Target intelligence / Profile preview

Tumor and immune cells

Molecular classification
Other
01

Overview

The interaction between tumor and immune cells occurs within the tumor microenvironment (TME), a complex cellular ecosystem that dictates cancer progression and therapeutic response (Binnewies et al., 2018, Nature Medicine). Tumor cells often exploit inhibitory pathways, such as the PD-1/PD-L1 axis, to suppress the activity of cytotoxic T lymphocytes and evade immunosurveillance (Pardoll, 2012, Nature Reviews Cancer). Modern immunotherapy aims to disrupt these interactions using monoclonal antibodies or to enhance immune recognition through engineered cells like CAR-T therapies (June et al., 2018, Science). This cellular interface is characterized by a balance of pro-tumorigenic factors and anti-tumor immune responses, making it a focal point for drug development (Gajewski et al., 2013, Nature Immunology). While 'Tumor and immune cells' describes a biological system rather than a single molecular entity, it represents the primary context for the action of checkpoint inhibitors and other immunomodulatory agents (National Cancer Institute, 2023). Understanding the spatial and functional dynamics between these cell populations is essential for developing effective immunotherapies and identifying relevant biomarkers (Chen & Mellman, 2013, Immunity).

Other names
Tumor microenvironmentTMECancer-immune interfaceTumor-infiltrating immune cellsTumor-immune interactome
02

Mechanism of action

Modulation of the tumor microenvironment through immune checkpoint inhibition, cytokine signaling, or adoptive cellular transfer to restore anti-tumor immunity.

03

Biological functions

Immune responseCell proliferationApoptosisSignal transductionCell deathImmune evasion
04

Disease associations

CancerInflammation
05

Safety considerations

Immune-related adverse events (irAEs)Cytokine release syndrome (CRS)AutoimmunityTumor hyperprogressionOn-target off-tumor toxicity
06

Interacting drugs

5 more in the full profile.

07

Biomarkers

PD-L1 expressionTumor-infiltrating lymphocytes (TILs)Tumor mutational burden (TMB)Microsatellite instability (MSI)Gene expression profiling (GEP)

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