From: Conventional type 1 dendritic cells (cDC1) in cancer immunity
Cancer type | Study | Finding | References |
---|---|---|---|
Bladder cancer | Preclinical | cDC1 and CD8+ T cells confer immune surveillance and responses to intravesical CD40 agonism | [75] |
Breast cancer | Preclinical | Anti-TIM-3 antibody improved response to paclitaxel chemotherapy was cDC1 dependent | [45] |
Breast cancer | Correlative | Gene signatures of cDC1 were associated with increased overall survival | [40] |
Breast and pancreatic cancer | Preclinical | Tumor-produced granulocyte-stimulating factor downregulated IRF8 in cDC progenitors and interrupted cDC1 development | [50] |
Breast cancer (LBC, TNBC) | Correlative | Gene signatures of cDC1 are associated with increased overall patient survival | [39] |
Breast cancer | Preclinical | cDC1 interferon signaling was required for T-cell mediated protective responses to breast cancer | [76] |
Fibrosarcoma | Preclinical | Rejection of tumors was impaired in cDC1 deficient mice | [77] |
Fibrosarcoma | Preclinical | Lack of CD103+ DC within the tumor microenvironment dominantly resists the effector phase of an anti-tumor T cell response, contributing to immune escape | [44] |
Hepatocellular carcinoma | Preclinical | CD47 blockade enhanced tumor DNA uptake by cDC1 and stimulated the cGAS-STING-dependent infiltration of NK cells in liver cancer | [78] |
Liver-engrafted tumors | Preclinical | Depletion of cDC1 in established tumors suppressed immunotherapy efficacy of anti-PD-1 and/or anti-CD137 as well as adoptive T-cell therapy | [79] |
Lung cancer | Prognostic and in vitro | cDC1s cross-present human tumor antigen after uptake of necrotic lung cancer cells | [80] |
Lung carcinoma and melanoma-induced lung metastasis | Preclinical | Lung tumor development led to the accumulation of regulatory CD103loCD11b+ DC and a reduced proportion of cDC1 | [81] |
Non-small cell lung cancer (NSCLC) | Preclinical | Paucity of cDC1s contributes to reduced antitumor immunity | [82] |
Melanoma | Preclinical | Recruitment of cDC1s into tumors was necessary for a CD8+ T cell responses | [83] |
Melanoma | Preclinical | Efficacy of immunomodulatory anti-CD137 and anti-PD-1 immunotherapy required cDC1 | [84] |
Melanoma | Preclinical | cDC1 transported antigens to lymph nodes and primed CD8+ T cells and promoted anti-tumor effects upon PD-L1 ICI. Combined FLT3L and poly I:C therapy enhanced tumor responses to checkpoint and BRAF blockade | [46] |
Melanoma | Preclinical | cDC1 enhanced activation of TCR-engineered T cells | [85] |
Melanoma | Predictive | cDC1 among total antigen-presenting cells predicted patient responsiveness to anti-PD-1 therapy | [86] |
Melanoma and osteosarcoma | Preclinical | Vaccination with poly I:C-activated and tumor antigen-loaded cDC1s enhanced tumor infiltration of tumor antigen-specific and interferon-γ+ CD8+ T cells, and suppressed tumor growth | [87] |
Melanoma | Preclinical | Administration of Fms-related tyrosine 3 ligand (Flt3L) plus polyI:C and anti-CD40 resulted in an increase of activated cDC1 treated tumors and delayed tumor growth | [88] |
Melanoma | Correlative | Human CD141+ cDC1 from blood are impaired in patients with advanced melanoma | [89] |
Melanoma | Preclinical | Inhibition of the mevalonate pathway in cancer cells triggers cDC1-mediated anticancer immunity | [90] |
Melanoma, colorectal cancer | Preclinical | Therapeutic efficacy dead cell antigen-loaded cDC1s was synergistic with anti-PD-1 therapy | [91] |
Melanoma, colorectal carcinoma; several human cancer types | Preclinical; prognostic | FLT3LG and CCL5 or CCR5 gene expression signatures correlate with an enhanced cDC1 signature and a favorable overall survival in patients with cancer | [54] |
Multiple human tumor biopsies | Correlative | Abundance of cDC1 transcripts correlated with clinical outcome | [92] |
Ovarian cancer | Preclinical | PD-1 blockade enabled tumor-associated cDC1s to promote disease clearance | [93] |
Ovarian cancer (OvC) and prostate cancer (PrC) | Correlative | cDC1s are reduced in patients with OvC, and are quantitatively and qualitatively impaired in patients with OvC or PrC | [56] |
Pancreatic ductal adenocarcinoma (PDAC) | Preclinical | PDAC antigen-loaded cDC1s used as a vaccine, rendering PDAC sensitive to ICI with curative outcome | [94] |