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Urinary monocyte chemoattractant protein-1 in renal disease

Journal

CLINICA CHIMICA ACTA
Volume 412, Issue 23-24, Pages 2022-2030

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cca.2011.07.023

Keywords

Urinary biomarker; Chemokine; Glomerulonephritis; Acute kidney injury; Polycystic kidney disease; Diabetic nephropathy

Funding

  1. Roche Palo Alto
  2. AstraZeneca Limited
  3. Cyclacel Limited
  4. Baxter Biosciences
  5. Swiss National Science Foundation
  6. Novartis Foundation
  7. Medical Research Council
  8. Wellcome Trust
  9. Imperial College Healthcare Charity
  10. National Institute for Health Research (NIHR) Biomedical Research Centre

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Monocyte chemoattractant protein-1 (MCP-1/CCL2) has a critical role in the development of various renal diseases. Data from disease specific experimental animal models and clinical studies confirm that MCP-1 plays an important part in the pathogenesis of renal diseases. The action of MCP-1 in these studies has been shown to be more complex than the traditional concept of monocyte/macrophage recruitment to the inflammatory site. MCP-1 is expressed in renal tissues and it is detectable in urine of patients with a variety of renal diseases. Measurement of urinary levels of MCP-1 can provide valuable information not only for the diagnosis of active renal disease, but also for monitoring of response to therapy. Urinary MCP-1 measurement can provide help with evaluation of the prognosis in various renal diseases. Furthermore, selective targeting of MCP-1 could be an effective treatment in suppressing a number of renal diseases as blocking MCP-1 has already been shown to ameliorate renal diseases in experimental animal models. The advantage of measuring urinary MCP-1 rather than the conventional markers must now be validated using a larger cohort of patients in different renal diseases. Also the therapeutic potential of MCP-1 targeting agents needs to be investigated in clinical studies. Crown Copyright (C) 2011 Published by Elsevier B.V. All rights reserved.

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