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  • 1990-1994  (2)
  • Adhesion molecules  (1)
  • Complement receptors  (1)
  • 1
    ISSN: 1432-0533
    Keywords: Glioma ; Macrophages ; Microglia ; Fc-receptors ; Complement receptors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Cryostat sections of 12 gliomas and of 3 peritumoral brain tissue samples were investigated for mononuclear cell infiltration by immunohistochemistry, concentrating on cells expressing monocyte/macrophage markers. Only low numbers of T cells were detected in the tumors, whereas in average 20%–30% of all cells present in the samples were recognized by various macrophage markers. These cells carried surface epitopes with known function, like Fc-γ (Fcg) and complement receptors. Microglial cells, in comparison to typical debris laden macrophages, were only recognized by a restricted panel of macrophages markers (anti-Fcg receptors 1, 2, 3, complement receptor CR3, HLA DR, common leucocyte antigen CD45 and the monocyte marker RM3/1). In peritumoral tissue mainly dendritic, microglia-like cells were present, which revealed decreased expression of antigens CD4, RM3/1 and Fcg receptors in comparison to those in gliomas. A significant positive correlation was found between the number of RM3/1 or CR3 (CD11b)-positive cells and the proliferation rate of the tumors as documented by the number of bromodeoxyuridine-positive or Ki-67+ cells.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-4726
    Keywords: Mononuclear cells ; Adhesion molecules ; Cellular distribution ; Squamous cell carcinoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The expressions and cellular distributions of two pairs of adhesion molecules CD2/LFA-3 (leukocyte function-associated antigen-3) and LFA-1/ICAM-1 (intercellular adhesion molecule-1) were examined in inflammatory cellular infiltrates of advanced squamous cell carcinomas of the head and neck by immunohistochemical techniques including double-staining methods. Thirteen patients were investigated using the following monoclonal antibodies (mAbs): CD2, LFA-3 (CD58), ICAM-1 (CD54), LFA-1 (CD11a), the alpha/beta and gamma/delta T-cell receptor, pan T cells and broadly distributed monocyte/macrophage (m/mø) [Fc gamma RII (CD32), 25F9, RM3/1]. LFA-3 staining was observed on a high number of cells (968 ± 112 cells/mm2), correlating to the number of Fe gamma RII (CD32; P 〈 0.01), 25F9 (P 〈 0.05) and RM3/1 (P 〈 0.05) positive m/mø. Its ligand CD2 was found on 365 ± 126 cells/mm2, representing about 50% of CD3+ cells (730 ± 286 cells/mm2). CD2 positivity correlated to CD3 and CD8 (P 〈 0.01) but not to CD4+ T cells. LFA-1 and ICAM-1 were expressed on lymphocytes as well as on m/mø. ICAM-1+ cells (902 ± 205 cells/mm2) correlated to CD3+, CD8+ and RM3/1+ cells (P 〈 0.01). LFA-1 positivity (803 ± 255 cells/mm2) showed correlations to nearly all investigated antigens, as well as to CD4+ T cells (P 〈 0.05). These results show that different m/mø subsets display distinct patterns of adhesion molecule expressions suggesting different pathways of regulation. The CD3+ lymphocyte population revealed a lack of CD2 expression that was more pronounced in the CD4+ subset and indicated impaired lmyphocyte function.
    Type of Medium: Electronic Resource
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