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  • 1
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Investigations based on computer simulated distributions of histamine in blood plasma were recently devoted to the assessment of the roles of cysteine, aspartic and glutamic acids as possible adjuvants of zinc to favour histamine tissue diffusion through mixed-ligand coordination. Since all tissues contain at least one of the two enzymes required for the catabolism of histamine, any increase of its tissue diffusion is expected to result in an acceleration of its degradation, which may be of interest for the treatment of anaphylactic disorders. As an extension of these studies, the present paper first reports (i) an experimental investigation of the tendency of four dicarboxylic acids, namely malate, malonate, tartrate and maleate, to mixed-ligand coordination with zinc and histamine, (ii) computer-based potential effects to be expected from the association of these agents to zinc with respect to histamine tissue diffusion. Cell culture studies were then used to test simulation expectations. Two series of experiments involving successively human lymphocytes and a lymphoblastoid cell line (8866) have been carried out, which led to the following conclusions: (i) the hypothesis formerly put forward that cysteine could favour histamine tissue diffusion through mixed-ligand coordination with zinc has been validated on the two cell models, (ii) the formerly established suppressive role of histamine versus lymphocyte proliferation has clearly been confirmed, (iii) moreover, this suppressive effect has been shown to occur correlatively to histamine uptake by these cells, (iv) the four dicarboxylic acids, more especially tartric acid, proved effective as catalysts of the two above processes. Possible biomedical applications of these results are discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Veterinary Immunology and Immunopathology 39 (1993), S. 365-379 
    ISSN: 0165-2427
    Keywords: [abr] ANA; antinuclear antibody ; [abr] ARA; American Rheumatism Association ; [abr] Ag; antigen ; [abr] CIC; circulating immune complexes ; [abr] OD; optical density ; [abr] RA; rheumatoid arthritis ; [abr] RF; rheumatoid factor ; [abr] RIA; radio immunoassay ; [abr] ULN; upper limit of normal
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1574-695X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: Abstract The peripheral blood mononuclear cells (PBMC) of woodchucks experimentally infected by woodchuck hepatitis virus (WHV) were examined simultaneously for the presence of membrane associated WHV antigens by cytofluorometry, and for WHV DNA and RNA sequences by the polymerase chain reaction (PCR). Four woodchucks were inoculated: two with a well-defined infectious inoculum and two with an inoculum obtained from an animal at the late incubation phase, which was positive for WHV DNA by PCR but still devoid of WHV markers. Infection was demonstrated in all four inoculated woodchucks by the appearance at different times of WHV DNA and WHV antigens in both leucocytes and serum. WHV DNA was first detected by PCR either in the serum (two cases) or in leucocytes (two cases). The mean percentage of cells positive for membrane associated WHsAg or WHcAg detected by cytofluorometry were 37%±25 and 17%±15 respectively. After 8 weeks, all inoculated animals were WHsAg positive in serum. These data suggest that PBMC are involved in the early events of hepadnavirus infection. They also show that sera which are positive by PCR for WHV DNA may transmit viral infection even while still seronegative for WHV markers and for WHV DNA by dot blot.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: After binding lo the CD4 receptor, the human Immunodeficiency virus I HIV-I)may enter the T cell and induce the formation of multinucleated giant cells (syncytia). As well as the CD4 molecule, other molecules, such as the lymphocyte function-associated antigen 1(LFA-1. CD11a/CD 18) have been shown to be involved in HIV-l-mediated cell fusion.This study was designed to define regions on the human CD1la/CD18 molecule important for the HIV-l-induced syncytium formation A CD11a/CD18 MoAb panel discriminating at least five distinct and spatially distant domains of the LFA-l molecule was used. Comparison of the functional activity of different MoAbs demonstrated that all epitopes of the LFA-1 molecule were not of equal importance m HIV-1-induced syncytium formation between H9.III cells chronically infected with HIV-1 and uninlecledCD4+ Sup T1 cells. We also demonstrated that CD11a/CD18 MoAbs inhibit syncytia formation only at the level of the uninfected Sup T1 cells, suggesting that the LPA-1 molecule expressed on Sup T1 ceils interacts with ligand(s) expressed on the infected H9. III cells. Two potential LFA-1 receptors on the H9.III cells were tested: t he ICAM-1 molecule (intercellular adhesion molecule 1.CD54)and the HIV-1 transmembrance glycoprotein41 (gp4l), A CD54 MoAb (84H10) partially inhibited syncytia formation, thus demonstrating the involvement of the ICAM-1 molecule in the HIV-l-mediated cell fusion. However, the CD11a/CD18 MoAbs do not inhibit binding of the viral envelope glycoprotein gp41 to the cell surface, irrespective of the MoAb concentration used.Although we have not been successful in identifying all candidate fusion receptors for the LFA-1 molecule, these data suggest that some LFA.-1 regions are important for syncytium formation and. therefore, in the cell-to-cell transmission of virus and in the spread of infection.
    Type of Medium: Electronic Resource
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  • 5
    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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  • 6
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    Unknown
    Paris : Periodicals Archive Online (PAO)
    Etudes anglaises. 40:2 (1987:avril/juin) 238 
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  • 7
    facet.materialart.
    Unknown
    Paris : Periodicals Archive Online (PAO)
    Etudes anglaises. 40:2 (1987:avril/juin) 238 
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  • 8
    ISSN: 1432-0711
    Keywords: Alloimmunization ; Haemolytic disease ; Newborn
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary During the last thirty years, the diagnosis, management and prevention of haemolytic disease of the newborn infant (HDN) have improved. From 1959 to 1988, 3004 HDN (ABO excluded) have been collected. The percentage of HDN with anti-D alloimmunization decreased significantly (98.4% from 1959 to 1968, 93.5% from 1969 to 1978 and 68.1% from 1979 to 1988). The anti-D HDN with exchange transfusion (ET) fell significantly between the first and second periods (577 versus 970;X 2=19.92;P〈0.001). On the other hand, the number of HDN other than anti-D increased during these three periods, but the percentage of these HDN which needed ET decreased. Our study shows the long term efficiency of the prevention of anti-D alloimmunization (since 1970) and of the irregular antibodies screening among all pregnant women (since 1979).
    Type of Medium: Electronic Resource
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  • 9
    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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