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Inhibitory short synthetic oligodeoxynucleotides and lupus
B cells and antigen-presenting cells express a group of intracellular Toll-like receptors (TLRs) that recognize nucleic acids and can be accessed only when apoptotic debris or immune complexes are internalized by B-cell receptors or Fc receptors. This results in rapid cell activation and release of...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714142/ https://www.ncbi.nlm.nih.gov/pubmed/19591639 http://dx.doi.org/10.1186/ar2726 |
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author | Liu, Zheng Davidson, Anne |
author_facet | Liu, Zheng Davidson, Anne |
author_sort | Liu, Zheng |
collection | PubMed |
description | B cells and antigen-presenting cells express a group of intracellular Toll-like receptors (TLRs) that recognize nucleic acids and can be accessed only when apoptotic debris or immune complexes are internalized by B-cell receptors or Fc receptors. This results in rapid cell activation and release of inflammatory mediators that perpetuate the autoantibody response. TLR-7 and TLR-9 are required to generate autoantibodies to RNA and DNA, respectively. Synthetic oligodeoxynucleotides that inhibit the activity of these intracellular TLRs attenuate systemic lupus erythematosus in mouse models and may be of therapeutic benefit in human systemic lupus erythematosus. |
format | Text |
id | pubmed-2714142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27141422009-07-22 Inhibitory short synthetic oligodeoxynucleotides and lupus Liu, Zheng Davidson, Anne Arthritis Res Ther Editorial B cells and antigen-presenting cells express a group of intracellular Toll-like receptors (TLRs) that recognize nucleic acids and can be accessed only when apoptotic debris or immune complexes are internalized by B-cell receptors or Fc receptors. This results in rapid cell activation and release of inflammatory mediators that perpetuate the autoantibody response. TLR-7 and TLR-9 are required to generate autoantibodies to RNA and DNA, respectively. Synthetic oligodeoxynucleotides that inhibit the activity of these intracellular TLRs attenuate systemic lupus erythematosus in mouse models and may be of therapeutic benefit in human systemic lupus erythematosus. BioMed Central 2009 2009-06-26 /pmc/articles/PMC2714142/ /pubmed/19591639 http://dx.doi.org/10.1186/ar2726 Text en Copyright © 2009 BioMed Central Ltd |
spellingShingle | Editorial Liu, Zheng Davidson, Anne Inhibitory short synthetic oligodeoxynucleotides and lupus |
title | Inhibitory short synthetic oligodeoxynucleotides and lupus |
title_full | Inhibitory short synthetic oligodeoxynucleotides and lupus |
title_fullStr | Inhibitory short synthetic oligodeoxynucleotides and lupus |
title_full_unstemmed | Inhibitory short synthetic oligodeoxynucleotides and lupus |
title_short | Inhibitory short synthetic oligodeoxynucleotides and lupus |
title_sort | inhibitory short synthetic oligodeoxynucleotides and lupus |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714142/ https://www.ncbi.nlm.nih.gov/pubmed/19591639 http://dx.doi.org/10.1186/ar2726 |
work_keys_str_mv | AT liuzheng inhibitoryshortsyntheticoligodeoxynucleotidesandlupus AT davidsonanne inhibitoryshortsyntheticoligodeoxynucleotidesandlupus |