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Review Article

Animal models of lupus nephritis: the past, present and a future outlook

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Article: 2319203 | Received 10 Dec 2023, Accepted 11 Feb 2024, Published online: 13 Mar 2024
 

Abstract

Lupus nephritis (LN) is the most severe end-organ pathology in Systemic Lupus Erythematosus (SLE). Research has enhanced our understanding of immune effectors and inflammatory pathways in LN. However, even with the best available therapy, the rate of complete remission for proliferative LN remains below 50%. A deeper understanding of the resistance or susceptibility of renal cells to injury during the progression of SLE is critical for identifying new targets and developing effective long-term therapies. The complex and heterogeneous nature of LN, combined with the limitations of clinical research, make it challenging to investigate the aetiology of this disease directly in patients. Hence, multiple murine models resembling SLE-driven nephritis are utilised to dissect LN's cellular and genetic mechanisms, identify therapeutic targets, and screen novel compounds. This review discusses commonly used spontaneous and inducible mouse models that have provided insights into pathogenic mechanisms and long-term maintenance therapies in LN.

Disclosure statement

The authors have declared that no conflict of interest exists.

Additional information

Funding

Supported by grants from Vifor Pharma (P0213104, P0226952) and NIH (RO1DK136011) to Yogesh Scindia and Laurence Morel.