The phenomenon of focal segmental glomerulosclerosis post-transplantation--a one-hit wonder?

Research output: Contribution to journalArticle (Academic Journal)peer-review

7 Citations (Scopus)

Abstract

Steroid resistant nephrotic syndrome (SRNS), otherwise termed focal segmental glomerulosclerosis (FSGS) is one of the most difficult conditions to manage for the nephrologist, particularly when the disease recurs post-transplantation. It is also fascinating from the biological perspective, as the non-genetic form appears highly likely to be caused by a disorder of circulating plasma, leading to the search for the elusive 'plasma factor' over several decades of research. Many hypotheses have been proposed and tested, and to date none have yet passed the test of clinical utility. The search appears to be narrowing, aided by landmark discoveries in the molecular properties of the glomerular filtration barrier, and improved experimental tools. Therapeutically we are also more able to target specific molecules, for example by monoclonal antibody treatments. In this context, the report of the effects of TNF-α on podocytes is instructive. This tells us that this cytokine could have directly deleterious effects on podocytes in vivo, and that this effect can be targeted clinically, potentially halting or reversing the disease process. As with all thought provoking research, this raises several interesting questions. Is TNF-α the elusive 'factor' or is it one of several? Is it directly affecting the glomerular filtration barrier, or modulating the immune response? And could this technique be used as a cell based assay for disease activity? This report adds to the growing list of candidates that need to be tested in a wider population of well phenotyped patients with SRNS. [corrected].

Original languageEnglish
Pages (from-to)2163-6
Number of pages4
JournalPediatric Nephrology
Volume27
Issue number12
DOIs
Publication statusPublished - Dec 2012

Keywords

  • Female
  • Glomerulosclerosis, Focal Segmental
  • Humans
  • Integrin beta3
  • Podocytes
  • Tumor Necrosis Factor-alpha

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