Lupus nephritis: new progress in diagnosis and treatment

J Autoimmun. 2022 Oct:132:102871. doi: 10.1016/j.jaut.2022.102871. Epub 2022 Aug 20.

Abstract

Systemic lupus erythematosus (SLE) is a chronic multifactorial autoimmune disease that affects many organs, including the kidney. Lupus nephritis (LN) is a common manifestation characterized by heterogeneous clinical and histopathological findings, and often associates with poor prognosis. The diagnosis and treatment of LN is challenging, depending largely on renal biopsy, and there is no reliable non-invasive LN biomarker. Up to now, the complete remission rate of LN is only 20%∼30% after receiving six months of standard treatment, which is far from satisfactory. Moreover, adverse reactions to immunosuppressants, especially glucocorticoids, further compromise the prognosis of LN. Biological reagents targetting autoimmune responses and inflammatory pathways, bring hope to the treatment of intractable lupus. The European Renal Association-European Dialysis and Transplant Association (EULAR/ERA-EDTA) and KDIGO (Kidney Disease: Improving Global Outcomes) have been working on and launched the recommendations for the management of LN. In this review, we update our knowledge in the pathogenesis, diagnosis, and management of LN and prospect for the future potential targets in the management of LN.

Keywords: Biologics; Diagnosis; Lupus nephritis; Treatment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoimmunity
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Kidney
  • Lupus Erythematosus, Systemic*
  • Lupus Nephritis* / diagnosis
  • Lupus Nephritis* / therapy

Substances

  • Immunosuppressive Agents