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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 33 (1991), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The expression of leucocyte function-associated antigen 1 (LFA-1) was studied by immunofluorescence method on human peripheral blood mononuclear cells (PBMC) stimulated by the phytohaemagglutinin lectin (PHA).Monoclonal antibodies (MoAb) Mas 191c. IOT18 (directed against the β-chain. 95 kDa. CDI8) and IOT16. SPVL7, MHM24 (identificating the α-chain. 180 kDa, CD11a) were used, defining the CD 11a/ CD18' antibody panel.By means of cross-linking or competitive experiments, we showed that these antibodies recognized al least four distinct and spatially distant domains on the LFA-t molecule.Immunofluorescence analysis revealed that the up-regulation of LFA-1 expression was a late event, similar to the expression kinetics of the HLA DR and CD38 molecules, and followed the appearance of 0025 and CD71 molecules. Moreover, it was established that the LFA-1 up-regulation required mRNA and protein synthesis.Functional activity comparison of the different anti LFA-1 MoAb showed that the CDI la MoAb significantly inhibited the proliferation of lymphocytes stimulated by the phytohaemagglutinin lo various extents, as the LFA- 1α determinant identified, By contrast, the CD 18 MoAb did not influence strongly this cell process. We observed only n dim inhibitory effect with the CD18 MoAb recognizing an epitope common or very close to an LFA-1 α determinant.These results suggested that the LFA-1 antigen was important, at a molecular level, in the regulation of T-cell activation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 61 (1990), S. 271-277 
    ISSN: 1432-0584
    Keywords: Bone marrow ; Flow cytometry ; Monoclonal antibodies ; Hematopoiesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Bone marrow aspirates from 48 healthy donors (34 adults, 14 children) were analyzed by flow cytometry (FACS Analyzer) after purification of low-density bone marrow cells (Ld BMC) on a density gradient (d = 1,077) and labelling with 23 anti-hematopoietic cell monoclonal antibodies. Based on physical properties, these Ld BMC could be divided into four different populations called E, My, Mo and L, which comprised 14% ± 9%, 31% ± 16%, 10% ± 5% and 45% ± 14% of these cells, respectively. The phenotypic analysis of these different populations enabled the identification in E, of erythrocytes (Glycophorin A+, Rhesus D+, but negative for early erythroid differentiation markers such as the transferrin receptor (Tf. R) and the FA6-152 antigen); in My of cells of the myeloid lineage (VIM2+, HLA DR−); in Mo of cells of the monocytic lineage (VIM2+, CD14+) plus some myeloblasts (VIM2+, CD14−, HLADR+) and finally in L of a heterogeneous population including: 1. T lymphocytes labelled to the same extent by CD2, CD3, CD5 and CD6 (28% ± 10%), B lymphocytes assessed by CD19 and CD20 (12% ± 8%), Pre-B cells (CD10+ = 8% ± 7%), less than 5% of “natural killer” cells (CD16+ or Leu7+) and finally, less than 6% of myelomonocytes (CD14+ and/or VIM2+). 2. The erythroid lineage (rhesus D+ = 42% ± 20%, Tf.R+ and FA6-152+ = 32% ± 12%). 3. Undifferentiated cells or progenitor cells (CD34+ = 7% ± 5%). 4. Cells unlabelled by any antibodies (approximately 6%). We observed no difference between bone marrow samples from adults or children, with respect to physical properties, and with all but four immunological markers. A significantly higher proportion of B cells (CD19+ and CD10+) (P〈0.001) and undifferentiated cells (CD34+ and HLADR+) (P〈0.02) was observed in children. These data, obtained from a large number of bone marrow samples, could be used to quantify the imbalance of some bone marrow disorders.
    Type of Medium: Electronic Resource
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