Tumour-associated macrophages as a potential target to improve natural killer cell-based immunotherapies

Adoptive transfer of natural killer (NK) cells has been proposed as a novel immunotherapy for malignant tumours resistant to current therapeutic modalities. Several clinical studies have demonstrated that the NK cell-infusion is well tolerated without severe side effects and shows promising results in haematological malignancies. However, patients with malignant solid tumours do not show significant responses to this therapy. Such disappointing results largely arise from the inefficient delivery of infused NK cells and the impairment of their functions in the tumour microenvironment (TME). Tumour-associated macrophages (TAMs) are the most abundant stromal cells in the TME of most solid tumours, and a high TAM density correlates with poor prognosis of cancer patients. Although our knowledge of the interactions between TAMs and NK cells is limited, many studies have indicated that TAMs suppress NK cell cytotoxicity against cancer cells. Therefore, blockade of TAM functions can be an attractive strategy to improve NK cell-based immunotherapies. On the other hand, macrophages are reported to activate NK cells under certain circumstances. This essay presents our current knowledge about mechanisms by which macrophages regulate NK cell functions and discusses possible therapeutic approaches to block macrophage-mediated NK cell suppression.

[1]  Dechuan Li,et al.  Upregulation of HMGB1 in tumor-associated macrophages induced by tumor cell-derived lactate further promotes colorectal cancer progression , 2023, Journal of Translational Medicine.

[2]  J. N. Arnold,et al.  The effects of radiation therapy on the macrophage response in cancer , 2022, Frontiers in Oncology.

[3]  J. Pathak,et al.  Tumor-associated macrophage-specific CD155 contributes to M2-phenotype transition, immunosuppression, and tumor progression in colorectal cancer , 2022, Journal for ImmunoTherapy of Cancer.

[4]  Jing Gao,et al.  Shaping Polarization Of Tumor-Associated Macrophages In Cancer Immunotherapy , 2022, Frontiers in Immunology.

[5]  Binzhi Qian,et al.  Macrophage diversity in cancer revisited in the era of single-cell omics. , 2022, Trends in immunology.

[6]  Xianwei Yang,et al.  Comprehensive Molecular Analyses of a Macrophage-Related Gene Signature With Regard to Prognosis, Immune Features, and Biomarkers for Immunotherapy in Hepatocellular Carcinoma Based on WGCNA and the LASSO Algorithm , 2022, Frontiers in Immunology.

[7]  K. E. El Kasmi,et al.  CD206+ tumor-associated macrophages cross-present tumor antigen and drive antitumor immunity , 2022, JCI insight.

[8]  F. Ginhoux,et al.  Tissue-resident FOLR2+ macrophages associate with CD8+ T cell infiltration in human breast cancer , 2022, Cell.

[9]  G. Bernardini,et al.  NK Cell Anti-Tumor Surveillance in a Myeloid Cell-Shaped Environment , 2021, Frontiers in Immunology.

[10]  N. Jiang,et al.  The Landscape of PDK1 in Breast Cancer , 2021, Cancers.

[11]  Amit A. Patel,et al.  Cross-tissue single-cell landscape of human monocytes and macrophages in health and disease. , 2021, Immunity.

[12]  Yichi Zhang,et al.  Defects in Macrophage Reprogramming in Cancer Therapy: The Negative Impact of PD-L1/PD-1 , 2021, Frontiers in Immunology.

[13]  T. Cotechini,et al.  Tissue-Resident and Recruited Macrophages in Primary Tumor and Metastatic Microenvironments: Potential Targets in Cancer Therapy , 2021, Cells.

[14]  T. D. de Gruijl,et al.  Natural Killer Cells and Anti-Cancer Therapies: Reciprocal Effects on Immune Function and Therapeutic Response , 2021, Cancers.

[15]  Jiang Ren,et al.  Targeting TGFβ signal transduction for cancer therapy , 2021, Signal Transduction and Targeted Therapy.

[16]  T. Kitamura,et al.  Metastasis-associated macrophages constrain antitumor capability of natural killer cells in the metastatic site at least partially by membrane bound transforming growth factor β , 2021, Journal for ImmunoTherapy of Cancer.

[17]  D. Lane,et al.  Targeting a scavenger receptor on tumor-associated macrophages activates tumor cell killing by natural killer cells , 2020, Proceedings of the National Academy of Sciences.

[18]  A. Mantovani,et al.  Antagonistic Inflammatory Phenotypes Dictate Tumor Fate and Response to Immune Checkpoint Blockade , 2020, Immunity.

[19]  Jeffrey S. Miller,et al.  Exploring the NK cell platform for cancer immunotherapy , 2020, Nature Reviews Clinical Oncology.

[20]  N. Gray,et al.  Extracellular-Regulated Protein Kinase 5-Mediated Control of p21 Expression Promotes Macrophage Proliferation Associated with Tumor Growth and Metastasis , 2020, Cancer Research.

[21]  Hua Wang,et al.  NK Cell-Based Immune Checkpoint Inhibition , 2020, Frontiers in Immunology.

[22]  J. Pardo,et al.  Recalling the Biological Significance of Immune Checkpoints on NK Cells: A Chance to Overcome LAG3, PD1, and CTLA4 Inhibitory Pathways by Adoptive NK Cell Transfer? , 2020, Frontiers in Immunology.

[23]  D. Campana,et al.  NK cells for cancer immunotherapy , 2020, Nature Reviews Drug Discovery.

[24]  Juan Du,et al.  Myeloid deletion of phosphoinositide-dependent kinase-1 enhances NK cell-mediated antitumor immunity by mediating macrophage polarization , 2020, Oncoimmunology.

[25]  A. Steinle,et al.  Impairment of NKG2D-Mediated Tumor Immunity by TGF-β , 2019, Front. Immunol..

[26]  B. Dai,et al.  Tumor-associated macrophages expressing galectin-9 identify immunoevasive subtype muscle-invasive bladder cancer with poor prognosis but favorable adjuvant chemotherapeutic response , 2019, Cancer Immunology, Immunotherapy.

[27]  Lucy Ireland,et al.  Blockade of Stromal Gas6 Alters Cancer Cell Plasticity, Activates NK Cells, and Inhibits Pancreatic Cancer Metastasis , 2019, bioRxiv.

[28]  F. Locatelli,et al.  Killer Ig-Like Receptors (KIRs): Their Role in NK Cell Modulation and Developments Leading to Their Clinical Exploitation , 2019, Front. Immunol..

[29]  D. Sterner,et al.  TAM receptors attenuate murine NK‐cell responses via E3 ubiquitin ligase Cbl‐b , 2019, European journal of immunology.

[30]  J. Kzhyshkowska,et al.  Interaction of tumor-associated macrophages and cancer chemotherapy , 2019, Oncoimmunology.

[31]  J. Pollard,et al.  Targeting macrophages: therapeutic approaches in cancer , 2018, Nature Reviews Drug Discovery.

[32]  Gang Li,et al.  Natural Killer Cell-Based Cancer Immunotherapy: A Review on 10 Years Completed Clinical Trials , 2018, Cancer investigation.

[33]  Shuwen Liu,et al.  The Role of Toll-Like Receptor in Inflammation and Tumor Immunity , 2018, Front. Pharmacol..

[34]  T. Kitamura,et al.  Macrophage targeting: opening new possibilities for cancer immunotherapy , 2018, Immunology.

[35]  R. Sun,et al.  Blockade of the checkpoint receptor TIGIT prevents NK cell exhaustion and elicits potent anti-tumor immunity , 2018, Nature Immunology.

[36]  S. Asthana,et al.  A natural killer–dendritic cell axis defines checkpoint therapy–responsive tumor microenvironments , 2018, Nature Medicine.

[37]  B. Becher,et al.  CSF1R-dependent myeloid cells are required for NK‑mediated control of metastasis. , 2018, JCI insight.

[38]  M. Gandhi,et al.  Immune evasion via PD-1/PD-L1 on NK cells and monocyte/macrophages is more prominent in Hodgkin lymphoma than DLBCL. , 2018, Blood.

[39]  R. Coffman,et al.  Combination immunotherapy with TLR agonists and checkpoint inhibitors suppresses head and neck cancer. , 2017, JCI insight.

[40]  G. Lal,et al.  The Molecular Mechanism of Natural Killer Cells Function and Its Importance in Cancer Immunotherapy , 2017, Front. Immunol..

[41]  R. Jesenofsky,et al.  Interleukin-15 stimulates natural killer cell-mediated killing of both human pancreatic cancer and stellate cells , 2017, Oncotarget.

[42]  N. Beauchemin,et al.  CEACAM1 as a multi-purpose target for cancer immunotherapy , 2017, Oncoimmunology.

[43]  E. Tagliabue,et al.  Activation of NK cell cytotoxicity by aerosolized CpG-ODN/poly(I:C) against lung melanoma metastases is mediated by alveolar macrophages. , 2017, Cellular immunology.

[44]  J. Wargo,et al.  Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy , 2017, Cell.

[45]  Y. Zhuang,et al.  Tumor-Associated Monocytes/Macrophages Impair NK-Cell Function via TGFβ1 in Human Gastric Cancer , 2017, Cancer Immunology Research.

[46]  M. Kolb,et al.  M2‐polarized and tumor‐associated macrophages alter NK cell phenotype and function in a contact‐dependent manner , 2017, Journal of leukocyte biology.

[47]  M. Rantalainen,et al.  Reprogramming Tumor-Associated Macrophages by Antibody Targeting Inhibits Cancer Progression and Metastasis. , 2016, Cell reports.

[48]  A. Ribas,et al.  Combination cancer immunotherapies tailored to the tumour microenvironment , 2016, Nature Reviews Clinical Oncology.

[49]  X. Liu,et al.  Increased Tim-3 expression in peripheral NK cells predicts a poorer prognosis and Tim-3 blockade improves NK cell-mediated cytotoxicity in human lung adenocarcinoma. , 2015, International immunopharmacology.

[50]  M. Locati,et al.  Priming of Human Resting NK Cells by Autologous M1 Macrophages via the Engagement of IL-1β, IFN-β, and IL-15 Pathways , 2015, The Journal of Immunology.

[51]  Yuan Yuan,et al.  The Clinical Significance of Abnormal Tim-3 Expression on NK Cells from Patients with Gastric Cancer , 2015, Immunological investigations.

[52]  R. Childs,et al.  Genetic Manipulation of NK Cells for Cancer Immunotherapy: Techniques and Clinical Implications , 2015, Front. Immunol..

[53]  Benjamin G. Gowen,et al.  A shed NKG2D ligand that promotes natural killer cell activation and tumor rejection , 2015, Science.

[54]  J. Pollard,et al.  Immune cell promotion of metastasis , 2015, Nature Reviews Immunology.

[55]  J. Wargo,et al.  Effective Innate and Adaptive Antimelanoma Immunity through Localized TLR7/8 Activation , 2014, The Journal of Immunology.

[56]  L. Moretta,et al.  Effect of tumor cells and tumor microenvironment on NK‐cell function , 2014, European journal of immunology.

[57]  A. Mantovani,et al.  TLR activation of tumor‐associated macrophages from ovarian cancer patients triggers cytolytic activity of NK cells , 2014, European journal of immunology.

[58]  Xuan Cheng,et al.  T-cell Immunoglobulin and ITIM Domain (TIGIT) Receptor/Poliovirus Receptor (PVR) Ligand Engagement Suppresses Interferon-γ Production of Natural Killer Cells via β-Arrestin 2-mediated Negative Signaling* , 2014, The Journal of Biological Chemistry.

[59]  A. Ullrich,et al.  The E3 ligase Cbl-b and TAM receptors regulate cancer metastasis via natural killer cells , 2014, Nature.

[60]  V. Kuchroo,et al.  Reversal of NK-Cell Exhaustion in Advanced Melanoma by Tim-3 Blockade , 2014, Cancer Immunology Research.

[61]  W. Pan,et al.  Monocyte/macrophage‐elicited natural killer cell dysfunction in hepatocellular carcinoma is mediated by CD48/2B4 interactions , 2013, Hepatology.

[62]  F. Hentges,et al.  Mouse Lung and Spleen Natural Killer Cells Have Phenotypic and Functional Differences, in Part Influenced by Macrophages , 2012, PloS one.

[63]  C. Li,et al.  Recruitment of Grb2 and SHIP1 by the ITT-like motif of TIGIT suppresses granule polarization and cytotoxicity of NK cells , 2012, Cell Death and Differentiation.

[64]  Z. Tian,et al.  Macrophages Help NK Cells to Attack Tumor Cells by Stimulatory NKG2D Ligand but Protect Themselves from NK Killing by Inhibitory Ligand Qa-1 , 2012, PloS one.

[65]  A. Jha,et al.  Tim-3 marks human natural killer cell maturation and suppresses cell-mediated cytotoxicity. , 2012, Blood.

[66]  T. Niki,et al.  Tim-3 is an inducible human natural killer cell receptor that enhances interferon gamma production in response to galectin-9. , 2012, Blood.

[67]  A. Luttun,et al.  Malignant cells fuel tumor growth by educating infiltrating leukocytes to produce the mitogen Gas6. , 2010, Blood.

[68]  N. Stanietsky,et al.  The interaction of TIGIT with PVR and PVRL2 inhibits human NK cell cytotoxicity , 2009, Proceedings of the National Academy of Sciences.

[69]  E. Clementi,et al.  Inflammatory and alternatively activated human macrophages attract vessel‐associated stem cells, relying on separate HMGB1‐ and MMP‐9‐dependent pathways , 2009, Journal of leukocyte biology.

[70]  H. Rammensee,et al.  Interaction of Monocytes with NK Cells upon Toll-Like Receptor-Induced Expression of the NKG2D Ligand MICA1 , 2008, The Journal of Immunology.

[71]  Eric Vivier,et al.  Functions of natural killer cells , 2008, Nature Immunology.

[72]  É. Vivier,et al.  Sustained NKG2D engagement induces cross-tolerance of multiple distinct NK cell activation pathways. , 2008, Blood.

[73]  J. Trowsdale,et al.  Reciprocal regulation of human natural killer cells and macrophages associated with distinct immune synapses. , 2007, Blood.

[74]  M. Sandusky,et al.  Regulation of 2B4 (CD244)‐mediated NK cell activation by ligand‐induced receptor modulation , 2006, European journal of immunology.

[75]  Qingxian Lu,et al.  Natural killer cell differentiation driven by Tyro3 receptor tyrosine kinases , 2006, Nature Immunology.

[76]  A. Hayday,et al.  Sustained localized expression of ligand for the activating NKG2D receptor impairs natural cytotoxicity in vivo and reduces tumor immunosurveillance , 2005, Nature Immunology.

[77]  P. Loke,et al.  PD-L1 and PD-L2 are differentially regulated by Th1 and Th2 cells , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[78]  D. Pardoll,et al.  Expression of Programmed Death 1 Ligands by Murine T Cells and APC1 , 2002, The Journal of Immunology.

[79]  B. Huard,et al.  LAG-3 does not define a specific mode of natural killing in human. , 1998, Immunology letters.

[80]  B. Wollenberg,et al.  Absence of B7.1‐CD28/CTLA‐4‐mediated co‐stimulation in human NK cells , 1998, European journal of immunology.