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Refractory lupus nephritis: When, why and how to treat.

Accepted version
Peer-reviewed

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Type

Article

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Authors

Kronbichler, Andreas  ORCID logo  https://orcid.org/0000-0002-2945-2946
Brezina, Biljana 
Gauckler, Philipp 
Quintana, Luis F 
Jayne, David RW 

Abstract

Refractory lupus nephritis indicates an inadequate response to lupus nephritis therapy. It implies persisting or worsening disease activity despite therapy, but the definition is complicated by the parameters of response, proteinuria and renal function, that do not discriminate clearly between activity and irreversible damage. Understanding the causes of refractory disease and developing treatment strategies is important because these patients are more likely to develop poor outcomes, especially end stage renal disease. This review explores current concepts and definitions of refractory disease and summarises treatment approaches that have been used in observational cohort studies and case series. We highlight the importance of optimising adherence to the prescribed immunosuppressive and supportive measures and avoidance of diagnostic delay. Treatment options include higher dose glucocorticoid, switching between cyclophosphamide and mycophenolate acid derivates, or addition of rituximab, the latter potentially in combination with belimumab. Less evidence supports extracorporeal treatment (plasma exchange or immunoadsorption), calcineurin inhibitors (cyclosporine A or tacrolimus), intravenous immunoglobulin and stem cell transplantation. Improvements in understanding what refractory disease is and how definitions can be integrated into treatment pathways has the potential to enhance lupus nephritis outcomes.

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Keywords

Bortezomib, Immunoadsorption, Lupus nephritis, Multi-target, Refractory, Rituximab, Transplantation, Treatment, Delayed Diagnosis, Humans, Immunosuppressive Agents, Lupus Nephritis, Mycophenolic Acid, Observational Studies as Topic, Remission Induction, Time Factors, Treatment Failure

Journal Title

Autoimmun Rev

Conference Name

Journal ISSN

1568-9972
1873-0183

Volume Title

18

Publisher

Elsevier BV