Turning “Cold” Tumors “Hot”: Immune Activation Mechanisms and Intervention Strategies
Turning “Cold” Tumors “Hot”: Immune Activation Mechanisms and Intervention Strategies
“Cold” tumors are generally characterized by insufficient tumor antigen presentation, limited effector T-cell infiltration, and pronounced local immunosuppression, resulting in relatively poor responses to immune checkpoint blockade. “Hot” tumors exhibit more active inflammatory responses, abundant tumor-infiltrating lymphocytes, and a more complete cancer-immunity cycle. Enhancing tumor antigen release, activating innate immune sensing, promoting T-cell recruitment and tissue infiltration, and relieving immunosuppression can shift the tumor microenvironment from an immune-low state toward immune activation.
Keywords: cold tumors; hot tumors; tumor immunity; cGAS–STING; immunogenic cell death; T-cell infiltration; immune checkpoints; tumor microenvironment
1 Overview of “Cold” and “Hot” Tumors
1.1 Immune Characteristics of “Hot” Tumors
“Hot” tumors generally contain relatively high levels of infiltrating CD8⁺ T cells and show enhanced inflammatory and chemotactic signals, including type I interferons, IFN-γ, CXCL9, and CXCL10. Tumor antigens can be captured, processed, and presented by dendritic cells, while primed tumor-specific T cells enter tumor tissues and recognize target cells. Persistent immune selection pressure may also induce negative-feedback mechanisms such as PD-L1 upregulation, making these tumors more likely to benefit from immune checkpoint blockade targeting PD-1/PD-L1 and related pathways.
1.2 “Cold” Tumors Do Not Represent a Single Immune State
(1) Immune-Desert Tumors
Immune-desert tumors lack effective T-cell priming and show little infiltration of effector lymphocytes within either the tumor parenchyma or surrounding tissues. This state may involve insufficient tumor antigens, abnormal antigen processing and presentation, impaired dendritic cell function, and inadequate innate immune sensing.
(2) Immune-Excluded Tumors
Immune-excluded tumors are not completely devoid of T cells. Instead, T cells are mainly distributed within the tumor stroma or invasive margin and fail to enter cancer cell-rich regions. Abnormal tumor vasculature, a dense extracellular matrix, enhanced TGF-β signaling, and myeloid immunosuppression can create spatial and functional barriers that restrict T-cell entry into the tumor parenchyma.
1.3 “Hot” Tumors May Still Exhibit Immune Dysfunction
Some tumors contain substantial T-cell infiltration but also show persistent antigen stimulation, enhanced inhibitory signaling through PD-1/PD-L1, LAG-3, and TIM-3, and immunosuppressive mechanisms involving regulatory T cells, myeloid-derived suppressor cells, and adenosine metabolism. Tumor-infiltrating T cells may consequently become exhausted or functionally restricted. The “cold–hot” classification primarily reflects the overall inflammatory and infiltrative characteristics of the tumor immune microenvironment and cannot independently serve as an absolute predictor of immunotherapy efficacy.
Comparison Dimension | “Cold” Tumors | “Hot” Tumors |
CD8⁺ T-cell infiltration | Low or mainly restricted to the tumor margin | Relatively abundant, with infiltration into the tumor parenchyma |
Tumor antigen presentation | Frequently limited by insufficient antigen availability or abnormal MHC-I presentation | Relatively active |
Innate immune signaling | Relatively weak cGAS–STING and type I interferon signaling | More active inflammatory and interferon-associated signaling |
Chemokines | Insufficient CXCL9, CXCL10, and related chemokine expression | Relatively high CXCL9 and CXCL10 expression |
Microenvironmental characteristics | Immune desert, immune exclusion, or pronounced myeloid suppression | Prominent inflammatory infiltration, although T-cell exhaustion may still occur |
PD-1/PD-L1 pathway | May be low or overshadowed by other immunosuppressive mechanisms | Frequently accompanied by adaptive PD-L1 upregulation |
Sensitivity to immune checkpoint blockade | Generally relatively low | Relatively high, but responses are not universal |
2 Mechanisms Underlying Immune-Low Tumor States
2.1 Insufficient Tumor Antigen Generation and Presentation
Effective antitumor immunity initially depends on tumor antigens that can be recognized by the immune system. Low tumor mutational burden, reduced antigen expression, and immunoediting can decrease tumor immunogenicity. Abnormalities in β2-microglobulin, the MHC-I antigen-presentation system, and associated antigen-processing mechanisms can further impair the display of tumor antigens on the cell surface and reduce the efficiency with which cytotoxic T cells recognize tumor cells.
2.2 Insufficient Innate Immune Sensing
Tumor-derived DNA entering the cytosol can be recognized by cGAS, which catalyzes the production of 2′,3′-cGAMP and subsequently activates STING–TBK1–IRF3 signaling and type I interferon production. Type I interferons contribute to dendritic cell maturation, antigen cross-presentation, and T-cell priming. Some tumors maintain low-inflammatory and immune-low states by reducing cGAS–STING pathway activity, enhancing cGAMP degradation, or suppressing interferon signaling.
2.3 Restricted T-Cell Recruitment and Tumor Infiltration
Activated T cells migrate toward tumor tissues in response to chemotactic signals such as CXCL9, CXCL10, and CXCL11. Some immune-low tumors lack effective chemokine expression and exhibit VEGF-driven abnormal vasculature in which endothelial adhesion molecule expression and vascular permeability are unfavorable for lymphocyte transendothelial migration. Cancer-associated fibroblasts and a dense extracellular matrix can create additional spatial barriers that restrict T-cell entry into the tumor parenchyma.
2.4 The Immunosuppressive Tumor Microenvironment
Regulatory T cells, PMN-MDSCs, and immunosuppressive tumor-associated macrophages can inhibit effector T cells through TGF-β, IL-10, ARG1, ROS, and related pathways. CD39–CD73-mediated conversion of extracellular ATP into adenosine, VEGF-driven abnormal vasculature, hypoxia, and lactate accumulation can further reduce T-cell activity, preventing effector lymphocytes that have already entered tumor tissues from maintaining sustained antitumor functions.
Formation Stage | Representative Mechanisms | Major Immune Consequences |
Insufficient tumor antigens | Low mutational burden, reduced antigen expression, immunoediting | Inadequate priming of tumor-specific T cells |
Impaired antigen presentation | Abnormal MHC-I, β2-microglobulin, or antigen processing | Reduced immune recognition of tumor cells |
Insufficient innate immune sensing | Reduced cGAS–STING, TLR, or type I interferon signaling | Impaired dendritic cell maturation and cross-presentation |
Insufficient T-cell recruitment | Reduced CXCL9/CXCL10 expression | Decreased migration of effector T cells toward tumors |
Vascular barrier | VEGF-driven abnormal vasculature | Restricted lymphocyte transendothelial migration |
Stromal exclusion | TGF-β, CAFs, and extracellular matrix remodeling | Retention of T cells at tumor margins or within the stroma |
Myeloid immunosuppression | MDSCs, TAMs, ARG1, and ROS | Reduced T-cell proliferation and effector function |
Metabolic suppression | Adenosine, lactate, and hypoxia | Restricted T-cell activation and cytotoxicity |
3 Key Mechanisms for Converting the Tumor Immune Microenvironment from “Cold” to “Hot”
3.1 Enhancing Tumor Antigen Release
Radiotherapy, certain chemotherapies, oncolytic viruses, and other interventions capable of inducing immunogenic cell death (ICD) can promote tumor antigen release. These treatments may also induce damage-associated molecular pattern changes, including ATP release, HMGB1 release, and calreticulin exposure. Such alterations increase the immunogenicity of dying tumor cells and provide a basis for dendritic cell-mediated tumor antigen uptake and subsequent T-cell priming.
3.2 Activating Innate Immunity and Dendritic Cells
Cytosolic DNA–cGAS–STING signaling and pattern-recognition receptors such as TLRs convert tumor-derived nucleic acid signals into type I interferon and inflammatory responses. After receiving maturation signals, dendritic cells capture, process, and cross-present tumor antigens and prime tumor-specific CD8⁺ T cells in tumor-draining lymph nodes, helping establish adaptive antitumor immunity within immune-desert microenvironments.
3.3 Promoting Effector T-Cell Recruitment and Tissue Infiltration
Type I interferon- and IFN-γ-associated signaling can promote the expression of chemokines such as CXCL9 and CXCL10 and enhance the migration of CXCR3⁺ effector T cells toward tumor tissues. Improving abnormal tumor vasculature, reducing VEGF signaling, and weakening TGF-β-associated stromal barriers may further promote T-cell transendothelial migration and entry into the tumor parenchyma, shifting immune-excluded tumors toward an immune-infiltrated state.
3.4 Restoring the Effector Function of Tumor-Infiltrating T Cells
Increased T-cell infiltration does not necessarily produce effective antitumor immunity. Persistent antigen stimulation can induce inhibitory receptors such as PD-1, TIM-3, and LAG-3, while tumor cells and myeloid cells can further restrict T-cell function through PD-L1, adenosine, and a metabolically suppressive environment. Blocking immune checkpoints and other immunosuppressive pathways can restore the proliferation, cytokine secretion, and cytotoxic activity of tumor-infiltrating T cells.
4 Major Strategies for Converting Tumors from “Cold” to “Hot”
4.1 Inducing Immunogenic Cell Death
Radiotherapy can cause DNA double-strand breaks, micronucleus formation, and cytosolic DNA accumulation, activating cGAS–STING signaling under appropriate conditions. Certain chemotherapeutic agents, including anthracyclines and Oxaliplatin, can also induce tumor cell death with immunogenic characteristics. Tumor antigen release and exposure of damage-associated signals can jointly promote dendritic cell recruitment and antigen presentation, establishing a more favorable immune basis for subsequent immune checkpoint blockade.
4.2 Activating the cGAS–STING and TLR Pathways
(1) The cGAS–STING Pathway
2′,3′-cGAMP, diABZI, and other STING agonists enhance STING–TBK1–IRF3 signaling and promote type I interferon production, helping restore innate immune sensing in tumors and local immune cells. STING activation can also promote dendritic cell maturation, CD8⁺ T-cell priming, and inflammatory chemokine expression.
(2) TLR Pathways
Pattern-recognition receptors such as TLR3, TLR7/8, and TLR9 recognize different nucleic acid signals. TLR agonists can activate dendritic cells and other innate immune cells and increase type I interferon and inflammatory cytokine production, thereby strengthening immune-priming signals in tumors with low baseline inflammation.
4.3 Remodeling Local Tumor Immunity with Oncolytic Viruses
Oncolytic viruses can selectively replicate in tumor cells or induce tumor cell lysis while releasing tumor antigens, viral nucleic acids, and inflammatory signals. Local viral infection can enhance dendritic cell activation and T-cell recruitment and alter cytokine and immune checkpoint expression within tumors, providing an immunological basis for combination with immune checkpoint blockade.
4.4 Targeting Tumor Vascular and Stromal Barriers
VEGF not only promotes tumor angiogenesis but also contributes to structurally abnormal, unevenly perfused vasculature with insufficient immune cell adhesion. Appropriate inhibition of VEGF/VEGFR signaling can promote vascular normalization and improve immune cell infiltration. Extracellular matrix remodeling mediated by TGF-β and cancer-associated fibroblasts can produce spatial T-cell exclusion, and targeting these structural barriers may increase the density of effector T cells within the tumor parenchyma.
4.5 Relieving Myeloid Immunosuppression
CXCL–CXCR2 signaling promotes the recruitment of neutrophils and PMN-MDSCs, whereas pathways such as CSF1–CSF1R contribute to the recruitment and maintenance of tumor-associated macrophages. Blocking the recruitment of protumor myeloid cells or reprogramming their functional states can reduce immunosuppressive factors such as ARG1, ROS, and IL-10 and help restore CD8⁺ T-cell infiltration and effector activity.
4.6 Combination with Immune Checkpoint Blockade
PD-1/PD-L1 blockade primarily acts on pre-existing antitumor T cells whose functions have been suppressed. Immune checkpoint inhibitors alone therefore generally have limited activity in immune-desert tumors. Combining PD-1/PD-L1 blockade with STING or TLR agonists, oncolytic viruses, radiotherapy, vascular normalization, or myeloid cell-targeted interventions can address distinct barriers involving insufficient antigen release, impaired T-cell priming, restricted infiltration, and suppression of local effector function.
Intervention Strategy | Primary Stage | Representative Mechanism | Effect on the Immune Microenvironment |
Immunogenic cell death | Antigen release | ICD, DAMPs, and cytosolic DNA formation | Increases antigen availability and danger signals |
cGAS–STING activation | Innate immune priming | STING–TBK1–IRF3 and type I interferons | Promotes dendritic cell maturation and T-cell priming |
TLR activation | Innate immune priming | TLR3, TLR7/8, and TLR9 | Enhances inflammatory cytokine and interferon responses |
Oncolytic viruses | Antigen release and local inflammation | Tumor lysis and viral nucleic acid sensing | Increases local tumor immunogenicity |
VEGF/VEGFR intervention | Vascular barrier | Vascular normalization | Improves immune cell infiltration into tissues |
TGF-β/stromal intervention | Spatial exclusion | CAF and extracellular matrix remodeling | Promotes T-cell entry into the tumor parenchyma |
CXCR2/myeloid intervention | Myeloid immunosuppression | Reduced recruitment of PMN-MDSCs and related cells | Reduces myeloid-derived immunosuppression |
PD-1/PD-L1 blockade | T-cell effector stage | Release of immune checkpoint inhibition | Restores the effector function of tumor-infiltrating T cells |
5 Research Progress in Converting Tumors from “Cold” to “Hot”
5.1 T-VEC
(1) Oncolytic Virus-Mediated Immune Activation
Talimogene laherparepvec (T-VEC) is an engineered HSV-1 oncolytic virus that induces local tumor cell lysis and expresses GM-CSF. Tumor cell lysis releases antigens, while virus-derived nucleic acids and inflammatory signals further promote local innate immunity and antigen presentation, increasing immune activation within the tumor microenvironment.
(2) Immunotherapy for Melanoma
T-VEC has been used as a local treatment for unresectable melanoma and has further supported studies combining oncolytic viruses with PD-1/PD-L1 blockade. These studies demonstrate that, in addition to directly destroying tumor cells, local oncolytic therapy can contribute to systemic antitumor immunity by altering the tumor immune microenvironment and lymphocyte infiltration.
5.2 Vidutolimod
(1) TLR9 Activation
Vidutolimod (CMP-001) is a virus-like particle-based TLR9 agonist strategy that activates plasmacytoid dendritic cells and enhances type I interferon responses, promoting antigen presentation and effector T-cell recruitment.
(2) Studies in PD-1-Resistant Tumors
Vidutolimod combined with PD-1 blockade has been studied in melanoma that progressed after previous PD-1 treatment. Some patients showed increased intratumoral T-cell infiltration and antitumor responses, supporting evaluation of whether innate immune activation can restore sensitivity to immune checkpoint blockade.
5.3 BO-112
(1) Double-Stranded RNA-Mediated Innate Immune Activation
BO-112 consists of nanoplexed double-stranded RNA. Following intratumoral administration, it activates RNA-sensing innate immune pathways and induces type I interferon production, immunogenic cell death, and local inflammatory responses, allowing tumor antigen release and innate immune activation to occur simultaneously.
(2) Combination Studies with Immune Checkpoint Blockade
BO-112 has been combined with PD-1 blockade in studies involving solid tumors resistant to previous immune checkpoint therapy. These studies primarily evaluate whether local innate immune activation can increase tumor T-cell infiltration and restore sensitivity to immune checkpoint treatment.
5.4 STING Agonists
(1) Activation of STING–Type I Interferon Signaling
MIW815, MK-1454, and subsequent non-cyclic dinucleotide STING agonists have been investigated for their ability to directly activate STING, enhance type I interferon production, and promote dendritic cell function. Early intratumoral STING agonists induced local immune pharmacodynamic changes, although their antitumor activity as monotherapies remained limited.
(2) New STING Agonist Strategies
Traditional cyclic dinucleotide STING agonists are limited by intratumoral administration requirements, stability, and pharmacokinetic properties. Subsequent research has shifted toward STING agonists with improved systemic exposure, tumor-delivery capacity, or alternative molecular structures and has further explored combinations with PD-1/PD-L1 blockade and other immunotherapies.
Research Strategy | Representative Agent | Primary Targeted Stage | Research Positioning |
Oncolytic virus | T-VEC | Antigen release, local inflammation, and dendritic cell activation | Enhances tumor immunogenicity |
TLR9 activation | Vidutolimod | Plasmacytoid dendritic cells and type I interferons | Promotes immune priming and T-cell recruitment |
Double-stranded RNA activation | BO-112 | RNA sensing, ICD, and type I interferons | Remodels the local inflammatory environment |
STING activation | MIW815, MK-1454, and related agents | STING–TBK1–IRF3 | Enhances innate immunity and antigen presentation |
Immune checkpoint combination | PD-1/PD-L1 blockade | T-cell effector stage | Restores the function of infiltrating T cells |
6 Products
6.1 Products for cGAS–STING Innate Immunity Research
Catalog # | Product Name/Description | Grade & Purity | Mechanism and Research Positioning |
CGAS Human Pre-designed siRNA Set A | — | Downregulates human cGAS; used to validate the contribution of cytosolic DNA sensing and cGAS–STING signaling to tumor immune activation | |
Cgas Mouse Pre-designed siRNA Set A | — | Downregulates mouse Cgas; used to investigate innate immune sensing mechanisms in tumor models | |
Cgas Rat Pre-designed siRNA Set A | — | Downregulates rat Cgas; used in research on cGAS-dependent DNA sensing | |
cGAS-IN-1 | Moligand™, 10 mM in DMSO | Inhibits cGAS; used to validate cytosolic DNA sensing and downstream STING signaling | |
cGAS-IN-2 | ≥99% | Inhibits cGAS; used in pharmacological mechanism research involving the cGAS–STING pathway | |
cGAS-IN-4 | — | Inhibits cGAS; used to evaluate cGAS-dependent type I interferon responses | |
STING1 Human Pre-designed siRNA Set A | — | Downregulates human STING1; used to validate STING-mediated tumor immune activation | |
Sting1 Mouse Pre-designed siRNA Set A | — | Downregulates mouse Sting1; used in tumor immunity models and STING functional research | |
Sting1 Rat Pre-designed siRNA Set A | — | Downregulates rat Sting1; used to investigate STING signaling mechanisms | |
Recombinant STING Antibody | Recombinant, ExactAb™, Validated, 0.4 mg/mL | Detects STING protein; used to verify pathway expression and intervention status | |
C-176 (STING inhibitor) | 10mM in DMSO | Inhibits mouse STING; used to validate STING-dependent type I interferon and inflammatory responses in murine experimental systems | |
H 151 | Moligand™, ≥98% (HPLC) | Antagonizes STING; used for pharmacological inhibition and functional validation of the STING pathway | |
cGAMP sodium salt | ≥99% | Activates STING; used to investigate STING–TBK1–IRF3 and type I interferon signaling | |
diABZI STING agonist-1 | ≥99% | Activates STING; used in dendritic cell activation and antitumor innate immunity research | |
MSA 2 | Moligand™, ≥98% (HPLC) | Activates STING; used to investigate STING-dependent immune activation within the tumor microenvironment |
6.2 Products for CXCR1/2 and Myeloid Immunosuppression Research
Catalog # | Product Name/Description | Grade & Purity | Mechanism and Research Positioning |
SB 225002 | Moligand™, ≥98% | Antagonizes CXCR2; used to investigate neutrophil and PMN-MDSC recruitment | |
SB225002 | Moligand™, 10mM in DMSO | Used in cellular studies of CXCR2-dependent chemotaxis and myeloid cell migration | |
AZD5069 | Moligand™, ≥98% | Antagonizes CXCR2; used to investigate myeloid cell recruitment and immunosuppression | |
AZD5069 | Moligand™, 10mM in DMSO | Used in cellular studies of CXCR2-mediated chemotaxis and myeloid immune regulation | |
Reparixin | Moligand™, 10mM in DMSO | Interferes with CXCR1/2-associated chemotaxis; used to investigate neutrophil and myeloid cell recruitment | |
Reparixin L-lysine salt | ≥98% (HPLC) | Used in research on the CXCL8–CXCR1/2 axis and neutrophil chemotaxis | |
danirixin | Moligand™, ≥97% | Used to investigate CXCR2-associated chemotaxis and tumor myeloid immunosuppression | |
Recombinant Human IL-8 Protein | Carrier Free, Bioactive, ActiBioPure™, His Tag, ≥95% (SDS-PAGE) | Activates CXCR1/2-associated chemotaxis; used to model IL-8-mediated myeloid cell recruitment | |
Recombinant Human CXCL5 Protein | Animal Free, Carrier Free, Bioactive, ActiBioPure™, Azide Free, High Performance, PBS Only, ≥97% (SDS-PAGE & HPLC) | Activates CXCR2-associated chemotaxis; used in neutrophil and PMN-MDSC recruitment research |
6.3 Products for Immune Checkpoint and Type I Interferon Response Research
Catalog # | Product Name/Description | Grade & Purity | Detection Target/Mechanism and Research Positioning |
PD-1/PD-L1 inhibitor 1 | ≥98% | Interferes with the PD-1/PD-L1 immune checkpoint; used to evaluate T-cell effector function following immune activation | |
PD1/CD279 Rat mAb | Carrier Free, Azide Free, Validated, PBS Only, ≥95% (SDS-PAGE), See COA | Used in PD-1-associated research and evaluation of T-cell immune checkpoint status | |
ISG15 Human Pre-designed siRNA Set A | — | Downregulates ISG15; used to investigate downstream effects of type I interferon signaling | |
Recombinant ISG15 Antibody | Recombinant, ExactAb™, Validated, High Performance, See COA | Detects ISG15 protein; used to evaluate type I interferon pathway activation | |
Recombinant ISG15 Antibody | KD Validation | Detects ISG15 protein; used in interferon-response and gene-knockdown validation studies | |
Human Ubiquitin-like Modifier (ISG15) ELISA Kit | BioReagent | Quantifies human ISG15; used to evaluate type I interferon pathway output | |
Mouse Ubiquitin-like Protein ISG15 (ISG15) ELISA Kit | BioReagent | Quantifies mouse ISG15; used to evaluate interferon responses in animal tumor models |
6.4 Products for Tumor Cell Proliferation, Death, and DNA Damage Research
Catalog # | Product Name/Description | Grade & Purity | Detection Parameter and Research Positioning |
Propidium iodide (PI) | ≥98% (HPLC) | Used to evaluate plasma membrane integrity, dead cells, and cell-cycle distribution | |
Caspase 3/7 Activity Assay Kit | BioReagent | Detects Caspase-3/7 activity; used to evaluate executioner-caspase activation during apoptosis | |
LDH Cytotoxicity Assay Kit with WST-8 | BioReagent, Ready-to-use, for IP | Detects LDH release; used to evaluate tumor cell injury and cytotoxicity | |
Z-VAD-FMK | Moligand™, 10mM in DMSO | Broad-spectrum Caspase inhibitor used to determine whether cell death is Caspase-dependent | |
RPA32/RPA2 Mouse mAb | Carrier Free, ExactAb™, Validated, High Performance, 0.5 mg/mL | Detects RPA32/RPA2; used in replication stress and DNA damage-response research | |
Recombinant RPA32/RPA2 Antibody | Recombinant, ExactAb™, Validated, See COA | Detects RPA32/RPA2; used to evaluate replication stress and DNA damage status | |
53BP1 Antibody | ExactAb™, Validated, 0.5 mg/mL | Detects 53BP1 and DNA damage foci; used in DNA double-strand break-response research |
The conversion of the tumor immune microenvironment from “cold” to “hot” fundamentally involves re-establishing the cancer-immunity cycle comprising tumor antigen release, innate immune sensing, T-cell priming and recruitment, infiltration into tumor tissues, and effector-mediated killing. Because the limiting stages differ substantially among tumors, mechanism-based stratification of interventions targeting antigen insufficiency, immune deserts, spatial exclusion, and local immunosuppression represents an important direction for improving immunotherapy sensitivity.
References
[1] Chen DS, Mellman I. Elements of cancer immunity and the cancer-immune set point. Nature. 2017;541:321–330.
[2] Galon J, Bruni D. Approaches to treat immune hot, altered and cold tumours with combination immunotherapies. Nat Rev Drug Discov. 2019;18:197–218.
[3] Hegde PS, Chen DS. Top 10 challenges in cancer immunotherapy. Immunity. 2020;52(1):17–35.
[4] Demaria O, Cornen S, Daëron M, Morel Y, Medzhitov R, Vivier E. Harnessing innate immunity in cancer therapy. Nature. 2019;574:45–56.
[5] Ribas A, Wolchok JD. Cancer immunotherapy using checkpoint blockade. Science. 2018;359:1350–1355.
[6] Corrales L, McWhirter SM, Dubensky TW Jr, Gajewski TF. The host STING pathway at the interface of cancer and immunity. J Clin Invest. 2016;126(7):2404–2411.
[7] Galluzzi L, Humeau J, Buqué A, Zitvogel L, Kroemer G. Immunostimulation with chemotherapy in the era of immune checkpoint inhibitors. Nat Rev Clin Oncol. 2020;17:725–741.
For more related articles, please see below:
[1] HMGB1-Mediated Damage-Associated Inflammatory Signaling and Tumor Immune Regulation
[2] How NKG2A and NKG2D Jointly Regulate Tumor Immune Killing
[4] How Does Dynamic ECM Remodeling in the Tumor Microenvironment Regulate Tumor Immune Responses?
[5] mtDNA Stress and cGAS–STING/AIM2 Innate Immune Activation Mediated by CRAT Deficiency
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