Go to JCI Insight
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact
  • Clinical Research and Public Health
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Gastroenterology
    • Immunology
    • Metabolism
    • Nephrology
    • Neuroscience
    • Oncology
    • Pulmonology
    • Vascular biology
    • All ...
  • Videos
    • Conversations with Giants in Medicine
    • Video Abstracts
  • Reviews
    • View all reviews ...
    • Complement Biology and Therapeutics (May 2025)
    • Evolving insights into MASLD and MASH pathogenesis and treatment (Apr 2025)
    • Microbiome in Health and Disease (Feb 2025)
    • Substance Use Disorders (Oct 2024)
    • Clonal Hematopoiesis (Oct 2024)
    • Sex Differences in Medicine (Sep 2024)
    • Vascular Malformations (Apr 2024)
    • View all review series ...
  • Viewpoint
  • Collections
    • In-Press Preview
    • Clinical Research and Public Health
    • Research Letters
    • Letters to the Editor
    • Editorials
    • Commentaries
    • Editor's notes
    • Reviews
    • Viewpoints
    • 100th anniversary
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • Reviews
  • Review series
  • Conversations with Giants in Medicine
  • Video Abstracts
  • In-Press Preview
  • Clinical Research and Public Health
  • Research Letters
  • Letters to the Editor
  • Editorials
  • Commentaries
  • Editor's notes
  • Reviews
  • Viewpoints
  • 100th anniversary
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact

Citations to this article

Two distinct abnormalities in patients with C8 alpha-gamma deficiency. Low level of C8 beta chain and presence of dysfunctional C8 alpha-gamma subunit.
F Tedesco, … , V Agnello, J M Sodetz
F Tedesco, … , V Agnello, J M Sodetz
Published September 1, 1990
Citation Information: J Clin Invest. 1990;86(3):884-888. https://doi.org/10.1172/JCI114789.
View: Text | PDF
Research Article

Two distinct abnormalities in patients with C8 alpha-gamma deficiency. Low level of C8 beta chain and presence of dysfunctional C8 alpha-gamma subunit.

  • Text
  • PDF
Abstract

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.

Authors

F Tedesco, L Roncelli, B H Petersen, V Agnello, J M Sodetz

×

Total citations by year

Year: 2020 2016 2010 2009 2006 2005 2003 2001 2000 1998 1997 1996 1995 1994 1993 1992 1991 Total
Citations: 2 2 1 1 1 2 1 1 2 1 1 1 2 1 2 1 2 24
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article (24)

Title and authors Publication Year
A Point Mutation Creating a 3′ Splice Site in C8A Is a Predominant Cause of C8α-γ Deficiency in African Americans
P Densen, L Ackermann, L Saucedo, JE Figueroa, Z Si, CM Stoltzfus
Journal of immunology (Baltimore, Md. : 1950) 2020
A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report
M Jiang, S Wang, F Li, J Geng, Y Ji, K Li, X Jiang
Medicine 2020
Textbook of Pediatric Rheumatology
E Silverman, J Buyon, E Jaeggi
Textbook of Pediatric Rheumatology 2016
Pediatric Allergy: Principles and Practice
J Wang, HA Sampson
Pediatric Allergy: Principles and Practice 2016
Infections of People with Complement Deficiencies and Patients Who Have Undergone Splenectomy
S Ram, LA Lewis, PA Rice
Clinical microbiology reviews 2010
Complement in human diseases: Lessons from complement deficiencies
M Botto, M Kirschfink, P Macor, MC Pickering, R Würzner, F Tedesco
Molecular Immunology 2009
Systemic Lupus Erythematosus
M Petri
JCR: Journal of Clinical Rheumatology 2006
Thrombus formation induced by antibodies to beta2-glycoprotein I is complement dependent and requires a priming factor
F Fischetti, P Durigutto, V Pellis, A Debeus, P Macor, R Bulla, F Bossi, F Ziller, D Sblattero, P Meroni, F Tedesco
Blood 2005
Mannose binding lectin and C3 act as recognition molecules for infectious agents in the vagina
V Pellis, FD Seta, S Crovella, F Bossi, R Bulla, S Guaschino, O Radillo, P Garred, F Tedesco
Clinical & Experimental Immunology 2005
Serum-Resistant Strains of Borrelia burgdorferi Evade Complement-Mediated Killing by Expressing a CD59-Like Complement Inhibitory Molecule
M Pausa, V Pellis, M Cinco, PG Giulianini, G Presani, S Perticarari, R Murgia, F Tedesco
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
Characterization of Soluble Terminal Complement Complex Assembled in C8beta-Deficient Plasma and Serum
Hogasen, Mollnes, Nurnberger, Pausa, Fukumori, Tedesco
Scandinavian Journal of Immunology 1998
The cytolytically inactive terminal complement complex activates endothelial cells to express adhesion molecules and tissue factor procoagulant activity
F Tedesco, M Pausa, E Nardon, M Introna, A Mantovani, A Dobrina
Journal of Experimental Medicine 1997
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
Kidney International 1995
Genomic organization of human complement protein C8? and further examination of its linkage to C8?
GA Michelotti, JV Snider, JM Sodetz
Human Genetics 1995
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

Advertisement

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

Sign up for email alerts