Alternatively activated macrophages inhibit T-cell proliferation by Stat6-dependent expression of PD-L2

Blood. 2010 Oct 28;116(17):3311-20. doi: 10.1182/blood-2010-02-271981. Epub 2010 Jul 12.

Abstract

Alternatively activated macrophages (AAM) accumulate in tissues during Th2-associated immune responses like helminth infections and allergic disorders. These cells differentiate in response to interleukin 4 (IL-4)/IL-13-mediated activation of Stat6 and possess potent inhibitory activity against T cells. The molecular mechanism that leads to T-cell suppression remains unclear and could involve soluble factors or inhibitory ligands. Microarray analysis revealed that the inhibitory ligand, programmed death ligand 2 (PD-L2) was strongly induced by IL-4 in macrophages from wild-type but not Stat6-deficient mice. PD-L2 expression correlated with other established markers for AAM-like Relm-α/Fizz1, arginase1, or Ym1 and thereby serves as useful surface marker to identify and isolate AAM from tissues. Antibodies against PD-L2 blocked the inhibitory activity of AAM and retroviral expression of PD-L2 in macrophages from Stat6(-/-) mice was sufficient to inhibit T-cell proliferation, which demonstrates that PD-L2 mediates potent and nonredundant inhibition of T cells independently of other Stat6-regulated genes. Infection of conditional IL-4/IL-13-deficient mice with the helminth Nippostrongylus brasiliensis further showed that PD-L2 expression was dependent on IL-4/IL-13 from Th2 cells. In vivo blockade of PD-L2 during N brasiliensis infection caused an enhanced Th2 response in the lung, indicating that AAM inhibit Th2 cells by expression of PD-L2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B7-1 Antigen / genetics
  • B7-1 Antigen / immunology
  • B7-H1 Antigen
  • Cell Proliferation
  • Cells, Cultured
  • Gene Deletion
  • Gene Expression Regulation
  • Interleukin-4 / immunology*
  • Lung / immunology
  • Lung / parasitology
  • Macrophage Activation
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / parasitology*
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology
  • Mice
  • Mice, Inbred BALB C
  • Nippostrongylus / immunology*
  • Peptides / genetics
  • Peptides / immunology*
  • Programmed Cell Death 1 Ligand 2 Protein
  • STAT6 Transcription Factor / genetics
  • STAT6 Transcription Factor / immunology*
  • T-Lymphocytes / cytology*
  • Th2 Cells / immunology

Substances

  • B7-1 Antigen
  • B7-H1 Antigen
  • Cd274 protein, mouse
  • Membrane Glycoproteins
  • Pdcd1lg2 protein, mouse
  • Peptides
  • Programmed Cell Death 1 Ligand 2 Protein
  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Interleukin-4