T lymphocyte subsets and cytokine production by graft-infiltrating cells in FSGS recurrence post-transplantation

Nephrol Dial Transplant. 1999 Mar;14(3):713-6. doi: 10.1093/ndt/14.3.713.

Abstract

Background: Focal segmental glomerulosclerosis (FSGS) aetiology remains undefined although a derangement of lymphocytes and monocytes macrophages, at least, has been strongly suspected. We report the graft-infiltrating phenotypes and their cytokine production in a case of FSGS recurrence post-transplantation.

Methods: The kidney transplant recipient suffered immediate FSGS recurrence. Aspiration biopsies were done at the first and second week post-surgery and were analysed by flow cytometry. The cytokine analysis was done on aspiration sample culture supernatants and serum by enzyme-linked immunosorbent assay.

Results: High expression of CD3CD69, CD3CD71 and CD4CD29 was found on infiltrating lymphocytes. Biopsy cultures pointed to a Th0/Th1 pattern of cytokine production as well as significant synthesis of transforming growth factor-beta1. Interestingly, monocyte chemokines were absent.

Conclusion: We report evidence of intragraft lymphocyte activation in the early days of FSGS recurrence. Aspiration biopsy cultures showed failure of cyclosporin A to inhibit interleukin-2 (IL-2) production by infiltrating lymphocytes. If our findings are confirmed in similar patients, a trial with anti-IL-2-receptor antibody could be warranted.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antigens, CD / analysis
  • Cytokines / biosynthesis*
  • Flow Cytometry
  • Glomerulosclerosis, Focal Segmental / etiology
  • Glomerulosclerosis, Focal Segmental / immunology*
  • Humans
  • Kidney Transplantation / adverse effects*
  • Lymphocyte Activation
  • Male
  • Recurrence
  • T-Lymphocyte Subsets / immunology*

Substances

  • Antigens, CD
  • Cytokines