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    Regulatory and Activated T cells in human schistosoma haematobium infections

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    Nausch_et_al_Regulatory_and_activated_T_cells_in_human_schistosoma.pdf (443.0Kb)
    Date
    2011-02-10
    Author
    Nausch, Norman
    Midzi, Nicholas
    Mduluza, Takafira
    Maizels, Rick M.
    Mutsaka, Francisca
    Type
    Article
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    Abstract
    Acquired 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.
    URI
    http://hdl.handle.net/10646/2730
    Additional Citation Information
    Nausch 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.0016860
    Sponsor
    Wellcome 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/.
    Publisher
    PLoS One
    Subject
    helminths
    parasite antigens
    T cells
    human schistosome infections
    Tact proportions
    Schistosoma haematobium
    immunopathogenesis
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    • Biochemistry Staff Publications [10]

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