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Murine Monoclonal Antibody (murine + monoclonal_antibody)
Selected AbstractsORIGINAL ARTICLE: Murine Monoclonal Antibody 26 Raised Against Tetanus Toxoid Cross-Reacts with ,2 -Glycoprotein I: Its Characteristics and Role in Molecular MimicryAMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, Issue 1 2009Aleksandra Inic-Kanada Problem, Studies on experimental antiphospholipid syndrome (APS) models proved that molecular mimicry between plasma protein ,2 -glycoprotein I (,2GPI) and structure within micro-organisms or their products, might be a cause for experimental APS. Considering the heterogeneity of polyclonal antiphospholipid antibodies (aPLs), it is important to define the precise characteristics of pathogenic aPLs. To avoid the influence of polyclonality and to further analyse the connection between molecular mimicry and APS, we produced monoclonal antibodies (MAbs) against tetanus toxoid (TTd) and tested their reactivity against ,2GPI. Method of study, In this report, we analysed the characteristics of MAb26 raised against TTd and cross-reactive with ,2GPI: its binding properties in various in vitro immunoassays, its specific interactions with surface epitopes expressed on apoptotic cells and its role in vivo. Results, We have demonstrated that MAb26: (i) binds ,2GPI being immobilized on an appropriate surface: irradiated polystyrene plates, non-irradiated plates pre-coated with anionic phospholipids and polyvinylidene fluoride membrane; (ii) binds specifically to apoptotic but not to viable cells and the binding is ,2GPI-dependent; and (iii) induces a pathologic pregnancy outcome when passively injected into BALB/c mice. Conclusion, This study concluded that certain subpopulations of antibodies raised against TTd and cross-reactive with ,2GPI, because of the molecular mimicry mechanism, could have pathologic potential. [source] Neovascularization and mast cells with tryptase activity increase simultaneously in human pterygiumJOURNAL OF CELLULAR AND MOLECULAR MEDICINE, Issue 3 2007Domenico Ribatti Abstract Mast cells (MC) have been implicated in both normal and pathological angiogenesis, such as that in chronic inflammatory diseases and tumors. This assumption is partially supported by the close structural association between MC and blood vessels and the recruitment of these cells during tumor growth. MC release a number of angiogenic factors among which tryptase, a serine protease stored in MC granules, is one of the most active. In this study, we correlate the extent of angiogenesis with the number of tryptase-reactive MC in tissue fragments from pterygium and normal bulbar conjunctiva investigated by immunohistochemistry, using two murine monoclonal antibodies against the endothelial cell marker CD31 and the MC marker tryptase. Angiogenesis, measured as microvessel density, was highly correlated with MC tryptase-positive cell count in pterygium tissues. These results suggest that the characteristic neovascularization observed in pterygium may be sustained, at least in part, by MC angiogenic mediators, in particular tryptase. [source] A novel monoclonal antibody recognizing ,(1,3) glucans in intact cells of Candida and Cryptococcus,APMIS, Issue 10 2008N. KONDORI The cell walls of all medically important fungi contain a unique polyglucose compound, ,(1,3) glucan. In the present study, murine monoclonal antibodies were produced against linear and ,(1,6) branched ,(1,3) glucans, and their specificities were characterized for reactivity to other , glucans, fungal cell wall fragments, and fungal cells. Their reactivity was also compared with that of rabbit polyclonal antibodies raised against the same immunogens. Two mouse monoclonal antibodies (AG and BG) recognized immunoreactive epitopes in ,(1,3)(1,6) glucan by ELISA. In an inhibition assay of the anti-,(1,3)(1,6) activity of the monoclonals, the homologous antigen effectively inhibited the activity as expected, while ,(1,3) also inhibited the assay but to a much lesser extent. No inhibition was obtained by ,(1,3)(1,4) or ,(1,6), while a cell wall extract of Candida albicans (PPM) effectively inhibited both monoclonals. Cell wall fragments of C. albicans (CaCW) and Cryptococcus neoformans (CnCW) inhibited the anti-,(1,3)(1,6) activity of AG, while BG was much less or not inhibited at all. Immunofluorescence confirmed the unique antibody specificity of AG by its recognition of a ,(1,3)(1,6)-associated epitope on the cell surfaces of C. albicans,C. krusei, C. glabrata, and nonencapsulated C. neoformans. The epitope for the AG antibody is suggested to be present in the branching point of ,(1,3)(1,6), or in the randomly coiled ,(1,3) polyglucan due to the presence of branches. Thus, monoclonal antibodies to ,(1,3)(1,6) glucans may have potential as tools in the laboratory diagnosis of invasive yeast infections. [source] Monoclonal antibody of IgG isotype against a cross-reactive lipopolysaccharide epitope of Chlamydia and Salmonella Re chemotype enhances infectivity in L-929 fibroblast cellsFEMS IMMUNOLOGY & MEDICAL MICROBIOLOGY, Issue 2 2002Iana H. Haralambieva Abstract A murine monoclonal antibody (MAb) 202D7 of IgG3 isotype recognizes a lipopolysaccharide (LPS) epitope of Chlamydia spp. and cross-reacts with the Re chemotype LPS of Salmonella and Escherichia coli. The antibody exhibits strong complement activating properties and stimulates phagocytosis of Salmonella enterica serovar Minnesota Re mutant by murine macrophages. Salmonella Re mutants are non-invasive for cell monolayers but still can enter and replicate in L-929 murine fibroblast cells. The entry of bacteria within the cells increases five-fold in the presence of MAb 202D7. The antibody mediates attachment and enhances five-fold the infectivity of Chlamydia pneumoniae into L-929 cells, which suggests a possible IgG-mediated mechanism of entry and survival of the pathogen in fibroblast cells. [source] Fab crystallization and preliminary X-ray analysis of NC-1, an anti-HIV-1 antibody that recognizes the six-helix bundle core of gp41ACTA CRYSTALLOGRAPHICA SECTION F (ELECTRONIC), Issue 7 2010Lei Jin NC-1 is a murine monoclonal antibody that specifically recognizes the six-helix bundle core of the human immunodeficiency virus type 1 (HIV-1) gp41. As such, it is a useful tool for probing gp41 conformations in HIV-1 membrane fusion. To establish the structural basis underlying the NC-1 specificity, X-ray crystallography was employed to solve its three-dimensional structure. To accomplish this, hybridoma-produced NC-1 antibody was first purified and digested with papain. Its Fab fragment was then purified using size-exclusion chromatography following Fc depletion using a Protein A affinity column. Finally, crystallization of NC-1 Fab was performed by the hanging-drop vapour-diffusion method and the protein was crystallized at pH 8.0 using PEG 6000 as precipitant. The results showed that the NC-1 Fab crystals belonged to the trigonal space group P3221, with unit-cell parameters a = b = 118.7, c = 106.0,Å. There is one Fab molecule in the asymmetric unit, with 67.5% solvent content. An X-ray diffraction data set was collected at 3.2,Å resolution and a clear molecular-replacement solution was obtained for solution of the structure. [source] New approach in flow-cytometric determination of endotoxin during endotoxic shockBRITISH JOURNAL OF SURGERY (NOW INCLUDES EUROPEAN JOURNAL OF SURGERY), Issue 7 2000K.-H. Staubach Background Serum endotoxin was formerly measured with the non-specific Limulus lysate assay. The present approach was to quantitate the amount of endotoxin bound by peripheral mononuclear cells in order to develop a method for the diagnosis of early septic shock. Methods Using a murine monoclonal antibody (WN1-222/5), which binds highly specifically to lipopolysaccharide (LPS), a new method for measuring the amount of LPS bound to peripheral mononuclear cells was developed. Ten pigs were studied under sedation and peripheral mononuclear cells were taken every 4 h to determine the concentration of endotoxin by flow cytometry. The results are shown in the Table. Results Time after LPS infusion (h) 0 1 4 6 8 Marked cells (%) 32 61 75 72 85 The percentage of marked mononuclear cells increased during shock. Only in the last hours before death did the rate of increase decline. Conclusion Preliminary data on marked mononuclear cells showed that the amount of natural incorporated endotoxin, i.e. the quantity of bound endotoxin before infusion, was 32 per cent. © 2000 British Journal of Surgery Society Ltd [source] Functional Mimicry of an Anti-idiotypic Antibody to Nominal Antigen on Cellular ResponseCANCER SCIENCE, Issue 1 2002Jie Ma One concept for immune therapy of cancer involves induction of antigen mimic antibodies to trigger the immune system into a response against the tumor cells. Anti-idiotypic antibodies (Ab2) directed against the antigen-combining site of other antibodies (Ab1) may functionally and even structurally mimic antigen and induce anti-anti-idiotypic immune response. We report here the generation of murine monoclonal antibody (mAb) WJ02 (Ab2) raised against the murine monoclonal immunoglobulin MJ01 (Ab1), which defines ovarian cancer antigen CA125. In enzyme immunoassays the binding of Ab2 to the variable region of Ab1 could be inhibited by CA125. In addition, the mimicry of mAb WJ02 to CA125 on cellular immune response was detected by human peripheral blood cells. The T cells primed by mAb WJ02 or CA125 proliferated in the presence of CA125 or mAb WJ02, respectively. Furthermore, T cells specific to mAb WJ02 could lyse ovarian cancer cells OVCAR-3 that express CA125. Finally, we proved that a patient immunized with mAb MJ01 could induce T cells that recognize mAb WJ02. In summary, we conclude that mAb WJ02 mimics CA125 on cellular response and such functional mimicry is one of the most important criteria to select Ab2 for cancer therapy. [source] | ||||||||||