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Complement Inhibitors in Clinical Trials for Glomerular Diseases
Defective complement action is a cause of several human glomerular diseases including atypical hemolytic uremic syndrome (aHUS), anti-neutrophil cytoplasmic antibody mediated vasculitis (ANCA), C3 glomerulopathy, IgA nephropathy, immune complex membranoproliferative glomerulonephritis, ischemic repe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776600/ https://www.ncbi.nlm.nih.gov/pubmed/31611870 http://dx.doi.org/10.3389/fimmu.2019.02166 |
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author | Zipfel, Peter F. Wiech, Thorsten Rudnick, Ramona Afonso, Sara Person, Fermin Skerka, Christine |
author_facet | Zipfel, Peter F. Wiech, Thorsten Rudnick, Ramona Afonso, Sara Person, Fermin Skerka, Christine |
author_sort | Zipfel, Peter F. |
collection | PubMed |
description | Defective complement action is a cause of several human glomerular diseases including atypical hemolytic uremic syndrome (aHUS), anti-neutrophil cytoplasmic antibody mediated vasculitis (ANCA), C3 glomerulopathy, IgA nephropathy, immune complex membranoproliferative glomerulonephritis, ischemic reperfusion injury, lupus nephritis, membranous nephropathy, and chronic transplant mediated glomerulopathy. Here we summarize ongoing clinical trials of complement inhibitors in nine glomerular diseases and show which inhibitors are used in trials for these renal disorders (http://clinicaltrials.gov). |
format | Online Article Text |
id | pubmed-6776600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67766002019-10-14 Complement Inhibitors in Clinical Trials for Glomerular Diseases Zipfel, Peter F. Wiech, Thorsten Rudnick, Ramona Afonso, Sara Person, Fermin Skerka, Christine Front Immunol Immunology Defective complement action is a cause of several human glomerular diseases including atypical hemolytic uremic syndrome (aHUS), anti-neutrophil cytoplasmic antibody mediated vasculitis (ANCA), C3 glomerulopathy, IgA nephropathy, immune complex membranoproliferative glomerulonephritis, ischemic reperfusion injury, lupus nephritis, membranous nephropathy, and chronic transplant mediated glomerulopathy. Here we summarize ongoing clinical trials of complement inhibitors in nine glomerular diseases and show which inhibitors are used in trials for these renal disorders (http://clinicaltrials.gov). Frontiers Media S.A. 2019-09-27 /pmc/articles/PMC6776600/ /pubmed/31611870 http://dx.doi.org/10.3389/fimmu.2019.02166 Text en Copyright © 2019 Zipfel, Wiech, Rudnick, Afonso, Person and Skerka. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Zipfel, Peter F. Wiech, Thorsten Rudnick, Ramona Afonso, Sara Person, Fermin Skerka, Christine Complement Inhibitors in Clinical Trials for Glomerular Diseases |
title | Complement Inhibitors in Clinical Trials for Glomerular Diseases |
title_full | Complement Inhibitors in Clinical Trials for Glomerular Diseases |
title_fullStr | Complement Inhibitors in Clinical Trials for Glomerular Diseases |
title_full_unstemmed | Complement Inhibitors in Clinical Trials for Glomerular Diseases |
title_short | Complement Inhibitors in Clinical Trials for Glomerular Diseases |
title_sort | complement inhibitors in clinical trials for glomerular diseases |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776600/ https://www.ncbi.nlm.nih.gov/pubmed/31611870 http://dx.doi.org/10.3389/fimmu.2019.02166 |
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