The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers
Antibodies to DNA (anti-DNA) are the serological hallmark of systemic lupus erythematosus (SLE) and can mediate disease pathogenesis by the formation of immune complexes. Since blocking immune complex formation can attenuate disease manifestations, the effects of nucleic acid binding polymers (NABPs...
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2012
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pubmed-33947502012-07-17 The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers Stearns, Nancy A. Lee, Jaewoo Leong, Kam W. Sullenger, Bruce A. Pisetsky, David S. Research Article Antibodies to DNA (anti-DNA) are the serological hallmark of systemic lupus erythematosus (SLE) and can mediate disease pathogenesis by the formation of immune complexes. Since blocking immune complex formation can attenuate disease manifestations, the effects of nucleic acid binding polymers (NABPs) on anti-DNA binding in vitro were investigated. The compounds tested included polyamidoamine dendrimer, 1,4-diaminobutane core, generation 3.0 (PAMAM-G3), hexadimethrine bromide, and a β-cylodextrin-containing polycation. As shown with plasma from patients with SLE, NABPs can inhibit anti-DNA antibody binding in ELISA assays. The inhibition was specific since the NABPs did not affect binding to tetanus toxoid or the Sm protein, another lupus autoantigen. Furthermore, the polymers could displace antibody from preformed complexes. Together, these results indicate that NABPs can inhibit the formation of immune complexes and may represent a new approach to treatment. Public Library of Science 2012-07-11 /pmc/articles/PMC3394750/ /pubmed/22808279 http://dx.doi.org/10.1371/journal.pone.0040862 Text en Stearns et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Stearns, Nancy A. Lee, Jaewoo Leong, Kam W. Sullenger, Bruce A. Pisetsky, David S. |
spellingShingle |
Stearns, Nancy A. Lee, Jaewoo Leong, Kam W. Sullenger, Bruce A. Pisetsky, David S. The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers |
author_facet |
Stearns, Nancy A. Lee, Jaewoo Leong, Kam W. Sullenger, Bruce A. Pisetsky, David S. |
author_sort |
Stearns, Nancy A. |
title |
The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers |
title_short |
The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers |
title_full |
The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers |
title_fullStr |
The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers |
title_full_unstemmed |
The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers |
title_sort |
inhibition of anti-dna binding to dna by nucleic acid binding polymers |
description |
Antibodies to DNA (anti-DNA) are the serological hallmark of systemic lupus erythematosus (SLE) and can mediate disease pathogenesis by the formation of immune complexes. Since blocking immune complex formation can attenuate disease manifestations, the effects of nucleic acid binding polymers (NABPs) on anti-DNA binding in vitro were investigated. The compounds tested included polyamidoamine dendrimer, 1,4-diaminobutane core, generation 3.0 (PAMAM-G3), hexadimethrine bromide, and a β-cylodextrin-containing polycation. As shown with plasma from patients with SLE, NABPs can inhibit anti-DNA antibody binding in ELISA assays. The inhibition was specific since the NABPs did not affect binding to tetanus toxoid or the Sm protein, another lupus autoantigen. Furthermore, the polymers could displace antibody from preformed complexes. Together, these results indicate that NABPs can inhibit the formation of immune complexes and may represent a new approach to treatment. |
publisher |
Public Library of Science |
publishDate |
2012 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394750/ |
_version_ |
1611542474917937152 |