PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
October 11, 2025Frontiers in Immunology7 citationsOpen Access

Breaking the cycle: immune complexes, complement activation, and novel immunotherapies in lupus nephritis

View Full Paper
CDChuan DongMWMing‐Shiou WuHLHaonan Liu

Key Points

  • Lupus nephritis is characterized by immune complex deposition and complement activation, leading to kidney damage.
  • Recent biomarkers like NGAL and TWEAK enhance noninvasive monitoring of disease activity and treatment response.
  • Targeted immunotherapies such as belimumab significantly improve outcomes by modulating B-cell function.
  • Emerging therapies demonstrate promise in treating refractory lupus nephritis, potentially improving long-term prognosis.

Abstract

Lupus nephritis (LN), a severe manifestation of systemic lupus erythematosus (SLE), is driven by immune complex deposition and complement activation, resulting in glomerular inflammation and podocyte injury. Beyond being passive targets, podocytes actively modulate renal immunity through cytokine secretion and antigen presentation. Recent advances in urinary biomarkers such as NGAL, TWEAK, and MCP-1 and composite indices like the Renal Activity Index for Lupus (RAIL) offer dynamic and noninvasive monitoring of disease activity. Immunotherapy has transitioned from nonspecific immunosuppression to targeted biologics, with agents such as belimumab and telitacicept improving outcomes by modulating B-cell function. Additionally, emerging therapies including bortezomib and daratumumab demonstrate efficacy in refractory LN through plasma cell depletion. This review summarizes current immunological insights, biomarker innovations, and immunotherapy strategy to support precision medicine and improve long-term renal prognosis in LN.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Dong et al. (2025) studied this question.

synapsesocial.com/papers/68e9b1c9ba7d64b6fc1328a3https://doi.org/10.3389/fimmu.2025.1624850
Ask AI
Helpful
Bookmark
Share
View Full Paper