Increased IL-17-producing CD4(+) T cells in patients with esophageal cancer

Cell Immunol. 2012;272(2):166-74. doi: 10.1016/j.cellimm.2011.10.015. Epub 2011 Oct 28.

Abstract

Increased interleukin-17 (IL-17)-producing Th (Th17) cells have been described in a variety of human carcinoma cases, however, the mechanism of Th17 cells' accumulation in a tumor microenvironment remains elusive. This study was designed to investigate whether Th17 cells were involved in the development of esophageal cancer. We found that the proportion of Th17 cells increased within the peripheral blood and tumor tissues of esophageal cancer patients. Furthermore, the proportion of circulating Th17 cells was higher in advanced esophageal cancer patients than that in early esophageal cancer patients. In addition, the Th17 cells differentiation-related cytokines (IL-23, IL-1β, and IL-6) and accumulation-related chemokines (CCL22 and CCL20) were present in a tumor microenvironment. Therefore, the findings may partly explain the cause for the increased proportion of Th17 cells and indicate a potential prognostic marker of Th17 cells in esophageal cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology
  • Cell Movement / genetics
  • Cell Movement / immunology*
  • Chemokine CCL20 / metabolism
  • Chemokine CCL22 / metabolism
  • Esophageal Neoplasms / immunology*
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / pathology
  • Female
  • Humans
  • Interleukin-17 / biosynthesis*
  • Interleukin-17 / immunology*
  • Interleukin-17 / metabolism
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Lymph Nodes / immunology
  • Lymph Nodes / metabolism
  • Male
  • Middle Aged
  • Neoplasm Staging / methods
  • Receptors, CCR4 / metabolism
  • Receptors, CCR6 / metabolism
  • Th17 Cells / immunology*
  • Th17 Cells / metabolism
  • Tumor Microenvironment / genetics
  • Tumor Microenvironment / immunology

Substances

  • CCL20 protein, human
  • CCL22 protein, human
  • CCR4 protein, human
  • CCR6 protein, human
  • Chemokine CCL20
  • Chemokine CCL22
  • Interleukin-17
  • Receptors, CCR4
  • Receptors, CCR6