaria; approach may work in humans as well

Malaria is a major global health concern, and researchers are in need of new therapeutic approaches. To address this concern, a study published Oct. 26 in the online journal PLoS ONE reveals new information about the host cell's treatment of the parasite that causes the disease in mice, opening potential new avenues for research and treatment.

The new work, led by Hernando del Portillo of the Barcelona Centre for International Health Research, used a mouse model of malaria infection to detect parasite proteins in small vesicles produced by a variety of mammalian cells called exosomes.

These vesicles had recently been shown to be involved in the immune response to a number of infections, and therefore of potential interest for therapeutic approaches, but their connection to malaria had not been previously investigated.

In the new study, the researchers found that reticulocyte-derived exosomes (rex) are involved in the malaria infection, and they also showed that rex containing parasite proteins could be used to immunize mice, resulting in full protection upon lethal infections in 85% of the animals. While the work up to this point has been limited to a mouse model of the malaria parasite, the authors suggest that the results present new possible directions for the development of novel anti-malaria treatments, specifically against the human malaria parasite P. vivax which has a unique cell tropism for reticulocytes, the original cells where exosomes were discovered.




Citation: Martin-Jaular L, Nakayasu ES, Ferrer M, Almeida IC, del Portillo HA (2011) Exosomes from Plasmodium yoelii-Infected Reticulocytes Protect Mice from Lethal Infections. PLoS ONE 6(10): e26588. doi:10.1371/journal.pone.0026588

Financial Disclosure: MF is a recipient of a graduate fellowship from the Generalitat de Catalonia. ICA was partially supported by National Institutes of Health (NIH) grants Nos 5G12RR008124-16A1 and 5G12RR008124-16A1S1. The biomedical Analysis Care Facility/BBRC/UTEP is funded by NIH grants 5G12RR008124-16A1 and 5G12RR008124-16A1S1. HAP is an ICREA Research Professor. Work in the laboratory of HAP is funded by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement Nu 242095, by the Private Foundation CELLEX (Catalonia, Spain), and by the Spanish Ministry of Science and Innovation (SAF2009-07760). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interest Statement: The authors have declared that no competing interests exist.

Disclaimer: This press release refers to upcoming articles in PLoS ONE. The releases have been provided by the article authors and/or journal staff. Any opinions expressed in these are the personal views of the contributors, and do not necessarily represent the views or policies of PLoS. PLoS expressly disclaims any and all warranties and liability in connection with the information found in the release and article and your use of such information.

About PLoS ONE

PLoS ONE is the first journal of primary research from all areas of science to employ a combination of peer review and post-publication rating and commenting, to maximize the impact of every report it publishes. PLoS ONE is published by the Public Library of Science (PLoS), the open-access publisher whose goal is to make the world's scientific and medical literature a public resource.

All works published in PLoS ONE are Open Access. Everything is immediately available—to read, download, redistribute, include in databases and otherwise use—without cost to anyone, anywhere, subject only to the condition that the original authors and source are properly attributed. For more information about PLoS ONE relevant to journalists, bloggers and press officers, including details of our press release process and our embargo policy, see the everyONE blog at

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