Lung function early after lung transplantation is correlated with the frequency of regulatory T cells

Surg Today. 2012 Feb;42(3):250-8. doi: 10.1007/s00595-011-0087-3. Epub 2011 Dec 17.

Abstract

Purposes: Outcomes following lung transplantation are limited by bronchiolitis obliterans syndrome (BOS). As the number of circulating regulatory T cells (Treg) is lower in lung recipients with BOS than in stable lung recipients, we hypothesized that Treg is also correlated with lung function in the early post-transplantation period.

Methods: This prospective study included 18 consecutive patients whose lung function parameters were recorded 3 weeks and 3 months after transplantation, between February and July 2007. Peripheral blood mononuclear cells were stained with anti-CD3, -CD4, -CD8, -CD19, -CD25, -CD28, -CD45RA, -CD45RO, -CD69, -CD127, -CTLA4, and -Foxp3 antibodies and FACS assays were performed. In addition, intracellular cytokines were stained for FACS.

Results: Treg-specific markers (Foxp3, CD127(lo), and CTLA4) in the CD25+ CD4+ population were correlated with both forced expiratory volume in 1 s and forced vital capacity. Th1-cytokine secretion was more dominant in CD4+ CD25+ T cells than in CD4+ CD25- T cells. In contrast, Th2 and Treg cytokine secretion was the dominant response in stable recipients.

Conclusions: The frequency of Treg cells was positively correlated with good lung function in the early period after lung transplantation.

MeSH terms

  • Acute-Phase Reaction / etiology
  • Acute-Phase Reaction / immunology
  • Adult
  • Antigens, CD / blood*
  • Biomarkers / blood
  • Bronchiolitis Obliterans / etiology
  • Bronchiolitis Obliterans / immunology
  • Cytokines / blood*
  • Female
  • Flow Cytometry
  • Forced Expiratory Volume
  • Forkhead Transcription Factors / blood*
  • Graft Rejection / immunology
  • Humans
  • Leukocytes, Mononuclear / metabolism
  • Lung Transplantation / immunology*
  • Lung Transplantation / physiology
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Postoperative Complications / immunology
  • Primary Graft Dysfunction / immunology
  • Prospective Studies
  • T-Lymphocytes, Regulatory / metabolism*
  • Vital Capacity

Substances

  • Antigens, CD
  • Biomarkers
  • Cytokines
  • FOXP3 protein, human
  • Forkhead Transcription Factors