Airway epithelial cell damage mediated by antigen-specific T cells: implications in lung allograft rejection

Hum Immunol. 2000 Oct;61(10):985-92. doi: 10.1016/s0198-8859(00)00175-0.

Abstract

The aim of this study is to assess the mechanisms associated with airway epithelial cell (AEC) injury, which may have implications in lung allograft rejection. Three AEC lines, KDI-650, Beas-2B and A549 were analyzed. Effect of cytokines on the expression of Fas, HLA class I, and HLA class II were assessed by flow cytometry. AEC-specific T cells were generated in vitro and assessed for lysis by (51)Cr release assay. HLA class I and Fas were expressed on all AEC lines. Beas-2B and A549 expressed low levels of class II compared with KDI-650, which lack this expression. Expression of HLA class II was augmented on KDI-650 and Beas-2B by IFN-gamma treatment. AEC-specific T cells generated in vitro were predominantly CD8(+) and lysed relevant AEC targets. Anti-HLA class I monoclonal antibodies inhibited the lysis of AEC by specific T cells while anti-Fas and anti-HLA class II monoclonal antibodies did not have any effect on the T cell induced lysis of AECs. AECs cultured with supernatant derived from T-cell cultures induced the expression of Fas, HLA class I, as well as HLA class II. These results suggest AEC damage is mediated by AEC-specific T cells primarily by the conventional HLA class I/peptide complex and TCR interaction. Further, the factors released by these T cells also induce the expression of Fas, as well as HLA class I and class II, which may have implications on the outcome of the immune response against AECs.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antibodies, Monoclonal / immunology
  • Cell Line
  • Culture Media
  • Cytokines / metabolism
  • Cytokines / pharmacology
  • Cytotoxicity, Immunologic
  • Epithelial Cells / cytology
  • Epithelial Cells / immunology
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Graft Rejection / immunology*
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class I / metabolism
  • Histocompatibility Antigens Class II / immunology
  • Histocompatibility Antigens Class II / metabolism
  • Humans
  • Lung / cytology
  • Lung / immunology*
  • Lung / pathology
  • Lung Transplantation / immunology*
  • Respiratory Mucosa / cytology
  • Respiratory Mucosa / immunology*
  • T-Lymphocytes, Cytotoxic / immunology*
  • T-Lymphocytes, Cytotoxic / metabolism
  • Transplantation, Homologous
  • fas Receptor / immunology
  • fas Receptor / metabolism

Substances

  • Antibodies, Monoclonal
  • Culture Media
  • Cytokines
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • fas Receptor