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Vet Pathol ; 49(5): 784-95, 2012 Sep.
Article in English | MEDLINE | ID: mdl-21987303

ABSTRACT

Meningiomas are the most common intracranial tumors in dogs. A variety of inflammatory cells have been shown to invade these tumors in people, but little is known about interactions between the immune system and naturally occurring brain tumors in dogs. The purpose of this study was to investigate the presence of a variety of immune cell subsets within canine intracranial meningiomas. Twenty-three formalin-fixed, paraffin-embedded tumor samples were evaluated using immunohistochemistry with antibodies specific for CD3, CD79a, CD18, CD11d (αD), CD45RA, forkhead box P3, and Toll-like receptors 4 and 9. Immune cell infiltration was evident in all samples, with a predominance of CD3(+) T cells. Large numbers of CD18(+) microglia and macrophages were noted surrounding and infiltrating the tumors, and a subset of these cells within the tumor appeared to be CD11d(+). Scattered macrophages at the tumor-brain interface were TLR4(+) and TLR9(+). Rare CD79a(+) B cells were noted in only a small subset of tumors. Lesser numbers of lymphocytes that were CD11d(+), CD45RA(+), or FoxP3(+) were noted in a number of the meningiomas. Although the function of these cells is not yet clear, work in other species suggests that evaluation of this immune cell infiltrate may provide important prognostic information and may be useful in the design of novel therapies.


Subject(s)
Dog Diseases/immunology , Lymphocyte Subsets/immunology , Lymphocytes, Tumor-Infiltrating/immunology , Macrophages/immunology , Meningeal Neoplasms/veterinary , Meningioma/veterinary , Animals , Antigens, CD/analysis , Antigens, CD/immunology , Biomarkers, Tumor/metabolism , Cytokines/metabolism , Dog Diseases/pathology , Dogs , Female , Forkhead Transcription Factors/metabolism , Immunohistochemistry/veterinary , Male , Meningeal Neoplasms/immunology , Meningeal Neoplasms/pathology , Meningioma/immunology , Meningioma/pathology , Paraffin Embedding/veterinary , Toll-Like Receptor 4/metabolism , Toll-Like Receptor 9/metabolism
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