Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.

Systemic lupus erythematosus is characterized by dysfunctional clearance of apoptotic debris and the development of pathogenic autoantibodies. While the complement system is also involved in the disease no attempt has been made to generate a comprehensive view of immune complex formation from variou...

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Main Authors: Krisztián Papp, Péter Végh, Renáta Hóbor, Zoltán Szittner, Zoltán Vokó, János Podani, László Czirják, József Prechl
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3439431?pdf=render
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author Krisztián Papp
Péter Végh
Renáta Hóbor
Zoltán Szittner
Zoltán Vokó
János Podani
László Czirják
József Prechl
author_facet Krisztián Papp
Péter Végh
Renáta Hóbor
Zoltán Szittner
Zoltán Vokó
János Podani
László Czirják
József Prechl
author_sort Krisztián Papp
collection DOAJ
description Systemic lupus erythematosus is characterized by dysfunctional clearance of apoptotic debris and the development of pathogenic autoantibodies. While the complement system is also involved in the disease no attempt has been made to generate a comprehensive view of immune complex formation from various autoantigens. We increased the complexity of autoantibody profiles by measuring the binding of two complement proteins, C3 and C4, in addition to two antibody classes, IgG and IgM, to a collection of autoantigens. These complement components covalently bind to those microarray features where antibodies and other serum components induce complement activation. Using this technology, we compared functional serum antibody profiles of control subjects (n = 31) and patients with lupus erythematosus (n = 61) in the active (n = 22) and inactive (n = 39) phase of the disease. Multivariate analysis was applied to identify contributions of binding data on 25 antigens to the discrimination of the study groups. Receiver operating characteristic analysis was used to portray the discriminative property of each measured parameter for each antigen in pairwise group comparisons. Complement C3 and C4 deposition increased on autoantibody targets in spite of the decreased serum complement concentrations, and decreased on other autoantigens, demonstrating the imbalance of complement function in patients with lupus erythematosus. Our observations confirmed previously known markers of disease and showed that C3 and C4 deposition data were at least as powerful as Ig binding data in separating the study groups.
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spelling doaj.art-8f31296bd34c451a811ff3e8492eb35a2022-12-22T03:35:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4482410.1371/journal.pone.0044824Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.Krisztián PappPéter VéghRenáta HóborZoltán SzittnerZoltán VokóJános PodaniLászló CzirjákJózsef PrechlSystemic lupus erythematosus is characterized by dysfunctional clearance of apoptotic debris and the development of pathogenic autoantibodies. While the complement system is also involved in the disease no attempt has been made to generate a comprehensive view of immune complex formation from various autoantigens. We increased the complexity of autoantibody profiles by measuring the binding of two complement proteins, C3 and C4, in addition to two antibody classes, IgG and IgM, to a collection of autoantigens. These complement components covalently bind to those microarray features where antibodies and other serum components induce complement activation. Using this technology, we compared functional serum antibody profiles of control subjects (n = 31) and patients with lupus erythematosus (n = 61) in the active (n = 22) and inactive (n = 39) phase of the disease. Multivariate analysis was applied to identify contributions of binding data on 25 antigens to the discrimination of the study groups. Receiver operating characteristic analysis was used to portray the discriminative property of each measured parameter for each antigen in pairwise group comparisons. Complement C3 and C4 deposition increased on autoantibody targets in spite of the decreased serum complement concentrations, and decreased on other autoantigens, demonstrating the imbalance of complement function in patients with lupus erythematosus. Our observations confirmed previously known markers of disease and showed that C3 and C4 deposition data were at least as powerful as Ig binding data in separating the study groups.http://europepmc.org/articles/PMC3439431?pdf=render
spellingShingle Krisztián Papp
Péter Végh
Renáta Hóbor
Zoltán Szittner
Zoltán Vokó
János Podani
László Czirják
József Prechl
Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.
PLoS ONE
title Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.
title_full Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.
title_fullStr Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.
title_full_unstemmed Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.
title_short Immune complex signatures of patients with active and inactive SLE revealed by multiplex protein binding analysis on antigen microarrays.
title_sort immune complex signatures of patients with active and inactive sle revealed by multiplex protein binding analysis on antigen microarrays
url http://europepmc.org/articles/PMC3439431?pdf=render
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