The sera from three C8 alpha-gamma deficient patients previously reported to have a selective C8 alpha-gamma defect were analyzed by SDS-PAGE and Western blot using two polyclonal antisera to C8 alpha-gamma and a monoclonal antibody to C8 alpha. All three sera exhibited C8 alpha-gamma bands that dissociated into alpha and gamma chains under reducing conditions. Quantitation of the alpha-gamma subunit in these sera by a sensitive ELISA revealed an amount approximately 1% of that found in normal human serum. A similar assay performed with a specific antiserum to C8 beta showed unexpectedly low levels of C8 beta in these sera, which were confirmed by hemolytic titration of C8 beta. The remarkable differences between C8 alpha-gamma and C8 beta in the C8 alpha-gamma deficient sera was that in spite of their comparable immunochemical levels, C8 beta still exhibited functional activity whereas C8 alpha-gamma was totally inactive. That the residual C8 alpha-gamma was inactive was also proved by its inability to show lytic bands in an overlay system after SDS-PAGE and subsequent removal of SDS. The implications of these findings for a novel concept of C8 deficiency are discussed.
F Tedesco, L Roncelli, B H Petersen, V Agnello, J M Sodetz
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Complement in human diseases: Lessons from complement deficiencies
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Molecular Immunology | 2009 |
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JCR: Journal of Clinical Rheumatology | 2006 |
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Mannose binding lectin and C3 act as recognition molecules for infectious agents in the vagina
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Journal of immunology (Baltimore, Md. : 1950) | 2003 |
Hepatocyte Nuclear Factor 1α Controls the Expression of Terminal Complement Genes
M Pontoglio, M Pausa, A Doyen, B Viollet, M Yaniv, F Tedesco |
Journal of Experimental Medicine | 2001 |
The endothelium is an extrahepatic site of synthesis of the seventh component of the complement system
H Langeggen, M Pausa, E Johnson, C Casarsa, F Tedesco |
Clinical & Experimental Immunology | 2000 |
The Complement FactsBook
LB Klickstein, JM Moulds |
The Complement FactsBook | 2000 |
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The cytolytically inactive terminal complement complex activates endothelial cells to express adhesion molecules and tissue factor procoagulant activity
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In vitro expression of the beta subunit of human complement component C8
CS Letson, KM Kaufman, JM Sodetz |
Molecular Immunology | 1996 |
Biosynthesis of C3 by human mesangial cells. Modulation by proinflammatory cytokines
V Montinaro, L Serra, S Perissutti, E Ranieri, F Tedesco, FP Schena |
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Genomic organization of human complement protein C8? and further examination of its linkage to C8?
GA Michelotti, JV Snider, JM Sodetz |
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Effect of cytokines on the secretion of the fifth and eighth complement components by HepG2 cells
S Perissutti, F Tedesco |
International Journal of Clinical & Laboratory Research | 1994 |
Inherited Deficiencies of the Terminal Complement Components
F Tedesco, W Nürnberger, S Perissutti |
International Reviews of Immunology | 1993 |
Antibody Response to Meningococcal Polysaccharides A and C in Patients with Complement Defects
R Biselli, I Casapollo, R D'amelio, S Salvato, PM Matricardi, M Brai |
Scandinavian Journal of Immunology | 1993 |
The Complement System
A Agostoni, M Cicardi, M Gardinali, L Bergamaschini |
International journal of immunopathology and pharmacology | 1992 |
Infectious diseases associated with complement deficiencies
JE Figueroa, P Densen |
Clinical microbiology reviews | 1991 |
Genetic deficiency of complement component C8 in the rabbit: Evidence of a translational defect in expression of the ?-? subunit
M Komatsu, KI Yamamoto, H Mikami, JM Sodetz |
Biochemical Genetics | 1991 |