Checkpoint Ligand

CD155

The TIGIT ligand overexpressed in many cancers–an emerging checkpoint target for next-generation immunotherapy.

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Definition
CD155 (poliovirus receptor/PVR) is a cell surface adhesion molecule overexpressed in many cancers. It binds three receptors: inhibitory TIGITLoading..., inhibitory CD96, and activating CD226 (DNAM-1). In the tumor microenvironment, CD155-TIGIT interaction suppresses T cell and NK cell function. Anti-TIGIT antibodies aim to block this interaction, with multiple candidates in clinical trials.
Overexpressed
In many tumor types
Dual Role
Binds TIGIT (inhibitory) and CD226 (activating)
Immune Suppression
TIGIT engagement inhibits T/NK cells
Drug Target
Anti-TIGIT antibodies in trials

CD155 Biology

CD155 was originally identified as the poliovirus receptor but has broader functions in cell adhesion and immunity. In cancer, CD155 is overexpressed on tumor cells and myeloid cells, creating an immunosuppressive environment through TIGITLoading... engagement.

The CD155-TIGIT axis represents a druggable checkpoint distinct from PD-1/PD-L1Loading.... Anti-TIGIT antibodies (tiragolumab, vibostolimab, others) are in advanced clinical development, often combined with anti-PD-1.

Simplified

A Ligand with Two Faces: CD155 on tumor cells can connect with two different receptors on immune cells:

TIGIT: Suppresses immunity (like a brake)

CD226: Activates immunity (like an accelerator)

Same ligand, opposite effects depending on which receptor it binds.

Measuring CD155-TIGIT Engagement

As with PD-1/PD-L1Loading..., CD155 expression doesn't guarantee TIGIT engagement. Tumors may express CD155 without functional interaction occurring–or may have high engagement despite modest expression. iFRETLoading... measurement of CD155-TIGIT interaction could identify patients whose tumors actively use this checkpoint.

The FEBS Letters review specifically notes TIGIT as an emerging checkpoint where iFRET could assess functional engagement states.

Simplified

The Problem: Measuring CD155 expression doesn't tell you which receptor is winning the competition.

The Opportunity: FRET-based measurement could potentially distinguish CD155/TIGIT engagement from CD155/CD226 engagement, revealing the functional balance in each patient's tumor.

QF-Pro Application

Exploratory

Theoretical Application: CD155 serves as ligand for both inhibitory (TIGIT) and activating (CD226) receptors. Expression alone cannot reveal which receptor pathway predominates.

QF-Pro's ability to measure specific protein-protein interactions could potentially distinguish CD155/TIGIT engagement from CD155/CD226 engagement.

Status: Theoretical application pending assay development.

Note: This represents a theoretical application based on validated QF-Pro principles. Clinical validation studies are pending. See QF-Pro ApplicationsLoading... for validated targets.
Simplified

Future potential: CD155 binds both activating and inhibitory receptors. Expression can't tell you which pathway is winning–QF-Pro could measure both interactions to find out.

CD155 Expression
IHC measures ligand presence
TIGIT Engagement
iFRET measures functional checkpoint activity

Clinical Relevance

  • Anti-TIGIT trials: CD155-TIGIT is the target of next-generation checkpoint inhibitorsLoading...
  • Combination rationale: Often combined with anti-PD-1 based on preclinical synergy
  • Patient selection: Functional engagement measurement could identify likely responders
  • Resistance mechanisms: TIGITLoading... pathway may mediate resistance to anti-PD-1

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