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  • 1
    ISSN: 1573-7373
    Keywords: glioma ; tumor-associated antigen ; immunohistochemistry ; monoclonal antibody ; IgM
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The present study was undertaken to determine thepattern of immunoreactivity of BT32/A6, a human IgMmonoclonal antibody (MAb), with the following histological panels:1) 30 human and non-human cell lines, 2)32 normal human tissues, and 3) 28 tumorsof central neuroepithelial origin (16 astrocytic; 11 non-astro-cytic).Antibody BT32/A6 recognizes a surface and cytoplasmic antigenpresent on a variety of human tumor celllines including gliomas, melanomas, neuroblastomas, and a fewsarcomas. The antigen is present (at least focally)on 15/16 astrocytic tumor tissue sections (94%), andin some cases, on close to 100% ofcells. All malignant cell types, including small anaplasticcells, giant cells, gemistocytic cells, and cells formingpseudopalisades were labeled by MAb BT32/A6. Non-astrocytic neuroepithelialtumors did not stain appreciably with MAb BT32/A6.There was weak immunoreactivity in a small subsetof normal human tissues of epithelial and lymphoidorigin, with the exception of adrenal cortex, whichexhibited weak to moderate staining. All normal tissuesof neuroectodermal and mesenchymal origin were unreactive. Inconclusion, MAb BT32/A6 appears to be unique inthat it recognizes a highly-expressed astrocytic tumor-associated antigenthat is present on both low and highgrade tumors. This makes it a strong candidatefor further studies aimed at establishing its usefulnessin the treatment of human astrocytic tumors.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-0832
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The role of humoral antibodies and the effect of BCG vaccination were studied in the experimental candidiasis in mice. The antibody suppressed, B-cell deficient animals were prepared by repeated administration of rabbit anti-mouse-μ-antiserum to the new born mice from birth onwards. Such immunodeficient animals along with controls were infected intravenously with Candida albicans, to study the course of candidal infection. It was observed that B-cell-deficient animals were found to be more susceptible to candidal infection than the controls, as indicated by their steady loss of body weight, longer mean time to death and higher viable counts of candidal cells in different organs. The anti-candidal antibodies were absent in all B-cell-deficient animals but present in the controls. These results suggest that antibodies make a contribution in protection against candidal infection in mice. The BCG vaccinated animals were prepared by repeated intravenous administration of BCG to mice and these vaccinated animals along with unvaccinated controls were challenged intravenously with C. albicans, to study the course of candidal infection. It was observed that BCG vaccination prolonged meantime to death and reduced the number of candidal cells in their kidneys.
    Type of Medium: Electronic Resource
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