Foxp3-transduced polyclonal regulatory T cells protect against chronic renal injury from adriamycin

J Am Soc Nephrol. 2006 Mar;17(3):697-706. doi: 10.1681/ASN.2005090978. Epub 2006 Feb 8.

Abstract

Chronic proteinuric renal injury is a major cause of ESRD. Adriamycin nephropathy is a murine model of chronic proteinuric renal disease whereby chemical injury is followed by immune and structural changes that mimic human disease. Foxp3 is a gene that induces a regulatory T cell (Treg) phenotype. It was hypothesized that Foxp3-transduced Treg could protect against renal injury in Adriamycin nephropathy. CD4+ T cells were transduced with either a Foxp3-containing retrovirus or a control retrovirus. Foxp3-transduced T cells had a regulatory phenotype by functional and phenotypic assays. Adoptive transfer of Foxp3-transduced T cells protected against renal injury. Urinary protein excretion and serum creatinine were reduced (P<0.05), and there was significantly less glomerulosclerosis, tubular damage, and interstitial infiltrates (P<0.01). It is concluded that Foxp3-transduced Treg cells may have a therapeutic role in protecting against immune injury and disease progression in chronic proteinuric renal disease.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4-Positive T-Lymphocytes / drug effects
  • CD4-Positive T-Lymphocytes / physiology*
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Disease Models, Animal
  • Doxorubicin
  • Flow Cytometry
  • Forkhead Transcription Factors / pharmacology*
  • Immunohistochemistry
  • Kidney Failure, Chronic / chemically induced
  • Kidney Failure, Chronic / prevention & control*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Probability
  • Random Allocation
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sensitivity and Specificity
  • T-Lymphocytes, Regulatory / drug effects*
  • Transduction, Genetic

Substances

  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Doxorubicin