Inhibition of T Cell Alloreactivity by Bronchial Epithelium Is Impaired in Lung Transplant Recipients, Through Pathways Involving TGF-β, IL-10 and HLA-G

Transplantation. 2017 Sep;101(9):2192-2199. doi: 10.1097/TP.0000000000001553.

Abstract

Background: Bronchiolitis obliterans syndrome (BOS) after lung transplantation (LTx) results from bronchial epithelial cell (BECs) damages, thought to be orchestrated by T cells primed by antigen-presenting cell presenting alloantigens. In this cell cross-talk, BECs are also suspected to play a pivotal immunosuppressive role in T cell alloreactivity. We studied the immunomodulating role of BECs in a human ex vivo model of allogeneic T cell response, both in healthy subjects and LTx recipients.

Methods: BECs from 35 LTx recipients (n = 22 stable, n = 13 BOS) and healthy controls (n = 25) were cultured as primary cell cultures. Their inhibitory capacities through the involvement of tolerogenic molecules (HLA-G, TGF-β, and IL-10) were tested on a mixed lymphocyte reaction between antigen-presenting cells and recipient T cells.

Results: Control BECs inhibited T cell alloproliferation by a mean of 53 ± 7%. This inhibitory effect of BECs was significantly reduced in the stable LTx group (24 ± 8%, P = 0.009), but not in the BOS TxP group (53 ± 10%, P = 0.97). Neutralization of HLA-G, TGF-β, and IL-10 partially restored T cell alloproliferation, arguing for their involvement in the immunosuppressive effect of BECs. BECs culture supernatant from stable LTx patients with impaired BEC properties showed a skewed Th2-type secretion profile (high IL-4/IFN-γ ratio).

Conclusions: The inhibitory properties of BECs are dysregulated in stable LTx recipients, which could suggest their instrumental role in the initiation of BOS process and potential targeted therapies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bronchiolitis Obliterans / etiology*
  • Bronchiolitis Obliterans / immunology
  • Bronchiolitis Obliterans / metabolism
  • Bronchiolitis Obliterans / pathology
  • Case-Control Studies
  • Cell Proliferation
  • Cells, Cultured
  • Coculture Techniques
  • Epithelial Cells / immunology
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Female
  • HLA-G Antigens / immunology
  • HLA-G Antigens / metabolism*
  • Humans
  • Immunity, Mucosal*
  • Interleukin-10 / immunology
  • Interleukin-10 / metabolism*
  • Lung Transplantation / adverse effects*
  • Lymphocyte Activation
  • Lymphocyte Culture Test, Mixed
  • Male
  • Middle Aged
  • Primary Cell Culture
  • Prospective Studies
  • Respiratory Mucosa / immunology
  • Respiratory Mucosa / metabolism*
  • Respiratory Mucosa / pathology
  • Signal Transduction
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes / pathology
  • Transforming Growth Factor beta / immunology
  • Transforming Growth Factor beta / metabolism*
  • Treatment Outcome

Substances

  • HLA-G Antigens
  • IL10 protein, human
  • Transforming Growth Factor beta
  • Interleukin-10