Targeting B cells in immune-mediated kidney diseases: conclusions from a Kidney Disease: Improving Global Outcomes

Jürgen Floege1, Isabelle M Ayoub2, Silke R Brix3

  • 1Department of Nephrology & Rheumatology, University Hospital, Rheinisch-Westfälische Technische Hochschule (RWTH) Aachen, Aachen, Germany.

Kidney International
|April 25, 2026
PubMed

Insights

B cell therapies show varied success in glomerular diseases. Research is needed to optimize treatments and biomarkers for conditions like IgA nephropathy and lupus nephritis.

Area of Science:

  • Nephrology
  • Immunology
  • Pharmacology

Background:

  • B cell depletion and modulation are emerging treatments for immune-mediated glomerular diseases.
  • Current therapies exhibit variable efficacy and safety profiles across different kidney conditions.

Purpose of the Study:

  • To review evidence on B cell-targeted therapies for glomerular diseases.
  • To identify knowledge gaps and research needs for optimizing these treatments.

Main Methods:

  • Convened a KDIGO Controversies Conference in June 2025.
  • Reviewed current evidence on B cell therapies in IgA nephropathy, membranous nephropathy, podocytopathies, lupus nephritis, and ANCA-associated glomerulonephritis.

Main Results:

  • Anti-CD20 therapy shows limited efficacy in IgA nephropathy but is first-line for membranous nephropathy.
  • Rituximab is effective for lupus nephritis and ANCA-associated glomerulonephritis; CAR T-cell therapy shows promise for lupus nephritis.
  • Safety profiles differ, with CAR T-cell therapy requiring careful patient selection due to potential adverse events.

Conclusions:

  • B cell therapy effectiveness and safety vary significantly across glomerular diseases.
  • Critical research needs include biomarker validation, treatment protocol optimization, and determining optimal therapy duration.

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