Literature DB >> 16603167

Conventional and experimental treatment of cerebral malaria.

J Golenser1, J McQuillan, L Hee, A J Mitchell, N H Hunt.   

Abstract

The most severe complication of Plasmodium falciparum infection is cerebral malaria (CM). Cerebral malaria implies the presence of neurological features, especially impaired consciousness. The treatment of CM is limited to: (i) a few conventional anti-malarial drugs (quinine or artemisinins), (ii) adjunctive treatments (initial stabilisation, blood exchange transfusion, osmotic diuretics and correction of hypoglycaemia, acidosis and hypovolaemia) and (iii) immunomodulation. There are clear procedures concerning treatment of CM, which include the use of the anti-plasmodial drugs. Adjunctive treatments are permissible but there is no single official guideline and immune intervention is a possibility currently being examined in rodent models only. The suggested immunomodulation approach is based on the strong likelihood that CM is the result of an immunopathological process. P. falciparum initiates the multifactorial chain of events leading to lethal CM and, after a certain stage, it is impossible to stop the progression even by using anti-malarial drugs. We present evidence that CM is a result of a dysregulated immune response. Therefore, it might be prevented by early modulation of discrete factors that participate in this process. In experimental systems, some immunomodulators delay or prevent CM without affecting the parasitaemia. Therefore, in the future the ultimate treatment of CM may be a combination of an anti-malarial and an immunomodulator. However, the overall effect of an immunomodulator would need to be carefully examined in view of concomitant infections, especially in malaria endemic areas.

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Year:  2006        PMID: 16603167     DOI: 10.1016/j.ijpara.2006.02.009

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  22 in total

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Authors:  L Clemmer; Y C Martins; G M Zanini; J A Frangos; L J M Carvalho
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4.  Differential microRNA expression in experimental cerebral and noncerebral malaria.

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Journal:  Infect Immun       Date:  2011-03-21       Impact factor: 3.441

5.  Structure-activity relationship and mechanism of action studies of manzamine analogues for the control of neuroinflammation and cerebral infections.

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6.  Cognitive dysfunction is sustained after rescue therapy in experimental cerebral malaria, and is reduced by additive antioxidant therapy.

Authors:  Patricia A Reis; Clarissa M Comim; Fernanda Hermani; Bruno Silva; Tatiana Barichello; Aline C Portella; Flavia C A Gomes; Ive M Sab; Valber S Frutuoso; Marcus F Oliveira; Patricia T Bozza; Fernando A Bozza; Felipe Dal-Pizzol; Guy A Zimmerman; João Quevedo; Hugo C Castro-Faria-Neto
Journal:  PLoS Pathog       Date:  2010-06-24       Impact factor: 6.823

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8.  Safety of epoietin beta-quinine drug combination in children with cerebral malaria in Mali.

Authors:  Stéphane Picot; Anne-Lise Bienvenu; Salimata Konate; Sibiri Sissoko; Abdoulaye Barry; Elisabeth Diarra; Karidiatou Bamba; Abdoulaye Djimdé; Ogobara K Doumbo
Journal:  Malar J       Date:  2009-07-24       Impact factor: 2.979

9.  Glatiramer acetate reduces the risk for experimental cerebral malaria: a pilot study.

Authors:  Peter Lackner; Andrea Part; Christoph Burger; Anelia Dietmann; Gregor Broessner; Raimund Helbok; Markus Reindl; Erich Schmutzhard; Ronny Beer
Journal:  Malar J       Date:  2009-02-27       Impact factor: 2.979

10.  The murine cerebral malaria phenomenon.

Authors:  Nicholas J White; Gareth D H Turner; Isabelle M Medana; Arjen M Dondorp; Nicholas P J Day
Journal:  Trends Parasitol       Date:  2009-11-22
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