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BAFF and APRIL expression as an autoimmune signature of membranous nephropathy
BACKGROUND: Based on the fact that B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) have a regulatory role in B cell biology, excessive levels of these cytokines can promote autoimmune pathogenesis. However, the expression and implication remain unresolved in cases of memb...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790464/ https://www.ncbi.nlm.nih.gov/pubmed/29423047 http://dx.doi.org/10.18632/oncotarget.23232 |
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author | Han, Seung Seok Yang, Seung Hee Jo, Hyung Ah Oh, Yun Jung Park, Minkyoung Kim, Joo Young Lee, Hajeong Lee, Jung Pyo Lee, Sang-Ho Joo, Kwon Wook Lim, Chun Soo Kim, Yon Su Kim, Dong Ki |
author_facet | Han, Seung Seok Yang, Seung Hee Jo, Hyung Ah Oh, Yun Jung Park, Minkyoung Kim, Joo Young Lee, Hajeong Lee, Jung Pyo Lee, Sang-Ho Joo, Kwon Wook Lim, Chun Soo Kim, Yon Su Kim, Dong Ki |
author_sort | Han, Seung Seok |
collection | PubMed |
description | BACKGROUND: Based on the fact that B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) have a regulatory role in B cell biology, excessive levels of these cytokines can promote autoimmune pathogenesis. However, the expression and implication remain unresolved in cases of membranous nephropathy (MN). RESULTS: The plasma BAFF levels of the primary MN patients were higher than those of healthy controls but lower than those of secondary MN patients, whereas the APRIL levels were similar between the MN patients and healthy controls. The BAFF levels were higher in relapse cases, whereas the APRIL levels were higher in the patients who did not experience remission compared with the counterpart patients. The ectopic expression of BAFF and APRIL was observed in the glomeruli or circulating B cells of MN patients, and this high expression trend was similar to that of lupus patients. CONCLUSIONS: Expression profile of BAFF and APRIL in MN is similar to that of other autoimmune disease, which affects the kidney outcomes. METHODS: Plasma BAFF and APRIL levels were measured upon kidney biopsy in patients with primary (n = 89) and secondary MN (n = 13), and the results were compared with the levels in healthy controls (n = 111). The kidney outcomes (e.g., remission and relapse) were traced for the median of 3 years. Aberrant expression of the cytokines was evaluated in the kidney and circulating B cells using immunohistochemistry and flow cytometry analyses, respectively. |
format | Online Article Text |
id | pubmed-5790464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57904642018-02-08 BAFF and APRIL expression as an autoimmune signature of membranous nephropathy Han, Seung Seok Yang, Seung Hee Jo, Hyung Ah Oh, Yun Jung Park, Minkyoung Kim, Joo Young Lee, Hajeong Lee, Jung Pyo Lee, Sang-Ho Joo, Kwon Wook Lim, Chun Soo Kim, Yon Su Kim, Dong Ki Oncotarget Research Paper BACKGROUND: Based on the fact that B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) have a regulatory role in B cell biology, excessive levels of these cytokines can promote autoimmune pathogenesis. However, the expression and implication remain unresolved in cases of membranous nephropathy (MN). RESULTS: The plasma BAFF levels of the primary MN patients were higher than those of healthy controls but lower than those of secondary MN patients, whereas the APRIL levels were similar between the MN patients and healthy controls. The BAFF levels were higher in relapse cases, whereas the APRIL levels were higher in the patients who did not experience remission compared with the counterpart patients. The ectopic expression of BAFF and APRIL was observed in the glomeruli or circulating B cells of MN patients, and this high expression trend was similar to that of lupus patients. CONCLUSIONS: Expression profile of BAFF and APRIL in MN is similar to that of other autoimmune disease, which affects the kidney outcomes. METHODS: Plasma BAFF and APRIL levels were measured upon kidney biopsy in patients with primary (n = 89) and secondary MN (n = 13), and the results were compared with the levels in healthy controls (n = 111). The kidney outcomes (e.g., remission and relapse) were traced for the median of 3 years. Aberrant expression of the cytokines was evaluated in the kidney and circulating B cells using immunohistochemistry and flow cytometry analyses, respectively. Impact Journals LLC 2017-12-14 /pmc/articles/PMC5790464/ /pubmed/29423047 http://dx.doi.org/10.18632/oncotarget.23232 Text en Copyright: © 2018 Han et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Han, Seung Seok Yang, Seung Hee Jo, Hyung Ah Oh, Yun Jung Park, Minkyoung Kim, Joo Young Lee, Hajeong Lee, Jung Pyo Lee, Sang-Ho Joo, Kwon Wook Lim, Chun Soo Kim, Yon Su Kim, Dong Ki BAFF and APRIL expression as an autoimmune signature of membranous nephropathy |
title | BAFF and APRIL expression as an autoimmune signature of membranous nephropathy |
title_full | BAFF and APRIL expression as an autoimmune signature of membranous nephropathy |
title_fullStr | BAFF and APRIL expression as an autoimmune signature of membranous nephropathy |
title_full_unstemmed | BAFF and APRIL expression as an autoimmune signature of membranous nephropathy |
title_short | BAFF and APRIL expression as an autoimmune signature of membranous nephropathy |
title_sort | baff and april expression as an autoimmune signature of membranous nephropathy |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790464/ https://www.ncbi.nlm.nih.gov/pubmed/29423047 http://dx.doi.org/10.18632/oncotarget.23232 |
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