Literature DB >> 16896119

Serum antibody levels to glycosylphosphatidylinositols in specimens derived from matched Malian children with severe or uncomplicated Plasmodium falciparum malaria and healthy controls.

Yacouba Cissoko1, Modibo Daou, Kirsten E Lyke, Alassane Dicko, Issa Diarra, Abdoulaye Kone, Ando Guindo, Karim Traore, Gowdahalli Krishnegowda, Dapa A Diallo, Ogobara K Doumbo, Christopher V Plowe, D Channe Gowda, Marcelo B Sztein.   

Abstract

Neutralizing antibodies to glycosylphosphatidylinositols (GPIs), which are Plasmodium falciparum surface protein anchor molecules implicated in malaria pathogenesis, are thought to protect against symptomatic malaria. Index cases of severe malaria in Malian children 3 months to 14 years of age were matched by age and residence to uncomplicated malaria and healthy controls. Serum antibodies to GPI (IgM and IgG) were measured at the time of severe malaria and after the malaria transmission season. The mean optical density values for IgM and IgG antibodies were higher in children with severe or uncomplicated malaria compared with healthy controls. Similarly, higher percentages of children with IgM and IgG antibodies to GPI were observed in the severe malaria group compared with matched healthy controls. IgG antibody levels to GPI were highest among children with cerebral malaria and children who died. The IgG antibody levels to GPI peaked during periods of malaria transmission and decreased after malaria transmission ended. A direct correlation between age and parasitemia and IgG antibodies to GPI was observed. In summary, higher levels of IgM and IgG antibodies to GPI in young children were associated with disease severity and were short-lived.

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Year:  2006        PMID: 16896119      PMCID: PMC2738947     

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  22 in total

1.  High-pH anion-exchange chromatography of glycoprotein-derived carbohydrates.

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Authors:  Kirsten E Lyke; Alassane Dicko; Abdoulaye Dabo; Lansana Sangare; Abdoulaye Kone; Drissa Coulibaly; Ando Guindo; Karim Traore; Modibo Daou; Issa Diarra; Marcelo B Sztein; Christopher V Plowe; Ogobara K Doumbo
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3.  Immunoglobulin G (IgG) responses to Plasmodium falciparum glycosylphosphatidylinositols are short-lived and predominantly of the IgG3 subclass.

Authors:  Craig S Boutlis; Peter K Fagan; D Channe Gowda; Moses Lagog; Charles S Mgone; Moses J Bockarie; Nicholas M Anstey
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Authors:  K E Lyke; R Burges; Y Cissoko; L Sangare; M Dao; I Diarra; A Kone; R Harley; C V Plowe; O K Doumbo; M B Sztein
Journal:  Infect Immun       Date:  2004-10       Impact factor: 3.441

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Authors:  Kirsten E Lyke; Alassane Dicko; Abdoulaye Kone; Drissa Coulibaly; Ando Guindo; Yacouba Cissoko; Karim Traoré; Christopher V Plowe; Ogobara K Doumbo
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Journal:  Am J Trop Med Hyg       Date:  2003-07       Impact factor: 2.345

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Journal:  J Immunol       Date:  1996-03-01       Impact factor: 5.422

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10.  Signal transduction in host cells by a glycosylphosphatidylinositol toxin of malaria parasites.

Authors:  L Schofield; F Hackett
Journal:  J Exp Med       Date:  1993-01-01       Impact factor: 14.307

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4.  Asymptomatic infection in individuals from the municipality of Barcelos (Brazilian Amazon) is not associated with the anti-Plasmodium falciparum glycosylphosphatidylinositol antibody response.

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5.  Inflammatory cytokine and humoral responses to Plasmodium falciparum glycosylphosphatidylinositols correlates with malaria immunity and pathogenesis.

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