Please use this identifier to cite or link to this item: https://hdl.handle.net/10646/2730
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dc.contributor.authorNausch, Norman-
dc.contributor.authorMidzi, Nicholas-
dc.contributor.authorMduluza, Takafira-
dc.contributor.authorMaizels, Rick M.-
dc.contributor.authorMutsaka, Francisca-
dc.date.accessioned2016-07-11T08:29:11Z-
dc.date.available2016-07-11T08:29:11Z-
dc.date.issued2011-02-10-
dc.identifier.citationNausch N, Midzi N, Mduluza T, Maizels RM, Mutapi F (2011) Regulatory and Activated T Cells in Human Schistosoma haematobium Infections. PLoS ONE 6(2): e16860. doi:10.1371/journal.pone.0016860en_US
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/10646/2730-
dc.description.abstractAcquired immunity against helminths is characterised by a complex interplay between the effector Th1 and Th2 immune responses and it slowly manifests with age as a result of cumulative exposure to parasite antigens. Data from experimental models suggest that immunity is also influenced by regulatory T cells (Treg), but as yet studies on Treg in human schistosome infections are limited. This study investigated the relationship between schistosome infection intensity and the two cell populations regulatory T cells (Treg: CD4+(dim)CD25+(high)FOXP3+CD127low), and activated (Tact: CD4+CD25+FOXP32) T cells in Zimbabweans exposed to Schistosoma haematobium parasites. Participants were partitioned into two age groups, young children (8–13 years) in whom schistosome infection levels were rising to peak and older people (14+ years) with declining infection levels. The relationship between Tact proportions and schistosome infection intensity remained unchanged with age. However, Treg proportions rose significantly with increasing infection in the younger age group. In contrast Treg were negatively correlated to infection intensity in the older age group. The relative proportions of regulatory T cells differ significantly between young individuals in whom high infection is associated with an enhanced regulatory phenotype and older infected patients in whom the regulatory response is attenuated. This may influence or reflect different stages of the development of protective schistosome acquired immunity and immunopathogenesis.en_US
dc.description.sponsorshipWellcome Trust UK (Grant no WT082028MA), http://www.wellcome.ac.uk/; Medical Research Council UK (Grant no G81/538), www.mrc.ac.uk; Cunningham Trust; and Carnegie Trust for the Universities of Scotland, http://www.carnegie-trust.org/.en_US
dc.language.isoen_ZWen_US
dc.publisherPLoS Oneen_US
dc.subjecthelminthsen_US
dc.subjectparasite antigensen_US
dc.subjectT cellsen_US
dc.subjecthuman schistosome infectionsen_US
dc.subjectTact proportionsen_US
dc.subjectSchistosoma haematobiumen_US
dc.subjectimmunopathogenesisen_US
dc.titleRegulatory and Activated T cells in human schistosoma haematobium infectionsen_US
dc.typeArticleen_US
dc.contributor.authoremailnnausch@staffmail.ed.ac.uken_US
Appears in Collections:Biochemistry Staff Publications

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