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Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review
Immunoglobulin A (IgA) nephropathy is a common autoimmune kidney disease. Accumulating studies showed that IgA nephropathy may be partially correlated with mucosal immune system dysfunction. Systemic corticosteroid treatment exerts an essential protective effect against renal deterioration in IgA ne...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846030/ https://www.ncbi.nlm.nih.gov/pubmed/36685528 http://dx.doi.org/10.3389/fimmu.2022.926517 |
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author | Liao, Jian Zhou, Yijing Xu, Xiuqin Huang, Ke Chen, Pengtao Wu, Yuhao Jin, Biao Hu, Qianlong Chen, Guanlin Zhao, Shankun |
author_facet | Liao, Jian Zhou, Yijing Xu, Xiuqin Huang, Ke Chen, Pengtao Wu, Yuhao Jin, Biao Hu, Qianlong Chen, Guanlin Zhao, Shankun |
author_sort | Liao, Jian |
collection | PubMed |
description | Immunoglobulin A (IgA) nephropathy is a common autoimmune kidney disease. Accumulating studies showed that IgA nephropathy may be partially correlated with mucosal immune system dysfunction. Systemic corticosteroid treatment exerts an essential protective effect against renal deterioration in IgA nephropathy. However, long-term use of corticosteroids may cause systemic side effects. The novel targeted-release formulation (TRF) of budesonide has been shown to deliver the drug to the distal ileum with the aim of minimizing adverse events for patients with IgA nephropathy. In this review, we have summarized all the current evidence of the effects of TRF-budesonide protecting against IgA nephropathy. Three randomized controlled trials (RCTs), one cohort, two case reports, and an ongoing Phase 3 trial (Part B, NCT03643965), were under comprehensive review. These included studies demonstrated that TRF-budesonide could remarkably reduce proteinuria, hematuria, and creatinine, as well as preserve renal function. The local immunosuppressive effects exhibited by TRF-budesonide may represent a novel and promising approach to treating IgA nephropathy. However, the current evidence was only derived from limited trials. Therefore, more well-designed RCTs are still warranted to validate the curable profile of TRF-budesonide in treating IgA nephropathy. |
format | Online Article Text |
id | pubmed-9846030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98460302023-01-19 Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review Liao, Jian Zhou, Yijing Xu, Xiuqin Huang, Ke Chen, Pengtao Wu, Yuhao Jin, Biao Hu, Qianlong Chen, Guanlin Zhao, Shankun Front Immunol Immunology Immunoglobulin A (IgA) nephropathy is a common autoimmune kidney disease. Accumulating studies showed that IgA nephropathy may be partially correlated with mucosal immune system dysfunction. Systemic corticosteroid treatment exerts an essential protective effect against renal deterioration in IgA nephropathy. However, long-term use of corticosteroids may cause systemic side effects. The novel targeted-release formulation (TRF) of budesonide has been shown to deliver the drug to the distal ileum with the aim of minimizing adverse events for patients with IgA nephropathy. In this review, we have summarized all the current evidence of the effects of TRF-budesonide protecting against IgA nephropathy. Three randomized controlled trials (RCTs), one cohort, two case reports, and an ongoing Phase 3 trial (Part B, NCT03643965), were under comprehensive review. These included studies demonstrated that TRF-budesonide could remarkably reduce proteinuria, hematuria, and creatinine, as well as preserve renal function. The local immunosuppressive effects exhibited by TRF-budesonide may represent a novel and promising approach to treating IgA nephropathy. However, the current evidence was only derived from limited trials. Therefore, more well-designed RCTs are still warranted to validate the curable profile of TRF-budesonide in treating IgA nephropathy. Frontiers Media S.A. 2023-01-04 /pmc/articles/PMC9846030/ /pubmed/36685528 http://dx.doi.org/10.3389/fimmu.2022.926517 Text en Copyright © 2023 Liao, Zhou, Xu, Huang, Chen, Wu, Jin, Hu, Chen and Zhao https://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 Liao, Jian Zhou, Yijing Xu, Xiuqin Huang, Ke Chen, Pengtao Wu, Yuhao Jin, Biao Hu, Qianlong Chen, Guanlin Zhao, Shankun Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review |
title | Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review |
title_full | Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review |
title_fullStr | Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review |
title_full_unstemmed | Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review |
title_short | Current knowledge of targeted-release budesonide in immunoglobulin A nephropathy: A comprehensive review |
title_sort | current knowledge of targeted-release budesonide in immunoglobulin a nephropathy: a comprehensive review |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846030/ https://www.ncbi.nlm.nih.gov/pubmed/36685528 http://dx.doi.org/10.3389/fimmu.2022.926517 |
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