Abstract

Complement alternative pathway dysregulation seems to be the pathophysiological basis of Dense Deposit Disease (DDD). Here, we describe a monoclonal anti-factor H (FH) autoantibody in a woman diagnosed with DDD with a monoclonal gammapathy. Enzyme-linked immunosorbent assays evidenced the presence of anti-FH antibodies in the patient's serum and showed that they were associated with the monoclonal IgG-λ fraction. These autoantibodies recognize the N-terminal region of FH and interfere with its regulatory function. In summary, in the DDD patient described here, the activation of complement alternative pathway was favoured by the presence of anti-FH autoantibodies that recognize the regulatory region of this protein and impede its function and which could ultimately cause the glomerulopathy.

Details

Title
Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease
Author
Nozal, Pilar 1 ; Strobel, Stefanie 2 ; Ibernon, Meritxell 3 ; López, Dolores 4 ; Sánchez-Corral, Pilar 5 ; Rodríguez de Córdoba, Santiago 6 ; Józsi, Mihály 2 ; López-Trascasa, Margarita 7 

 Unidad de Inmunología, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain 
 Leibniz Institute for Natural Product Research and Infection Biology—Hans Knöll Institute, Jena, Germany 
 Nephrology Department, Hospital Germans Trias i Pujol, Badalona, Spain 
 Pathology Department, Hospital Germans Trias i Pujol, Barcelona, Spain 
 Unidad de Investigación, Hospital Universitario La Paz, IdiPAZ, CIBERER U754, Madrid, Spain 
 Centro de Investigaciones Biológicas, CSIC, CIBERER U 738, Madrid, Spain 
 Unidad de Inmunología, Hospital Universitario La Paz, IdiPAZ, CIBERER U 754, Madrid, Spain 
Pages
133-136
Publication year
2012
Publication date
Apr 2012
Publisher
Oxford University Press
ISSN
20488505
e-ISSN
20488513
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3170125194
Copyright
© The Author 2012. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For permissions, please e-mail: [email protected]. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.