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BioMed research international

Publication date: 2016-01-01
Volume: 2016
Publisher: Hindawi Limited

Author:

Kronbichler, Andreas
Leierer, Johannes ; Oh, Jun ; Meijers, Björn ; Shin, Jae Il

Keywords:

Science & Technology, Life Sciences & Biomedicine, Biotechnology & Applied Microbiology, Medicine, Research & Experimental, Research & Experimental Medicine, MINIMAL CHANGE DISEASE, NEPHROTIC SYNDROME, LYMPHOCYTE SUBPOPULATIONS, RITUXIMAB TREATMENT, STEROID-RESISTANT, CELLS, EXPRESSION, CHILDREN, ADALIMUMAB, INDUCTION, Disease Progression, Glomerulosclerosis, Focal Segmental, Humans, Immunosuppressive Agents, Interleukin-1beta, Kidney Failure, Chronic, Kidney Glomerulus, Kidney Transplantation, Transforming Growth Factor beta1, Tumor Necrosis Factor-alpha, 06 Biological Sciences, 08 Information and Computing Sciences, 10 Technology

Abstract:

Focal segmental glomerulosclerosis is a histological pattern on renal biopsy caused by diverse mechanisms. In its primary form, a circulatory factor is implicated in disease onset and recurrence. The natural history of primary FSGS is unpredictable, since some patients are unresponsive towards immunosuppressive measures. Immunologic changes, leading to a proinflammatory or profibrotic milieu, have been implicated in disease progression, namely, glomerular scarring, eventually leading to end-stage renal disease. Among these, interleukin-1ß, tumor-necrosis factor-α (TNF-α), and transforming growth factor-ß1 (TGF-ß1) have emerged as important factors. Translating these findings into clinical practice dampened the enthusiasm, since both TNF-α and TGF-ß1 blockade failed to achieve significant control of the disease. More recently, a role of the complement system has been demonstrated which in fact may be another attractive target in clinical practice. Rituximab, blocking CD20-bearing cells, demonstrated conflicting data regarding efficacy in FSGS. Finally, the T-cell costimulating molecule B7-1 (CD80) is implicated in development of proteinuria in general. Blockade of this target demonstrated significant benefits in a small cohort of resistant patients. Taken together, this review focuses on immunology of FSGS, attributable to either the disease or progression, and discusses novel therapeutic approaches aiming at targeting immunologic factors.