[en] The haem enzyme myeloperoxidase (MPO) (EC 1.11.1.7) with a spectral A430/A280 ratio greater than 0.7 and a specific activity of 125 U/mg was purified from isolated human neutrophils. To obtain a radioimmunoassay (RIA) for this enzyme, a specific antiserum against human neutrophil MPO was raised in rabbits and used at an initial dilution of 1/10,000. MPO labelled with 125iodine by a technique of self-labelling in the presence of H2O2, had a specific activity of 24 mCi/mg. After incubation at room temperature (2 h) and separation by double antibody precipitation in the presence of polyethylene glycol, the sensitivity of the RIA was 21 ng/ml. The RIA showed good precision and accuracy with intra- and interassay coefficients of variation of less than 7% for MPO concentrations ranging from 100 to 800 ng/ml, and satisfactory recoveries of known amounts of exogenous MPO in plasma. For the measurement of MPO in blood, the best sampling technique was to collect blood into EDTA. Rapid centrifugation (within 20 min) was necessary for blood collected into heparin. Mean MPO values in normal individuals were 340 +/- 98 ng/ml in EDTA plasma (n = 152) and 332 +/- 82 ng/ml in heparinized plasma (n = 34). When MPO was measured 12-6 h after injury in critically ill patients high values (above 1000 ng/ml) were found in 6/15 patients with multiple injuries. In patients with sepsis (n = 22), MPO values were always above 1000 ng/ml.
Disciplines :
Anesthesia & intensive care
Author, co-author :
Pincemail, Joël ; Centre Hospitalier Universitaire de Liège - CHU > Chirurgie cardio-vasculaire
Deby-Dupont, G.
Deby, Christiane ; Centre Hospitalier Universitaire de Liège - CHU > Service administration des patients
Thirion, Anne-Marie ; Université de Liège - ULiège > Services généraux (Fac. de psycho. et des sc. de l'éducat.) > Relations académiques et scientifiques (Psycho et sc.éduc.)
Andrews, Krinsky (1981) The reductive cleavage of myeloperoxidase in half, producing enzymatically active hemi-myeloperoxidase. J. Biol. Chem. 256:4211.
Badwey, Karnovsky (1980) Active oxygen species and the function of phagocytic leukocytes. Ann. Rev. Biochem. 49:695.
Baker, O'Neil (1976) The injury severity score: an update. J. Trauma 16:882.
Bakkenist, Wever, Vulsma, Plat, Van Gelder (1978) Isolation procedure and some properties of myeloperoxidase from human leukocytes. Biochim. Biophys. Acta 524:45.
Bentwood, Henson (1980) The sequential release of granule constituents from human neutrophils. J. Immunol. 124:855.
Borgeat, Samuelsson (1979) Arachidonic acid metabolism in polymorphonuclear leukocytes: Effects of ionophore A23187. Proc. Natl. Acad. Sci. U.S.A. 76:2148.
Deby-Dupont, Pincemail, Thirion, Deby (1987) A radioimmunoassay for polymorphonuclear leukocytes myeloperoxidase: preliminary results. Arch. Int. Physiol. Biochem. 95:S9.
Deby-Dupont, Pincemal, Reuter (1988) Iodination of polymorphonuclear leucocytes myeloperoxydase. Archives Of Physiology And Biochemistry 96:B25.
Dittmer, Jochum, Schmidt-Neuerburg (1985) Der PMN-Elastase-Plasmaspiegel, ein biochemischer Parameter der Traumaschwere. Chirurgia 56:723.
Ekins (1969) Problems of sensitivity with special reference to optimal conditions. Protein and Polypeptides hormones , M. Margoulis, Excerpta Medica Foundation ICS 161, Amsterdam; 672.
Hansen, Malmquist, Thorell (1975) Plasma myeloperoxidase and lactoferrin measured by radioimmunoassay: relations to neutrophils kinetics. Acta Med. Scand. 198:437.
Jochum, Witte, Duswald, Inthorn, Welter, Fritz (1986) Pathobiochemistry of sepsis role of proteinases proteinase inhibitors and oxidizing agents. Behring Inst Mitt 79:121.
Klebanoff (1968) Myeloperoxidase-halide-hydrogen peroxide anti-bacterial system. J. Bacteriol. 95:2131.
Klebanoff (1988) Phagocytic cells: products of oxygen metabolism. Inflammation: Basic Principles and Clinical Correlates , J.I. Gallin, I.M. Golstein, R. Snyderman, Raven Press, New-York; 391.
Neumann, Gunzer, Lang, Jochum, Fritz (1986) Quantitation of myeloperoxidase from human granulocytes as an inflammation marker by enzyme-linked immunosorbent assay. Fresenius Z. Anal. Chem. 324:365.
Öberg, Dahl, Ellegaard, Sundström, Vaeth, Venge (1987) Diagnostic and prognostic significance of serum measurements of lactoferrin, lysozyme and myeloperoxidase in acute myeloid leukemia (AML): recognition of a new variant, high-lactoferrin AML. J. Haematol. 38:148.
Olofsson, Olsson, Venge, Elgefors (1977) Serum myeloperoxidase and lactoferrin in neutropenia. Scand. J. Haematol. 18:73.
Olofsson, Olsson, Venge (1977) Myeloperoxidase and lactoferrin of blood neutrophils and plasma in chronic granulocytic leukemia. Scand. J. Haematol. 18:113.
Olsen, Steigen, Holm, Little (1986) Molecular forms of myeloperoxidase in human plasma. Biochem. J. 237:559.
Olsson (1987) Regulation of myelopoiesis and maturation of phagocyte functions. Eur. J. Clin. Invest. 17:A57.
Olsson, Olofsson, Ohlsson, Gustavsson (1979) Serum and plasma myeloperoxidase, elastase and lactoferrin content in acute myeloid leukaemia. Scand. J. Haematol. 22:397.
Roth, Bendayan, Carlemalm, Villinger, Garavito (1981) Enhancement of structural preservation and immunocyto-chemical staining in low temperature embedded pancreatic tissues. J. Histochem. Cytochem. 29:663.
Simon, Ward (1988) Adult Respiratory Distress Syndrome. Inflammation: Basic Principles and Clinical Correlates , J.I. Gallin, I.M. Goldstein, R. Snyderman, Raven Press, New York; 815.
Svensson, Domeij, Lindvall, Rydell (1987) Peroxidase and peroxidase-oxidase activities of isolated human myeloperoxidase. Biochem. J. 242:673.
Thorell, Larsson (1974) Lactoperoxidase coupled to polyacrylamide for radioiodination of proteins to high specific activity. Immunochemistry 11:203.
Vaitukaitis, Robbins, Nieschlag, Ross (1971) A method for producing specific antisera with small doses of immunogen. J. Clin. Endocrinol. 33:988.
Venge, Hällgren, Stalenheim, Olsson (1979) Effects of serum and cations on the selective release of granular proteins from human neutrophils during phagocytosis. Scand. J. Haematol. 22:317.
Wood, Stella, Muller, Scriba (1979) A rapid and specific method for separation of bound and free antigen in radioimmunoassay systems. J. Clin. Chem. Clin. Biochem. 17:111.
Zgliczynski, Stelmaseynska, Domanski, Ostrowski (1971) Chloramines as indermediates of oxidation reaction of amino acids by myeloperoxidase. Biochimica et Biophysica Acta (BBA) - Enzymology 235:419.