Dendritic cells (DCs) are the quintessential antigen-presenting cells of the human immune system and play a prime role in coordinating innate and adaptive immune responses, explaining the strong and still growing interest in their application for cancer immunotherapy. Much current research in the field of DC-based immunotherapy focuses on optimizing the culture conditions for in vitro DC generation in order to assure that DCs with the best possible immunogenic qualities are being used for immunotherapy. In this context, monocyte-derived DCs that are alternatively induced by interleukin-15 (IL-15 DCs) have attracted recent attention due to their superior immunostimulatory characteristics. In this study, we show that IL-15 DCs, in addition to potent tumor antigen-presenting function, possess tumoricidal potential and thus qualify for the designation of killer DCs. Notwithstanding marked expression of the natural killer (NK) cell marker CD56 on a subset of IL-15 DCs, we found no evidence of a further phenotypic overlap between IL-15 DCs and NK cells. Allostimulation and antigen presentation assays confirmed that IL-15 DCs should be regarded as bona fide myeloid DCs not only from the phenotypic but also from the functional point of view. Concerning their cytotoxic activity, we demonstrate that IL-15 DCs are able to induce apoptotic cell death of the human K562 tumor cell line, while sparing tumor antigen-specific T cells. The cytotoxicity of IL-15 DCs is predominantly mediated by granzyme B and, to a small extent, by tumor necrosis factor-α (TNF-α)-related apoptosis-inducing ligand (TRAIL) but is independent of perforin, Fas ligand and TNF-α. In conclusion, our data provide evidence of a previously unappreciated role for IL-15 in the differentiation of human monocytes towards killer DCs. The observation that IL-15 DCs have killer DC capacity lends further support to their implementation in DC-based immunotherapy protocols.
References
[1]
Lanier LL, Testi R, Bindl J, Phillips JH (1989) Identity of Leu-19 (CD56) leukocyte differentiation antigen and neural cell adhesion molecule. J Exp Med 169: 2233–2238.
[2]
Spits H, Lanier LL (2007) Natural killer or dendritic: what's in a name? Immunity 26: 11–16.
[3]
Hanna J, Gonen-Gross T, Fitchett J, Rowe T, Daniels M, et al. (2004) Novel APC-like properties of human NK cells directly regulate T cell activation. J Clin Invest 114: 1612–1623.
[4]
Pillarisetty VG, Katz SC, Bleier JI, Shah AB, Dematteo RP (2005) Natural killer dendritic cells have both antigen presenting and lytic function and in response to CpG produce IFN-gamma via autocrine IL-12. J Immunol 174: 2612–2618.
[5]
Chan CW, Crafton E, Fan HN, Flook J, Yoshimura K, et al. (2006) Interferon-producing killer dendritic cells provide a link between innate and adaptive immunity. Nat Med 12: 207–213.
[6]
Taieb J, Chaput N, Menard C, Apetoh L, Ullrich E, et al. (2006) A novel dendritic cell subset involved in tumor immunosurveillance. Nat Med 12: 214–219.
[7]
Blasius AL, Barchet W, Cella M, Colonna M (2007) Development and function of murine B220+CD11c+NK1.1+ cells identify them as a subset of NK cells. J Exp Med 204: 2561–2568.
[8]
Vosshenrich CA, Lesjean-Pottier S, Hasan M, Richard-Le Goff O, Corcuff E, et al. (2007) CD11cloB220+ interferon-producing killer dendritic cells are activated natural killer cells. J Exp Med 204: 2569–2578.
[9]
Caminschi I, Ahmet F, Heger K, Brady J, Nutt SL, et al. (2007) Putative IKDCs are functionally and developmentally similar to natural killer cells, but not to dendritic cells. J Exp Med 204: 2579–2590.
[10]
Wesa AK, Storkus WJ (2008) Killer dendritic cells: mechanisms of action and therapeutic implications for cancer. Cell Death Differ 15: 51–57.
[11]
Chauvin C, Josien R (2008) Dendritic cells as killers: Mechanistic aspects and potential roles. J Immunol 181: 11–16.
[12]
Larmonier N, Fraszczak J, Lakomy D, Bonnotte B, Katsanis E (2010) Killer dendritic cells and their potential for cancer immunotherapy. Cancer Immunol Immunother 59: 1–11.
[13]
Drobits B, Holcmann M, Amberg N, Swiecki M, Grundtner R, et al. (2012) Imiquimod clears tumors in mice independent of adaptive immunity by converting pDCs into tumor-killing effector cells. J Clin Invest 122: 575–585.
[14]
Chan CW, Housseau F (2008) The 'kiss of death' by dendritic cells to cancer cells. Cell Death Differ 15: 58–69.
[15]
Anguille S, Van Tendeloo V, Berneman Z (2012) Dendritic cell-based therapeutic vaccination for acute myeloid leukemia. Bull Cancer 99: 635–642.
[16]
Anguille S, Willemen Y, Lion E, Smits EL, Berneman ZN (2012) Dendritic cell vaccination in acute myeloid leukemia. Cytotherapy 14: 647–656.
[17]
Anguille S, Smits ELJM, Cools N, Goossens H, Berneman ZN, et al. (2009) Short-term cultured, interleukin-15 differentiated dendritic cells have potent immunostimulatory properties. J Transl Med 7: 109.
[18]
Jonuleit H, Kuhn U, Muller G, Steinbrink K, Paragnik L, et al. (1997) Pro-inflammatory cytokines and prostaglandins induce maturation of potent immunostimulatory dendritic cells under fetal calf serum-free conditions. Eur J Immunol 27: 3135–3142.
[19]
Anguille S, Lion E, Smits E, Berneman ZN, van Tendeloo VF (2011) Dendritic cell vaccine therapy for acute myeloid leukemia: questions and answers. Hum Vaccin 7: 579–584.
[20]
Smits EL, Anguille S, Cools N, Berneman ZN, Van Tendeloo VF (2009) Dendritic cell-based cancer gene therapy. Hum Gene Ther 20: 1106–1118.
[21]
Mohamadzadeh M, Berard F, Essert G, Chalouni C, Pulendran B, et al. (2001) Interleukin 15 skews monocyte differentiation into dendritic cells with features of Langerhans cells. J Exp Med 194: 1013–1020.
[22]
Dubsky P, Saito H, Leogier M, Dantin C, Connolly JE, et al. (2007) IL-15-induced human DC efficiently prime melanoma-specific naive CD8+ T cells to differentiate into CTL. Eur J Immunol 37: 1678–1690.
[23]
Harris KM (2011) Monocytes differentiated with GM-CSF and IL-15 initiate Th17 and Th1 responses that are contact-dependent and mediated by IL-15. J Leukoc Biol 90: 727–734.
[24]
Provasi E, Genovese P, Lombardo A, Magnani Z, Liu PQ, et al. (2012) Editing T cell specificity towards leukemia by zinc finger nucleases and lentiviral gene transfer. Nat Med 18: 807–815.
[25]
Lion E, Anguille S, Berneman ZN, Smits EL, Van Tendeloo VF (2011) Poly(I:C) enhances the susceptibility of leukemic cells to NK cell cytotoxicity and phagocytosis by DC. PLoS One 6: e20952.
[26]
Milush JM, Long BR, Snyder-Cappione JE, Cappione AJ, York VA, et al. (2009) Functionally distinct subsets of human NK cells and monocyte/DC-like cells identified by coexpression of CD56, CD7, and CD4. Blood 114: 4823–4831.
[27]
Walzer T, Jaeger S, Chaix J, Vivier E (2007) Natural killer cells: from CD3(?)NKp46(+) to post-genomics meta-analyses. Curr Opin Immunol 19: 365–372.
[28]
Lanier LL, Chang C, Phillips JH (1994) Human NKR-P1A. A disulfide-linked homodimer of the C-type lectin superfamily expressed by a subset of NK and T lymphocytes. J Immunol 153: 2417–2428.
[29]
Steinman RM, Nussenzweig MC (1980) Dendritic cells: features and functions. Immunol Rev 53: 127–147.
[30]
Anguille S, Van Tendeloo VF, Berneman ZN (2012) Leukemia-associated antigens and their relevance to the immunotherapy of acute myeloid leukemia. Leukemia 26: 2186–2196.
[31]
Welte S, Kuttruff S, Waldhauer I, Steinle A (2006) Mutual activation of natural killer cells and monocytes mediated by NKp80-AICL interaction. Nat Immunol 7: 1334–1342.
[32]
Palucka K, Banchereau J (2012) Cancer immunotherapy via dendritic cells. Nat Rev Cancer 12: 265–277.
[33]
Figdor CG, de Vries IJ, Lesterhuis WJ, Melief CJ (2004) Dendritic cell immunotherapy: mapping the way. Nat Med 10: 475–480.
[34]
Farag SS, Caligiuri MA (2006) Human natural killer cell development and biology. Blood Rev 20: 123–137.
[35]
Bigley V, Spence LE, Collin M (2010) Connecting the dots: monocyte/DC and NK subsets in human peripheral blood. Blood 116: 2859–2860.
[36]
Robertson MJ, Caligiuri MA, Manley TJ, Levine H, Ritz J (1990) Human natural killer cell adhesion molecules. Differential expression after activation and participation in cytolysis. J Immunol 145: 3194–3201.
[37]
Pittet MJ, Speiser DE, Valmori D, Cerottini JC, Romero P (2000) Cutting edge: cytolytic effector function in human circulating CD8+ T cells closely correlates with CD56 surface expression. J Immunol 164: 1148–1152.
[38]
Santin AD, Hermonat PL, Ravaggi A, Bellone S, Roman JJ, et al. (2001) Expression of CD56 by human papillomavirus E7-specific CD8+ cytotoxic T lymphocytes correlates with increased intracellular perforin expression and enhanced cytotoxicity against HLA-A2-matched cervical tumor cells. Clin Cancer Res 7: 804s–810s.
[39]
Cookson S, Reen D (2003) IL-15 drives neonatal T cells to acquire CD56 and become activated effector cells. Blood 102: 2195–2197.
[40]
Kelly-Rogers J, Madrigal-Estebas L, O'Connor T, Doherty DG (2006) Activation-induced expression of CD56 by T cells is associated with a reprogramming of cytolytic activity and cytokine secretion profile in vitro. Hum Immunol 67: 863–873.
[41]
Alexander AA, Maniar A, Cummings JS, Hebbeler AM, Schulze DH, et al. (2008) Isopentenyl pyrophosphate-activated CD56+ {gamma}{delta} T lymphocytes display potent antitumor activity toward human squamous cell carcinoma. Clin Cancer Res 14: 4232–4240.
[42]
Urban EM, Li H, Armstrong C, Focaccetti C, Cairo C, et al. (2009) Control of CD56 expression and tumor cell cytotoxicity in human Vgamma2Vdelta2 T cells. BMC Immunol 10: 50.
[43]
Correia MP, Costa AV, Uhrberg M, Cardoso EM, Arosa FA (2011) IL-15 induces CD8+ T cells to acquire functional NK receptors capable of modulating cytotoxicity and cytokine secretion. Immunobiology 216: 604–612.
[44]
Fanger NA, Maliszewski CR (1999) Schooley K, Griffith TS (1999) Human dendritic cells mediate cellular apoptosis via tumor necrosis factor-related apoptosis-inducing ligand (TRAIL). J Exp Med 190: 1155–1164.
[45]
Schmitz M, Zhao S, Deuse Y, Schakel K, Wehner R, et al. (2005) Tumoricidal potential of native blood dendritic cells: direct tumor cell killing and activation of NK cell-mediated cytotoxicity. J Immunol 174: 4127–4134.
[46]
Papewalis C, Jacobs B, Wuttke M, Ullrich E, Baehring T, et al. (2008) IFN-alpha skews monocytes into CD56(+)-expressing dendritic cells with potent functional activities in vitro and in vivo. J Immunol 180: 1462–1470.
[47]
Anguille S, Lion E, Willemen Y, Van Tendeloo VF, Berneman ZN, et al. (2011) Interferon-alpha in acute myeloid leukemia: an old drug revisited. Leukemia 25: 739–748.
[48]
Kalb ML, Glaser A, Stary G, Koszik F, Stingl G (2012) TRAIL+ human plasmacytoid dendritic cells kill tumor cells in vitro: mechanisms of imiquimod- and IFN-alpha-mediated antitumor reactivity. J Immunol 188: 1583–1591.
[49]
Lacasse CJ, Janikashvili N, Larmonier CB, Alizadeh D, Hanke N, et al. (2011) Th-1 lymphocytes induce dendritic cell tumor killing activity by an IFN-gamma-dependent mechanism. J Immunol 187: 6310–6317.
[50]
Chapoval AI, Tamada K, Chen L (2000) In vitro growth inhibition of a broad spectrum of tumor cell lines by activated human dendritic cells. Blood 95: 2346–2351.
[51]
Vidalain PO, Azocar O, Yagita H, Rabourdin-Combe C, Servet-Delprat C (2001) Cytotoxic activity of human dendritic cells is differentially regulated by double-stranded RNA and CD40 ligand. J Immunol 167: 3765–3772.
[52]
Manna PP, Mohanakumar T (2002) Human dendritic cell mediated cytotoxicity against breast carcinoma cells in vitro. J Leukoc Biol 72: 312–320.
[53]
Stary G, Bangert C, Tauber M, Strohal R, Kopp T, et al. (2007) Tumoricidal activity of TLR7/8-activated inflammatory dendritic cells. J Exp Med 204: 1441–1451.
[54]
Manna PP, Hira SK, Das AA, Bandyopadhyay S, Gupta KK (2012) IL-15 activated human peripheral blood dendritic cell kill allogeneic and xenogeneic endothelial cells via apoptosis. Cytokine 61: 118–126.
[55]
Matsui T, Connolly JE, Michnevitz M, Chaussabel D, Yu CI, et al. (2009) CD2 distinguishes two subsets of human plasmacytoid dendritic cells with distinct phenotype and functions. J Immunol 182: 6815–6823.
[56]
Koski GK, Koldovsky U, Xu S, Mick R, Sharma A, et al. (2012) A novel dendritic cell-based immunization approach for the induction of durable Th1-polarized anti-HER-2/neu responses in women with early breast cancer. J Immunother 35: 54–65.
[57]
Tel J, Smits EL, Anguille S, Joshi RN, Figdor CG, et al. (2012) Human plasmacytoid dendritic cells are equipped with antigen presenting- and tumoricidal-capacities. Blood 120: 3936–3944.
[58]
Luckey U, Maurer M, Schmidt T, Lorenz N, Seebach B, et al. (2011) T cell killing by tolerogenic dendritic cells protects mice from allergy. J Clin Invest 121: 3860–3871.
[59]
Suss G, Shortman K (1996) A subclass of dendritic cells kills CD4 T cells via Fas/Fas-ligand-induced apoptosis. J Exp Med 183: 1789–1796.
[60]
Barblu L, Machmach K, Gras C, Delfraissy JF, Boufassa F, et al. (2012) Plasmacytoid dendritic cells from HIV controllers produce IFN-alpha and differentiate into functional killer pDC under HIV activation. J Infect Dis 206: 790–801.
[61]
Choy JC, Hung VH, Hunter AL, Cheung PK, Motyka B, et al. (2004) Granzyme B induces smooth muscle cell apoptosis in the absence of perforin: involvement of extracellular matrix degradation. Arterioscler Thromb Vasc Biol 24: 2245–2250.
[62]
Pardo J, Wallich R, Ebnet K, Iden S, Zentgraf H, et al. (2007) Granzyme B is expressed in mouse mast cells in vivo and in vitro and causes delayed cell death independent of perforin. Cell Death Differ 14: 1768–1779.
[63]
Pipkin ME, Lieberman J (2007) Delivering the kiss of death: progress on understanding how perforin works. Curr Opin Immunol 19: 301–308.
[64]
Thiery J, Keefe D, Boulant S, Boucrot E, Walch M, et al. (2011) Perforin pores in the endosomal membrane trigger the release of endocytosed granzyme B into the cytosol of target cells. Nat Immunol 12: 770–777.