Proportions of CD41 memory T cells are altered in individuals chronically infected with Schistosoma haematobium

نویسندگان

  • Norman Nausch
  • Claire D. Bourke
  • Laura J. Appleby
  • Nadine Rujeni
  • Olivier Lantz
  • François Trottein
  • Nicholas Midzi
  • Takafira Mduluza
  • Francisca Mutapi
چکیده

Institute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, Ashworth Laboratories, King’s Buildings, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, UK, Laboratoire d’Immunologie, et Unité Inserm 932, InsermCIC-BT507 IGR/Curie, Institut Curie, 75005 Paris, France, Center for Infection and Immunity of Lille, INSERM U 1019, CNRS UMR 8204, Univ Lille Nord de France, Institut Pasteur de Lille, 1, rue du Professeur Calmette, 59019 Lille Cedex, France, National Institute of Health Research, PO Box CY 573, Causeway, Harare, Zimbabwe, Department of Biochemistry, University of Zimbabwe, PO Box 167, Mount Pleasant, Harare, Zimbabwe.

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Proportions of CD4+ memory T cells are altered in individuals chronically infected with Schistosoma haematobium

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Age-Related Patterns in Human Myeloid Dendritic Cell Populations in People Exposed to Schistosoma haematobium Infection

BACKGROUND Urogenital schistosomiasis is caused by the helminth parasite Schistosoma haematobium. In high transmission areas, children acquire schistosome infection early in life with infection levels peaking in early childhood and subsequently declining in late childhood. This age-related infection profile is thought to result from the gradual development of protective acquired immunity. Age-r...

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Regulatory and Activated T Cells in Human Schistosoma haematobium Infections

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 stu...

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T cell clones from Schistosoma haematobium infected and exposed individuals lacking distinct cytokine profiles for Th1/Th2 polarisation.

T cell clones were derived from peripheral blood mononuclear cells of Schistosoma haematobium infected and uninfected individuals living in an endemic area. The clones were stimulated with S. haematobium worm and egg antigens and purified protein derivative. Attempts were made to classify the T cell clones according to production of the cytokines IL-4, IL-5 and IFN-gamma. All the T cell clones ...

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T-helper 17 cells are associated with pathology in human schistosomiasis.

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تاریخ انتشار 2012