Targeting the master regulator mTOR: A new approach to prevent the neurological of consequences of parasitic infections?
- Publication Type:
- Journal Article
- Citation:
- Parasites and Vectors, 2017, 10 (1)
- Issue Date:
- 2017-11-21
Open Access
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author |
Donnelly, S |
en_US |
dc.contributor.author |
Huston, WM |
en_US |
dc.contributor.author | Johnson, M | en_US |
dc.contributor.author |
Tiberti, N |
en_US |
dc.contributor.author |
Saunders, B |
en_US |
dc.contributor.author |
O'Brien, B |
en_US |
dc.contributor.author |
Burke, C |
en_US |
dc.contributor.author |
Labbate, M |
en_US |
dc.contributor.author |
Combes, V |
en_US |
dc.date.available | 2017-11-09 | en_US |
dc.date.issued | 2017-11-21 | en_US |
dc.identifier.citation | Parasites and Vectors, 2017, 10 (1) | en_US |
dc.identifier.uri | http://hdl.handle.net/10453/122245 | |
dc.description.abstract | © 2017 The Author(s). A systematic analysis of 240 causes of death in 2013 revealed that parasitic diseases were responsible for more than one million deaths. The vast majority of these fatalities resulted from protozoan infections presenting with neurological sequelae. In the absence of a vaccine, development of effective therapies is essential to improving global public health. In 2015, an intriguing strategy to prevent cerebral malaria was proposed by Gordon et al. 2015 mBio, 6:e00625. Their study suggested that inhibition of the mammalian target of rapamycin prevented experimental cerebral malaria by blocking the damage to the blood brain barrier and stopping the accumulation of parasitized red blood cells and T cells in the brain. Here, we hypothesize that the same therapeutic strategy could be adopted for other protozoan infections with a brain tropism, to prevent cerebral parasitosis by limiting pathogen replication and preventing immune mediated destruction of brain tissue. | en_US |
dc.relation.ispartof | Parasites and Vectors | en_US |
dc.relation.isbasedon | 10.1186/s13071-017-2528-3 | en_US |
dc.subject.classification | Mycology & Parasitology | en_US |
dc.subject.classification | Tropical Medicine | en_US |
dc.subject.mesh | Blood-Brain Barrier | en_US |
dc.subject.mesh | Brain | en_US |
dc.subject.mesh | Erythrocytes | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Mice | en_US |
dc.subject.mesh | Plasmodium berghei | en_US |
dc.subject.mesh | Parasitic Diseases | en_US |
dc.subject.mesh | Central Nervous System Protozoal Infections | en_US |
dc.subject.mesh | Malaria, Cerebral | en_US |
dc.subject.mesh | Sirolimus | en_US |
dc.subject.mesh | Immunosuppressive Agents | en_US |
dc.subject.mesh | Drug Design | en_US |
dc.subject.mesh | TOR Serine-Threonine Kinases | en_US |
dc.title | Targeting the master regulator mTOR: A new approach to prevent the neurological of consequences of parasitic infections? | en_US |
dc.type | Journal Article | |
utslib.citation.volume | 1 | en_US |
utslib.citation.volume | 10 | en_US |
utslib.for | 1108 Medical Microbiology | en_US |
utslib.for | 1117 Public Health and Health Services | en_US |
pubs.embargo.period | Not known | en_US |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
pubs.organisational-group | /University of Technology Sydney/Strength - CHT - Health Technologies | |
utslib.copyright.status | open_access | |
pubs.issue | 1 | en_US |
pubs.publication-status | Published | en_US |
pubs.volume | 10 | en_US |
Abstract:
© 2017 The Author(s). A systematic analysis of 240 causes of death in 2013 revealed that parasitic diseases were responsible for more than one million deaths. The vast majority of these fatalities resulted from protozoan infections presenting with neurological sequelae. In the absence of a vaccine, development of effective therapies is essential to improving global public health. In 2015, an intriguing strategy to prevent cerebral malaria was proposed by Gordon et al. 2015 mBio, 6:e00625. Their study suggested that inhibition of the mammalian target of rapamycin prevented experimental cerebral malaria by blocking the damage to the blood brain barrier and stopping the accumulation of parasitized red blood cells and T cells in the brain. Here, we hypothesize that the same therapeutic strategy could be adopted for other protozoan infections with a brain tropism, to prevent cerebral parasitosis by limiting pathogen replication and preventing immune mediated destruction of brain tissue.
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