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pubmed-article:10070666pubmed:abstractTextThe cellular inflammatory response in the small intestine of 21 goats infected with Schistosoma bovis was phenotypically characterized by immunohistochemistry between 6 and 32 weeks post-exposure, with particular reference to perioval granulomatous reactions. Macrophages of granulomas consistently expressed MHC class II molecules, whereas multi-nucleated giant cells in general did not. Most granulomas contained moderate infiltrates of CD2+ (CD4+ or CD8+) and gamma/delta (T19+) T cells, whereas B lymphocytes were sparse. Intact extravascular mucosal eggs, lacking appreciable cellular reactivity on plain histopathology, displayed surrounding collars of MHC class II+ macrophages. Gamma/delta T cells and MHC class II+ macrophages were the predominant cell types in perivascular inflammatory cell clusters in the submucosa. The phenotypic cellular composition of granulomas did not change appreciably with duration of infection. The results indicate the importance of MHC class II-restricted immune events in the caprine S. bovis egg granulomas and also suggest a role of gamma/delta T cells in their pathogenesis. It is hypothesized that the early appearance of perioval macrophage collars may serve to protect eggs from ovicidal host defence mechanisms, facilitating excretion and continuation of the life-cycle.lld:pubmed
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pubmed-article:10070666pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10070666pubmed:articleTitleAn immunohistological study of phenotypic characteristics of cells of the inflammatory response in the intestine of Schistosoma bovis-infected goats.lld:pubmed
pubmed-article:10070666pubmed:affiliationDepartment of Pathology, Faculty of Veterinary Medicine, Swedish University of Agricultural Sciences, Uppsala, Sweden. Ronny.Lindberg@pat.slu.selld:pubmed
pubmed-article:10070666pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10070666pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:10070666pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed