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15 September 2006

Volume 194, Number 6
The Journal of Infectious Diseases 2006;194:837–845
0022-1899/2006/19406-0017$15.00
DOI: 10.1086/506623
MAJOR ARTICLE

Low Levels of RANTES Are Associated with Mortality in Children with Cerebral Malaria

Chandy C. John,1

Robert Opika‐Opoka,2

Justus Byarugaba,2

Richard Idro,2 and

Michael J. Boivin3

1University of Minnesota Medical School, Minneapolis; 2Michigan State University, Lansing; 3Makerere University Faculty of Medicine, Kampala, Uganda

Background.In children with cerebral malaria (CM), serum chemokine levels and associated morbidity and mortality have not been characterized.

Methods.Serum levels of the cytokines interleukin (IL)–1β, IL‐6, IL‐10, interferon (IFN)–γ, and tumor necrosis factor–α and the chemokines macrophage inflammatory protein (MIP)–1α, MIP‐1β, and regulated upon activation, normal T cell expressed and secreted (RANTES) were measured in Ugandan children with CM, in children with uncomplicated malaria (UM), and in healthy children from the community, as control subjects (CCs).

Results.Children with CM had lower levels of RANTES and higher levels of all other cytokines and chemokines than CCs (all ), and they had lower levels of RANTES ( ) and higher levels of IL‐10 ( ), IFN‐γ ( ), and IL‐1β ( ) than children with UM. Children with CM who died had lower levels of RANTES ( ) and higher of levels of IL‐6 ( ), IL‐10 ( ), IFN‐γ ( ), and MIP‐1β ( ) than children who survived. After adjustment for other cytokine and chemokine levels, only low levels of RANTES were independently associated with mortality ( ). Levels of RANTES correlated with platelet count but were associated with mortality independently of platelet count.

Conclusions.The serum cytokine and chemokine profile of children who die of CM is similar to that of individuals who die of sepsis. Levels of RANTES are significantly lower in children with CM, and very low levels of RANTES are associated with mortality, independently of other cytokine and chemokine levels.

Received 24 March 2006; accepted 2 May 2006; electronically published 16 August 2006.

Reprints or correspondence: Dr. Chandy C. John, University of Minnesota, Dept. of Pediatrics, 420 Delaware St. SE, 850 Mayo, MMC‐296, Minneapolis, MN 55455 ().

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Online publication date: 1-Jul-2009.
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Collins Ouma, Gregory C. Davenport, Gordon A. Awandare, Christopher C. Keller, Tom Were, Michael F. Otieno, John M. Vulule, Jeremy Martinson, John M. Ong’echa, Robert E. Ferrell, and Douglas J. Perkins. (2008) Polymorphic Variability in the Interleukin (IL)–1β Promoter Conditions Susceptibility to Severe Malarial Anemia and Functional Changes in IL‐1β Production. The Journal of Infectious Diseases 198:8, 1219-1226
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Jean Langhorne, Francis M Ndungu, Anne-Marit Sponaas, Kevin Marsh. (2008) Immunity to malaria: more questions than answers. Nature Immunology 9:7, 725-732
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J. LELLO, T. HUSSELL. (2008) Functional group/guild modelling of inter-specific pathogen interactions: A potential tool for predicting the consequences of co-infection. Parasitology 135:07,
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Online publication date: 25-Apr-2008.
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Bernard N Kanoi, Thomas G Egwang. (2007) New concepts in vaccine development in malaria. Current Opinion in Infectious Diseases 20:3, 311???316
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  • Potential conflicts of interest: none reported.

    Financial support: National Institutes of Health (Fogarty Institute grant R21 TW‐006794 to C.C.J.); Institute of International Education (Fulbright African Regional Research Award to M.J.B.).

    This work was conducted while C.C.J. was at Case Western Reserve University and M.J.B. was at Indiana Wesleyan University.

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