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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 32 (1990), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The capacity to induce complement-mediated cell lysis is greatly enhanced by truncating the hinge of IgG3 through exon deletions. This was shown by establishing five new cell lines which secreted chimeric IgG3 molecules with specificity for the hapten 4-hydroxy-3-nitrophenacetyl (NP) and having 47,45,32,15, and 0 amino acid hinge regions (the wild-type IgG3 has 62 amine acids in the hinge). Efficient complement activation and complement-mediated cell lysis did not depend on a long total hinge or on a long ‘upper’ hinge (the stretch From the beginning of the hinge to the first inter-heavy chain S-S bond).On the contrary, the mutant having a 15 amino acid hinge element was up to 10 times more efficient in complement lysis than the wild type. Thus the complement activation potential appeared to be down-regulated in the wild type. On the other hand, the mutant lacking the hinge altogether did not activate complement or induce complement-mediated cytolysis. These findings have to be taken into account when antibodies are designed for human therapy.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 39 (1994), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The Opsonophagocytic activity of the four human IgG subclasses was studied using chimeric mouse-human antibodies with specificity for the hapten NIP. As target cells we used haptenized sheep red blood cells and N. meningitidis, labelled with different amounts of hapten. We used polymorphonuclcar leucocytes (PMN) as effector cells to measure respiratory burst (RB), and U937 to measure phagocytosis/rosette formation. When the target cells were opsonized with antibody only, and PMN used as effector cells, lgG3 was highly efficient, while IgG1 revealed an intermediate activity and IgG2 and IgG4 were negative. The same pattern among the subclasses was obtained in the presence of complement source, when target cells with low hapten concentration were used. However, at high cpitope concentration on the target cells, in the presence of complement source, IgG2 was highly active. while IgG4 was still negative or only slightly positive. When U937 were used as effector cells and complement was omitted, IgG1, IgG3 and lgG4 all revealed high phagocylic/rosette-forming activity, while IgG2 was negative. When the target cells were opsonized with antibody and complement, the phagocytic/rosette-forming activity was often suppressed. Our results reveal that all four human IgG subclasses possess Opsonophagocytic capacity, but with different requirements concerning complement and Fc Rs. They also enlighten us as to how IgG2 might perform its protective effect against harmful bacteria displaying high density of carbohydrate epitopes on their outside surface.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 37 (1993), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The mammalian C-type serum lectin, mannan-binding protein (MBP), may induce Clq- and antibody-independent activation of the classical pathway of complement. Accordingly, MBP is considered as a member of the complement system. Complement deficiencies have been found with increased frequency in patients with meningococcal disease. Therefore, we investigated the MBP levels in patients with meningococcal disease. Ninety-nine Norwegian individuals (age 12–21 years) who survived severe systemic disease caused by serogroup B or C meningococci were investigated. No significant differences were observed in the MBP concentration between patients with serogroup B (n = 76) or C (n = 25) disease and healthy blood donor controls (n = 40) (P 〉0.05). The frequency of patients with low levels of MBP (〈 100 μg/1) was 10.1%. This was not different from controls (12.5%). Thus, low MBP concentrations do not appear to predispose to serogroup B or C meningococcal disease.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 31 (1990), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Subclasses of IgG antibodies to pneumococcal polysaccharide serotypc antigens 4, 6A. and 23F were measured before and 4 weeks after vaccination with pneumoeoccal vaccine in young individuals splencetomized because of trautna and in a control group. An ELISA technique was applied. IgG2 anti-pneuniococcal antibodies predominated before vaccination, especially against serotypes 4 anti 6A. The youngest individuals in the splenectomy group tended to have lower IgG2 antl-pneumococcal antibody levels than the older ones. Vaccination induced antibodies of the IgGl and IgG2 subclasses, and in sotne individuals also of the IgG4 subclass. Splencetomy does not seem to inffuence the IgG subcllass paltern of antipneuniococcal antibodies.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1619-7089
    Keywords: Antibody binding parameters ; Monodisperse polymer particles ; Radiolabelled monoclonal antibody fragments ; Surface-bound antigens
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The binding parameters of iodine-125-labelled intact monoclonal immunoglobulin G (IgG), F(ab′)2 and Fab′ fragments were compared. The study was carried out with the two monoclonal antibodies (MoAbs) K13 and K16 specific for human Ig light chains K and λ, respectively. When testing the 125I-MoAbs against monodisperse polymer particles coated with the specific antigens, the Ka for the F(ab′)2 fragments were similar to that for IgG, while the Ka for the Fab′ fragments were reduced to 10%–20% of that for IgG. The number N of effective target sites revealed with Fab′ was higher than with F(ab′)2 and IgG, presumably because less surface area is occupied by the small Fab′ molecules. The immunoreactive fraction F ranged according to IgG 〉 F(ab′)2 〉 Fab′. The explanation of the moderate difference between the Ka of the monoclonal Fab′ and the divalent IgG and F(ab′)2 was that the divalent molecules were not divalently attached to the particles. When testing the same antibody preparations against human lymphoma cells producing Ig with light chains K or λ, the binding results were less reliable than when particles were utilised, presumably due to antigen shedding. Different MoAbs vary in their loss of immunoreactivity due to enzymatic degradation and the radiolabelling procedure. The preparation of the radiolabelled fragments should therefore be optimized for each MoAb, and evaluation is necessary before injection. Artificial targets with a low leakage of antigen, like the monodisperse polymer particles here applied, are recommended for the in vitro evaluation of the immunoreactivity of labelled MoAb preparations.
    Type of Medium: Electronic Resource
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