Transcription Factors in the Pathogenesis of Lupus Nephritis and Their Targeted Therapy

Author:

Shao Kasey M.1,Shao Wen-Hai2ORCID

Affiliation:

1. Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA

2. Division of Rheumatology, Allergy and Immunology, Department of Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA

Abstract

Systemic lupus erythematosus (SLE) is a prototype inflammatory autoimmune disease, characterized by breakdown of immunotolerance to self-antigens. Renal involvement, known as lupus nephritis (LN), is one of the leading causes of morbidity and a significant contributor to mortality in SLE. Despite current pathophysiological advances, further studies are needed to fully understand complex mechanisms underlying the development and progression of LN. Transcription factors (TFs) are proteins that regulate the expression of genes and play a crucial role in the development and progression of LN. The mechanisms of TF promoting or inhibiting gene expression are complex, and studies have just begun to reveal the pathological roles of TFs in LN. Understanding TFs in the pathogenesis of LN can provide valuable insights into this disease’s mechanisms and potentially lead to the development of targeted therapies for its management. This review will focus on recent findings on TFs in the pathogenesis of LN and newly developed TF-targeted therapy in renal inflammation.

Funder

University of Cincinnati’s College of Medicine Bridge Fund

Department of Internal Medicine Senior Faculty Award

Publisher

MDPI AG

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