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    Gamma interferon responses to Plasmodium falciparum liver-stage antigen 1 and thrombospondin-related adhesive protein and their relationship to age, transmission intensity, and protection against malaria

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    Authors
    John, Chandy C.
    Moormann, Ann M.
    Sumba, Peter Odada
    Ofulla, Ayub V.
    Pregibon, Daniel C.
    Kazura, James W.
    UMass Chan Affiliations
    Department of Pediatrics
    Department of Quantitative Health Sciences
    Document Type
    Journal Article
    Publication Date
    2004-08-24
    Keywords
    Adolescent
    Adult
    Aging
    Animals
    Antigens, Protozoan
    Child
    Child, Preschool
    Enzyme-Linked Immunosorbent Assay
    Humans
    Interferon-gamma
    Kenya
    Malaria, Falciparum
    Plasmodium falciparum
    Protozoan Proteins
    Biostatistics
    Epidemiology
    Health Services Research
    Immunology and Infectious Disease
    Pediatrics
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    Link to Full Text
    http://dx.doi.org/10.1128/IAI.72.9.5135-5142.2004
    Abstract
    Gamma interferon (IFN-gamma) responses to the Plasmodium falciparum antigens liver-stage antigen 1 (LSA-1) and thrombospondin-related adhesive protein (TRAP) are thought to be important in protection against malaria. Optimal methods of testing and the effects of age and transmission intensity on these responses are unknown. IFN-gamma responses to LSA-1 and TRAP peptides were assessed by the enzyme-linked immunospot assay (ELISPOT) and enzyme-linked immunosorbent assay (ELISA) in children and adults from areas of stable and unstable malaria transmission in Kenya. Adults in the areas of stable and unstable transmission had similar frequencies and levels of IFN-gamma responses to LSA-1 and TRAP as determined by ELISPOT and ELISA. In contrast, IFN-gamma responses to the LSA-1 T3 peptide (assessed by ELISPOT) and to any LSA-1 peptide (assessed by ELISA) were less frequent in children in the area of unstable transmission than in children in the area of stable transmission. IFN-gamma responses to LSA-1 were more frequently detected by ELISA than by ELISPOT in the stable-transmission area. IFN-gamma responses detected by ELISA and ELISPOT did not correlate with each other. In children in the stable-transmission area, IFN-gamma responses to LSA-1 peptides assessed by ELISA, but not by ELISPOT, were associated with protection against clinical malaria and anemia. IFN-gamma responses to LSA-1 appear to require repeated P. falciparum exposure and/or increased age and, as measured by ELISA, are associated with protection against clinical malaria and anemia.
    Source
    Infect Immun. 2004 Sep;72(9):5135-42. Link to article on publisher's site
    DOI
    10.1128/IAI.72.9.5135-5142.2004
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/47245
    PubMed ID
    15322007
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1128/IAI.72.9.5135-5142.2004
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    Population and Quantitative Health Sciences Publications

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