Target intelligence / Profile preview

Programmed cell death protein 1 receptor (PD-1) (PD-1)

Target
PD-1
Molecular classification
Receptor, Immunoglobulin superfamily, Immune checkpoint, Type I transmembrane protein
01

Overview

Programmed cell death protein 1 (PD-1) is a type I transmembrane protein and a member of the immunoglobulin superfamily that functions as a critical inhibitory immune checkpoint receptor (UniProt Q15116). Primarily expressed on the surface of activated T cells, B cells, and macrophages, PD-1 plays a vital role in maintaining peripheral tolerance and preventing autoimmunity by dampening T-cell activity during inflammatory responses (NCBI Gene 5133). In many cancers, the PD-1 pathway is co-opted by tumor cells that express ligands PD-L1 and PD-L2, leading to T-cell exhaustion and immune evasion (StatPearls: NBK459363). Pembrolizumab is a high-affinity, humanized monoclonal antibody that binds to PD-1, preventing its interaction with these ligands and thereby restoring the ability of cytotoxic T cells to recognize and eliminate malignant cells (DrugBank DB09037). This therapeutic approach has demonstrated significant efficacy across a broad range of solid and hematologic malignancies, although it is frequently associated with immune-related adverse events due to the systemic loss of immune inhibition (StatPearls: NBK459363).

Other names
PDCD1CD279SLEB2hPD-1hPD-l
02

Mechanism of action

PD-1 inhibition; monoclonal antibody binding to the PD-1 receptor to block interaction with ligands PD-L1 and PD-L2, thereby reversing T-cell exhaustion and enhancing anti-tumor immune responses (StatPearls: NBK459363).

03

Biological functions

Immune responseT-cell regulationImmune toleranceApoptosisSignal transduction
04

Disease associations

CancerAutoimmune diseaseInfection
05

Safety considerations

Immune-related adverse events (irAEs)PneumonitisColitisHepatitisEndocrinopathiesNephritisDermatologic toxicity
06

Interacting drugs

16 more in the full profile.

07

Biomarkers

PD-L1 expression (TPS/CPS)Microsatellite instability-high (MSI-H)Mismatch repair deficiency (dMMR)Tumor mutational burden-high (TMB-H)

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