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dc.contributor.authorMoormann, Ann M.
dc.contributor.authorSumba, Peter Odada
dc.contributor.authorTisch, Daniel J.
dc.contributor.authorEmbury, Paula E.
dc.contributor.authorKing, Charles H.
dc.contributor.authorKazura, James W.
dc.contributor.authorJohn, Chandy C.
dc.date2022-08-11T08:10:40.000
dc.date.accessioned2022-08-23T17:15:54Z
dc.date.available2022-08-23T17:15:54Z
dc.date.issued2009-08-27
dc.date.submitted2010-06-08
dc.identifier.citationAm J Trop Med Hyg. 2009 Sep;81(3):489-95. <a href="http://www.ajtmh.org/cgi/reprint/81/3/489">Link to article on publisher's site</a>
dc.identifier.issn0002-9637 (Linking)
dc.identifier.pmid19706920
dc.identifier.urihttp://hdl.handle.net/20.500.14038/47271
dc.description.abstractLong-term planning to prevent malaria epidemics requires in-depth understanding of immunity to Plasmodium falciparum in areas of unstable transmission. Cytokine responses to immunodominant epitope peptides from liver stage antigen 1 (LSA-1) and thrombospondin-related adhesive protein (TRAP) were evaluated over a nine-month interval in adults and children in Kenya from a malaria epidemic-prone highland area after several years of low transmission. The proportion and magnitude of interferon-gamma ELISPOT responses and the proportion of interleukin-10 responders to LSA-1 and TRAP peptides tended to be higher in adults than children. Frequencies of interferon-gamma responders to these peptides were similar at the two time points, but responses were not consistently generated by the same persons. These results suggest that T cell memory to pre-erythrocytic stage malaria antigens is maintained but may be unavailable for consistent detection in peripheral blood, and that these antigens induce both pro-inflammatory and anti-inflammatory cytokine responses in this population.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=19706920&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ajtmh.org/cgi/reprint/81/3/489
dc.subjectAdolescent
dc.subjectAdult
dc.subjectAnimals
dc.subjectAntigens, Protozoan
dc.subjectCells, Cultured
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectGene Expression Regulation
dc.subjectHumans
dc.subjectImmunodominant Epitopes
dc.subjectInterferon-gamma
dc.subjectInterleukin-10
dc.subjectKenya
dc.subjectLeukocytes, Mononuclear
dc.subjectMalaria, Falciparum
dc.subjectParasitemia
dc.subjectPlasmodium falciparum
dc.subjectPrevalence
dc.subjectProtozoan Proteins
dc.subjectTime Factors
dc.subjectYoung Adult
dc.subjectBiostatistics
dc.subjectEpidemiology
dc.subjectHealth Services Research
dc.subjectImmunology and Infectious Disease
dc.subjectPediatrics
dc.titleStability of interferon-gamma and interleukin-10 responses to Plasmodium falciparum liver stage antigen 1 and thrombospondin-related adhesive protein immunodominant epitopes in a highland population from Western Kenya
dc.typeJournal Article
dc.source.journaltitleThe American journal of tropical medicine and hygiene
dc.source.volume81
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/qhs_pp/411
dc.identifier.contextkey1347942
html.description.abstract<p>Long-term planning to prevent malaria epidemics requires in-depth understanding of immunity to Plasmodium falciparum in areas of unstable transmission. Cytokine responses to immunodominant epitope peptides from liver stage antigen 1 (LSA-1) and thrombospondin-related adhesive protein (TRAP) were evaluated over a nine-month interval in adults and children in Kenya from a malaria epidemic-prone highland area after several years of low transmission. The proportion and magnitude of interferon-gamma ELISPOT responses and the proportion of interleukin-10 responders to LSA-1 and TRAP peptides tended to be higher in adults than children. Frequencies of interferon-gamma responders to these peptides were similar at the two time points, but responses were not consistently generated by the same persons. These results suggest that T cell memory to pre-erythrocytic stage malaria antigens is maintained but may be unavailable for consistent detection in peripheral blood, and that these antigens induce both pro-inflammatory and anti-inflammatory cytokine responses in this population.</p>
dc.identifier.submissionpathqhs_pp/411
dc.contributor.departmentDepartment of Pediatrics
dc.contributor.departmentDepartment of Quantitative Health Sciences
dc.source.pages489-95


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