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Parasite Immunol ; 39(1)2017 Jan.
Article in English | MEDLINE | ID: mdl-27741351

ABSTRACT

The role of T helper-17 (Th17) lymphocytes in the regulation of Schistosoma mansoni soluble egg antigen (SEA)-induced granuloma is unknown. This study examined the effect of Th17 cytokines (IL-17 and IL-22) on granulocyte recruitment and functions during SEA-induced granuloma formation in vitro in Schistosoma-infected and noninfected individuals. Granulocytes were isolated from 27 Schistosoma-infected patients and 13 controls and were used for granuloma induction using SEA-conjugated polyacrylamide beads in the presence of Th17 cytokines. Granuloma index was assessed, and granulocyte mediators such as tumour necrosis factor (TNF-α), hydrogen peroxide (H2 O2 ) and nitric oxide (NO) were measured in the culture supernatant at the 7th day using enzyme-linked immunosorbent assay (ELISA). Schistosoma-infected patients had significant larger SEA-induced granuloma than controls. IL-17 (125 pg/mL) induced the optimum size for granuloma within 3-7 days. However, IL-22 at different concentrations up to 300 pg/mL had no effect on granuloma formation. Using both cytokines simultaneously, IL-22 suppressed the effect of IL-17 and prevented granuloma formation. IL-17 significantly decreased TNF-α, H2 O2 and NO levels in Schistosoma-infected individuals. In contrast, IL-22 increased TNF-α and H2 O2 levels. In conclusion, IL-17 accelerates SEA-induced granuloma formation and inhibits granulocytes functions in Schistosoma-infected patients, while IL-22 inhibited the granuloma formation, but enhanced granulocyte functions.


Subject(s)
Granuloma/parasitology , Interleukin-17/immunology , Interleukins/immunology , Schistosoma mansoni/immunology , Schistosomiasis mansoni/immunology , Th17 Cells/immunology , Adult , Animals , Antigens, Helminth/immunology , Cytokines , Enzyme-Linked Immunosorbent Assay , Female , Granulocytes/immunology , Granuloma/immunology , Granuloma/pathology , Humans , Male , Mice , Middle Aged , Tumor Necrosis Factor-alpha , Interleukin-22
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