Erythrocytes of patients with paroxysmal nocturnal haemoglobinuria acquire resistance to complement attack by purified 20-kD homologous restriction factor
N. OKADA
Department of Microbiology, Fukuoka University School of Medicine, Nanakuma, Fukuoka
Search for more papers by this authorR. HARADA
Department of Microbiology, Fukuoka University School of Medicine, Nanakuma, Fukuoka
Search for more papers by this authorCorresponding Author
H. OKADA
Department of Molecular Biology, Nagoya City University School of Medicine, Nagoya, Japan
Dr Noriko Okada, Department of Microbiology, Fukuoka University School of Medicine, Nanakuma 7-45-1, Fukuoka 814-01, Japan.Search for more papers by this authorN. OKADA
Department of Microbiology, Fukuoka University School of Medicine, Nanakuma, Fukuoka
Search for more papers by this authorR. HARADA
Department of Microbiology, Fukuoka University School of Medicine, Nanakuma, Fukuoka
Search for more papers by this authorCorresponding Author
H. OKADA
Department of Molecular Biology, Nagoya City University School of Medicine, Nagoya, Japan
Dr Noriko Okada, Department of Microbiology, Fukuoka University School of Medicine, Nanakuma 7-45-1, Fukuoka 814-01, Japan.Search for more papers by this authorSUMMARY
A 20-kD homologous restriction factor (HRF20) which is a membrane inhibitor of the terminal stage of human complement action can be detected by the monoclonal antibody IF5, and is deficient on abnormal erythrocytes as well as leucocytes from patients with paroxysmal nocturnal haemoglobinuria (PNH). The erythrocytes of PNH patients significantly improved their resistance to homologous complement after adsorption of purified HRF20.
REFERENCES
- Dacie, J.V. & Richardson, N. (1943) The influence of pH on in vitro haemolysis in nocturnal haemoglobinuria. J. pathol. Bacterial. 55, 375.
- Ey, P.L., Prowse, S.J. & Jenkin, C.R. 1978) Isolation of pure IgGl, IgG2a and IgG2b immunoglobulins from mouse serum using protein A Sepharose, Immunochemistry. 15, 429.
- Fujita, T., Inoue, T., Ogawa, K., Iida, K., Iida, K, & Tamura, N. (1987) The mechanism of action of decay-accelerating factor (DAF). DAF inhibits the assembly of C3 convertase by dissociating C2a and Bb, J. exp. Med. 166, 1221.
- Hartmann, R.C. & Jenkins, D.E. Jr (1966) The sugar-water test for paroxysmal nocturnal hemoglobinuria. N. Engl. J. Med. 275, 155.
- Hoffmann, E.M. (1969) Inhibition of complement by a substance isolated from human erythrocytes. I, Extraction from human erythrocytes stroma. Immunuochemistry. 6, 391.
- Holguin, M.H., Fredrick, L.R., Bernshaw, N.J., Welcox, L.A. & Parker, C.J. (1989) Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes of paroxysmal nocturnal hemoglobinuria. J. clin. Invest. 84, 7.
- Laemmli, U.K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 227, 680.
- Logue, G.L., Rosse, W.F. & Adams, J.P. (1973) Mechanism of immune lysis of red blood cells in vitro. 1. PNH cells. J. clin. Invest. 52, 1129.
- Medof, E., Kinoshita, T. & Nussenzweig, V. (1984) Inhibition of complement activation on the surface of cells after incorporation of decay accelerating factor (DAF) into their membranes. J. exp. Med. 160, 1558.
- Nicholson-Weller, A., Burge, J., Fearon, D.T., Weller, P.F. & Austen, K.F. (1982) Isolation of a human erythrocytes membrane glycoprotein with decay-accelerating activity for C3 convertases of the complement system. J. Immunol. 29, 184.
- Nicholson-Weller, A., March, J.P., Rosenfeld, S.I. & Austen, K.F. (1983) Affected erythrocytes of patients with paroxysmal hemoglobinuria and deficient in the complement regulatory protein, decay accelerating factor. Proc. natl Acad. Sci. USA. 80, 5066.
- Okada, H., Tanaka, H. & Okada, N. (1983) Prevention of complement activation on the homologous cell membrane of nucleated cells as well as erythrocytes. Eur. J. Immunol. 13, 340.
- Okada, N., Harada, R., Fujita, T. & Okada, H. (1989a) A novel membrane glycoprotein capable of inhibiting membrane attack by homologous complement. J. Immunol. 1, 205.
- Okada, N., Harada, R., Fujita, T. & Okada, H. (1989b) Monoclonal antibodies capable of causing hemolysis of neuraminidase-treated human erythrocytes by homologous complement. J. Immunol. 143, 2262.
- Okada, H., Nagami, Y., Takahashi, K., Okada, N., Hideshima, T., Takizawa, H. & Kondo, J. (1989c) 20KDa homologous restriction factor of complement resembles T cell activating protein Biochim. Biophys. Res. Commun. 165, 165, 1553.
- Okada, N., Harada, R., Hideshima, T., Kameyoshi, Y. & Okada, H.(1987) Anti-human erythrocyte monoclonal antibody which causes hemolysis of human erythrocytes mediated by the alternative pathway of human complment. Proc. Jap. Soc. Immunol. 17, 498 (Abstract).
- Pangburn, M.K., Schreiber, R.D. & Müller-Eberhard, H.J. (1981) Formation of the initial C3 convertase of the alternative complement pathway. Acquisition of C3b-like activities by spontaneous hydrolysis of the putative thioester in native C3. J. exp. Med. 154, 856.
- Pangburn, M.K., Schreiber, R.P. & Müuller-Eberhard, H.J. (1983a)Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria. Proc. natl Acad. Sci. USA, 80, 5430.
- Pangburn, M.K., Schreiber, R.D., Trombold, J.S. & Müuller-Eberhard, H.J. (1983b) Paroxysmal nocturnal hemoglobinuria; deficiency in factor H like functions of the abnormal erythrocytes. J. exp. Med. 157, 1971.
- Schonermark, S., Rauterberg, E.W. Shin, M.L., Loke, S., Roelcke, D. & Hänsh, G.M. (1986) Homologous species restriction in lysis of human erythrocytes: a membrane-derived protein with C8-binding capacity functions as an inhibitor. J. Immunol. 136, 1772.
- Schreiber, R.D., Morrison, D. C., Podack, E.R. & Müller-Eberhard, H.J. (1979) Bactericidal activity of the alternative complement pathway generated from 11 isolated plasma proteins. J. exp. Med. 149, 870.
- Sugita, Y., Nakano, Y. & Tomita, M. (1988) Isolation from human erythrocytes of a new membrane protein which inhibits the formation of complement transmembrane channels. J. Biochem. 104, 633.
- Zalman, L.S., Wood, L.M. & Müller-Eberhard, H.J. (1986) Isolation of a human erythrocyte membrane protein capable of Inhibiting expression of homologous complement transmembrane channels. Proc. natl Acad. Sci. USA, 83, 6975.
- Zalman, L.S., Wood, L.M., Frank, M.M. & Müller-Eberhard, H.J.(1987) Deficiency of the homologous restriction factor in paroxysmal nocturnal hemoglobinuria. J. exp. Med, 165, 572.