Tumour-loaded α-type 1-polarized dendritic cells from patients with chronic lymphocytic leukaemia produce a superior NK-, NKT- and CD8+ T cell-attracting chemokine profile

Scand J Immunol. 2011 Sep;74(3):318-326. doi: 10.1111/j.1365-3083.2011.02580.x.

Abstract

Tumour-loaded dendritic cells (DCs) from patients with chronic lymphocytic leukaemia (CLL) matured using an α-type 1-polarized DC cocktail (IL-1β/TNF-α/IFN-α/IFN-γ/poly-I:C;αDC1) were recently shown to induce more functional CD8(+) T cells against autologous tumour cells in vitro than DCs matured with the 'standard' cocktail (IL-1β/TNF-α/IL-6/PGE(2) ;PGE(2) DCs). However, the ability of vaccine DCs to induce a type 1-polarized immune response in vivo probably relies on additional features, including their ability to induce a CXCR3-dependent recruitment of NK cells into vaccine-draining lymph nodes. Moreover, their guiding of rare tumour-specific CD8(+) T cells to sites of DC-CD4(+) T cell interactions by secretion of CCL3 and CCL4 is needed. We therefore analysed the chemokine profile and the lymphocyte-attracting ability in vitro of monocyte-derived PGE(2) DCs and αDC1s from patients with CLL. αDC1s produced much higher levels of CXCR3 ligands (CXCL9/CXCL10/CXCL11) than PGE(2) DCs. Functional studies further demonstrated that αDC1s were superior recruiters of both NK and NKT cells. Moreover, αDC1s produced higher levels of CCL3/CCL4 upon CD40 ligation. These findings suggest that functional αDC1s, derived from patients with CLL, produce a desirable NK-, NKT- and CD8(+) T cell-attracting chemokine profile which may favour a guided and Th1-deviated priming of CD8(+) T cells, supporting the idea that αDC1-based vaccines have a higher immunotherapeutic potential than PGE(2) DCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD40 Antigens / immunology
  • CD8-Positive T-Lymphocytes / immunology*
  • Cell Movement / immunology
  • Cell Polarity
  • Chemokine CCL3 / biosynthesis
  • Chemokine CCL3 / immunology
  • Chemokine CCL4 / biosynthesis
  • Chemokine CCL4 / immunology
  • Chemokines / biosynthesis
  • Chemokines / immunology*
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Humans
  • Killer Cells, Natural / immunology*
  • Leukemia, Lymphocytic, Chronic, B-Cell / immunology*
  • Lymphocyte Activation
  • Natural Killer T-Cells / immunology*
  • Receptors, CXCR3 / biosynthesis
  • Receptors, CXCR3 / immunology

Substances

  • CCL3 protein, human
  • CCL4 protein, human
  • CD40 Antigens
  • CXCR3 protein, human
  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokines
  • Receptors, CXCR3