Cargando…

A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence

A PRoliferation-Inducing Ligand (APRIL), the thirteenth member of the tumor necrosis factor superfamily, plays a key role in the regulation of activated B cells, the survival of long-lived plasma cells, and immunoglobulin (Ig) isotype class switching. Several lines of evidence have implicated APRIL...

Descripción completa

Detalles Bibliográficos
Autores principales: Mathur, Mohit, Chan, Tak Mao, Oh, Kook-Hwan, Kooienga, Laura, Zhuo, Min, Pinto, Cibele S., Chacko, Bobby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650434/
https://www.ncbi.nlm.nih.gov/pubmed/37959392
http://dx.doi.org/10.3390/jcm12216927
_version_ 1785135780218273792
author Mathur, Mohit
Chan, Tak Mao
Oh, Kook-Hwan
Kooienga, Laura
Zhuo, Min
Pinto, Cibele S.
Chacko, Bobby
author_facet Mathur, Mohit
Chan, Tak Mao
Oh, Kook-Hwan
Kooienga, Laura
Zhuo, Min
Pinto, Cibele S.
Chacko, Bobby
author_sort Mathur, Mohit
collection PubMed
description A PRoliferation-Inducing Ligand (APRIL), the thirteenth member of the tumor necrosis factor superfamily, plays a key role in the regulation of activated B cells, the survival of long-lived plasma cells, and immunoglobulin (Ig) isotype class switching. Several lines of evidence have implicated APRIL in the pathogenesis of IgA nephropathy (IgAN). Globally, IgAN is the most common primary glomerulonephritis, and it can progress to end-stage kidney disease; yet, disease-modifying treatments for this condition have historically been lacking. The preliminary data in ongoing clinical trials indicate that APRIL inhibition can reduce proteinuria and slow the rate of kidney disease progression by acting at an upstream level in IgAN pathogenesis. In this review, we examine what is known about the physiologic roles of APRIL and evaluate the experimental and epidemiological evidence describing how these normal biologic processes are thought to be subverted in IgAN. The weight of the preclinical, clinical, and genetic data supporting a key role for APRIL in IgAN has galvanized pharmacologic research, and several anti-APRIL drug candidates have now entered clinical development for IgAN. Herein, we present an overview of the clinical results to date. Finally, we explore where more research and evidence are needed to transform potential therapies into clinical benefits for patients with IgAN.
format Online
Article
Text
id pubmed-10650434
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-106504342023-11-04 A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence Mathur, Mohit Chan, Tak Mao Oh, Kook-Hwan Kooienga, Laura Zhuo, Min Pinto, Cibele S. Chacko, Bobby J Clin Med Review A PRoliferation-Inducing Ligand (APRIL), the thirteenth member of the tumor necrosis factor superfamily, plays a key role in the regulation of activated B cells, the survival of long-lived plasma cells, and immunoglobulin (Ig) isotype class switching. Several lines of evidence have implicated APRIL in the pathogenesis of IgA nephropathy (IgAN). Globally, IgAN is the most common primary glomerulonephritis, and it can progress to end-stage kidney disease; yet, disease-modifying treatments for this condition have historically been lacking. The preliminary data in ongoing clinical trials indicate that APRIL inhibition can reduce proteinuria and slow the rate of kidney disease progression by acting at an upstream level in IgAN pathogenesis. In this review, we examine what is known about the physiologic roles of APRIL and evaluate the experimental and epidemiological evidence describing how these normal biologic processes are thought to be subverted in IgAN. The weight of the preclinical, clinical, and genetic data supporting a key role for APRIL in IgAN has galvanized pharmacologic research, and several anti-APRIL drug candidates have now entered clinical development for IgAN. Herein, we present an overview of the clinical results to date. Finally, we explore where more research and evidence are needed to transform potential therapies into clinical benefits for patients with IgAN. MDPI 2023-11-04 /pmc/articles/PMC10650434/ /pubmed/37959392 http://dx.doi.org/10.3390/jcm12216927 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mathur, Mohit
Chan, Tak Mao
Oh, Kook-Hwan
Kooienga, Laura
Zhuo, Min
Pinto, Cibele S.
Chacko, Bobby
A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence
title A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence
title_full A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence
title_fullStr A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence
title_full_unstemmed A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence
title_short A PRoliferation-Inducing Ligand (APRIL) in the Pathogenesis of Immunoglobulin A Nephropathy: A Review of the Evidence
title_sort proliferation-inducing ligand (april) in the pathogenesis of immunoglobulin a nephropathy: a review of the evidence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650434/
https://www.ncbi.nlm.nih.gov/pubmed/37959392
http://dx.doi.org/10.3390/jcm12216927
work_keys_str_mv AT mathurmohit aproliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT chantakmao aproliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT ohkookhwan aproliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT kooiengalaura aproliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT zhuomin aproliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT pintocibeles aproliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT chackobobby aproliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT mathurmohit proliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT chantakmao proliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT ohkookhwan proliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT kooiengalaura proliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT zhuomin proliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT pintocibeles proliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence
AT chackobobby proliferationinducingligandaprilinthepathogenesisofimmunoglobulinanephropathyareviewoftheevidence