Absence of the CD1 molecule up-regulates antitumor activity induced by CpG oligodeoxynucleotides in mice

J Immunol. 2002 Jul 1;169(1):151-8. doi: 10.4049/jimmunol.169.1.151.

Abstract

The role of NKT cells on antitumor activity of CpG oligodeoxynucleotides (ODNs) was evaluated by peritumoral injections of CpG-ODNs in s.c. melanoma-bearing mice of strains differing in the number of NKT cells (athymic nude mice, recombination-activating gene(-/-)/transgenic V(alpha)14/Vbeta8.2 mice that generate NKT cells; J(alpha)281(-/-) mice and CD1(-/-) mice, which both have a strongly reduced number of NKT cells; and C57BL/6 wild-type mice). Tumor growth was significantly inhibited in strains enriched or depleted of NKT cells. The two murine strains having a reduced number of NKT cells differed significantly in the CpG-dependent tumor growth inhibition: in J(alpha)281(-/-) mice this inhibition was superimposable to that observed in C57BL/6 mice, while in CD1(-/-) mice the inhibition was dramatic. The increased tumor inhibition in CD1(-/-) correlated with a significantly higher ratio of IFN-gamma-IL-4 production in response to CpG as compared with C57BL/6 and J(alpha)281(-/-) mice. Experiments in which preparations of APCs and lymphocytes of the three strains were mixed showed that in the presence of APCs not expressing CD1, the production of CpG-ODN-induced type 1 cytokines was higher. Phenotype analysis of IFN-gamma- and IL-4-producing cells revealed that the differences between CD1(-/-) and C57BL/6 in the production of these two cytokines were mainly due to CD3(+) T lymphocytes. These data point to a regulatory role for the CD1 molecule in antitumor activity induced by danger signals, independently of V(alpha)14 NKT cells. The identification of a CD1-dependent suppressive subpopulation(s) might have important implications for the study of tolerance in the context of cancer, autoimmunity, and transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / administration & dosage*
  • Animals
  • Antigen-Presenting Cells / immunology
  • Antigens, CD1 / genetics*
  • Antigens, CD1 / physiology
  • CpG Islands / immunology*
  • Cytokines / biosynthesis
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / genetics
  • Homeodomain Proteins / genetics
  • Immunophenotyping
  • Injections, Intralesional
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / metabolism
  • Interleukin-4 / metabolism
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Melanoma, Experimental / immunology
  • Melanoma, Experimental / prevention & control*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Nude
  • Mice, Transgenic
  • Neoplasm Transplantation
  • Oligodeoxyribonucleotides / administration & dosage*
  • Receptors, Antigen, T-Cell, alpha-beta / deficiency
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • Up-Regulation / genetics*
  • Up-Regulation / immunology*

Substances

  • Adjuvants, Immunologic
  • Antigens, CD1
  • CPG-oligonucleotide
  • Cytokines
  • DNA-Binding Proteins
  • Homeodomain Proteins
  • Oligodeoxyribonucleotides
  • Rag2 protein, mouse
  • Receptors, Antigen, T-Cell, alpha-beta
  • V(D)J recombination activating protein 2
  • RAG-1 protein
  • Interleukin-4
  • Interferon-gamma