CD4+ T-cell help in the tumor milieu is required for recruitment and cytolytic function of CD8+ T lymphocytes

Cancer Res. 2010 Nov 1;70(21):8368-77. doi: 10.1158/0008-5472.CAN-10-1322. Epub 2010 Oct 12.

Abstract

CD4 help for CD8(+) T lymphocytes prevents tolerance and promotes the survival of effector and memory CD8(+) T cells. Here, we describe additional helper functions that require CD4(+) T cells within the tumor environment. CD8(+) T-cell recruitment, proliferation, and effector function within the tumor were greatly enhanced by tumor-specific CD4(+) T cells. Recruitment of CD8(+) T cells was accelerated by IFN-γ-dependent production of chemokines. Production of interleukin-2 by tumor resident CD4(+) T cells enhanced CD8(+) T-cell proliferation and upregulated expression of granzyme B. These results highlight a novel role for tumor-specific CD4(+) T cells in promoting CD8(+) T-cell recruitment and cytolytic function, two previously unappreciated aspects of tumor-specific CD4 help.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / pathology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / pathology
  • Cell Proliferation
  • Cells, Cultured
  • Flow Cytometry
  • Granzymes / metabolism
  • Humans
  • Immunization
  • Interferon-gamma / metabolism
  • Interleukin-2 / metabolism
  • Lymph Nodes / metabolism
  • Lymph Nodes / pathology*
  • Mice
  • Mice, Transgenic
  • Neoplasms, Experimental / immunology*
  • Neoplasms, Experimental / pathology
  • Neoplasms, Experimental / therapy
  • Peptide Fragments / administration & dosage
  • Peptide Fragments / immunology
  • Rats

Substances

  • Interleukin-2
  • Peptide Fragments
  • Interferon-gamma
  • Granzymes