Tumor-induced myeloid-derived suppressor cell subsets exert either inhibitory or stimulatory effects on distinct CD8+ T-cell activation events

Eur J Immunol. 2013 Nov;43(11):2930-42. doi: 10.1002/eji.201343349. Epub 2013 Aug 25.

Abstract

Tumor growth coincides with an accumulation of myeloid-derived suppressor cells (MDSCs), which exert immune suppression and which consist of two main subpopulations, known as monocytic (MO) CD11b(+) CD115(+) Ly6G(-) Ly6C(high) MDSCs and granulocytic CD11b(+) CD115(-) Ly6G(+) Ly6C(int) polymorphonuclear (PMN)-MDSCs. However, whether these distinct MDSC subsets hamper all aspects of early CD8(+) T-cell activation--including cytokine production, surface marker expression, survival, and cytotoxicity--is currently unclear. Here, employing an in vitro coculture system, we demonstrate that splenic MDSC subsets suppress antigen-driven CD8(+) T-cell proliferation, but differ in their dependency on IFN-γ, STAT-1, IRF-1, and NO to do so. Moreover, MO-MDSC and PMN-MDSCs diminish IL-2 levels, but only MO-MDSCs affect IL-2Rα (CD25) expression and STAT-5 signaling. Unexpectedly, however, both MDSC populations stimulate IFN-γ production by CD8(+) T cells on a per cell basis, illustrating that some T-cell activation characteristics are actually stimulated by MDSCs. Conversely, MO-MDSCs counteract the activation-induced change in CD44, CD62L, CD162, and granzyme B expression, while promoting CD69 and Fas upregulation. Together, these effects result in an altered CD8(+) T-cell adhesiveness to the extracellular matrix and selectins, sensitivity to FasL-mediated apoptosis, and cytotoxicity. Hence, MDSCs intricately influence different CD8(+) T-cell activation events in vitro, whereby some parameters are suppressed while others are stimulated.

Keywords: CD8+ T-cell activation; CD8+ T-cell suppression; Monocytic myeloid-derived suppressor cell (MO-MDSC); Nitric oxide; Polymorphonuclear MDSC (PMN-MDSC).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Antigens, Differentiation, T-Lymphocyte / biosynthesis
  • Antigens, Ly / metabolism
  • Apoptosis / immunology
  • CD11b Antigen / metabolism
  • CD8-Positive T-Lymphocytes / immunology*
  • Cell Adhesion / immunology
  • Cell Line
  • Cell Proliferation
  • Female
  • Granzymes / biosynthesis
  • Hyaluronan Receptors / biosynthesis
  • Interferon Regulatory Factor-1
  • Interferon-gamma / biosynthesis
  • Interleukin-2 / metabolism
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • L-Selectin / biosynthesis
  • Lectins, C-Type / biosynthesis
  • Lymphocyte Activation / immunology*
  • Membrane Glycoproteins / biosynthesis
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myeloid Cells / immunology*
  • Neoplasms / immunology*
  • Neutrophils / immunology
  • Nitric Oxide / metabolism
  • Receptor, Macrophage Colony-Stimulating Factor / metabolism
  • STAT1 Transcription Factor / metabolism
  • STAT5 Transcription Factor / metabolism
  • Signal Transduction / immunology
  • Up-Regulation
  • fas Receptor / biosynthesis

Substances

  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • Antigens, Ly
  • CD11b Antigen
  • CD69 antigen
  • Fas protein, mouse
  • Hyaluronan Receptors
  • Il2ra protein, mouse
  • Interferon Regulatory Factor-1
  • Interleukin-2
  • Interleukin-2 Receptor alpha Subunit
  • Lectins, C-Type
  • Ly-6C antigen, mouse
  • Ly6G antigen, mouse
  • Membrane Glycoproteins
  • P-selectin ligand protein
  • STAT1 Transcription Factor
  • STAT5 Transcription Factor
  • Stat1 protein, mouse
  • fas Receptor
  • L-Selectin
  • Nitric Oxide
  • Interferon-gamma
  • Receptor, Macrophage Colony-Stimulating Factor
  • Granzymes
  • Gzmb protein, mouse