Recurrent Glomerular Disease after Kidney Transplantation: Diagnostic and Management Dilemmas

Clin J Am Soc Nephrol. 2021 Nov;16(11):1730-1742. doi: 10.2215/CJN.00280121. Epub 2021 Oct 22.

Abstract

Recurrent glomerular disease after kidney transplant remains an important cause of allograft failure. Many of the different entities post-transplant still suffer from incomplete knowledge on pathophysiology, and therefore lack targeted and effective therapies. In this review, we focus on specific clinical dilemmas encountered by physicians in managing recurrent glomerular disease by highlighting new insights into the understanding and treatment of post-transplant focal segmental glomerulosclerosis, membranous nephropathy, atypical hemolytic uremic syndrome, C3 glomerulopathy, amyloid light-chain (AL) amyloidosis, and IgA nephropathy.

Keywords: allograft failure; glomerular disease; glomerulonephritis; kidney transplantation; kidney transplantation series; recurrent glomerular disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloidosis / complications
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Atypical Hemolytic Uremic Syndrome / diagnosis
  • Atypical Hemolytic Uremic Syndrome / genetics
  • Atypical Hemolytic Uremic Syndrome / therapy*
  • Autoantibodies / blood
  • Complement C3 / metabolism
  • Complement Inactivating Agents / therapeutic use
  • Genetic Testing
  • Glomerulonephritis / diagnosis*
  • Glomerulonephritis / genetics
  • Glomerulonephritis / pathology
  • Glomerulonephritis / therapy*
  • Humans
  • Kidney Failure, Chronic / etiology
  • Kidney Failure, Chronic / surgery
  • Kidney Transplantation*
  • Nephrectomy
  • Plasmapheresis
  • Predictive Value of Tests
  • Receptors, Phospholipase A2 / immunology
  • Recurrence
  • Risk Factors

Substances

  • Antibodies, Monoclonal, Humanized
  • Autoantibodies
  • C3 protein, human
  • Complement C3
  • Complement Inactivating Agents
  • PLA2R1 protein, human
  • Receptors, Phospholipase A2
  • eculizumab