Target intelligence / Profile preview

Cluster of Differentiation 24–Sialic acid-binding Ig-like lectin 10 axis (CD24–Siglec-10)

Target
CD24–Siglec-10
Molecular classification
Glycosylphosphatidylinositol-linked cell-surface protein (CD24), Sialic acid-binding immunoglobulin-like lectin/receptor (Siglec-10), Immune checkpoint receptor complex
01

Overview

The CD24–Siglec-10 axis is a molecular pathway where CD24, a glycosylphosphatidylinositol-linked surface protein, interacts with Siglec-10, a sialic acid-binding immunoglobulin-like lectin predominantly expressed on macrophages and other immune cells. This interaction transmits a potent inhibitory signal that prevents phagocytosis (‘don’t eat me’ signal), mediates immunosuppression, and promotes tumor immune escape, as well as controls inflammation in infection and autoimmunity. Blockade of the axis (e.g., with anti-CD24 or anti-Siglec-10 antibodies) leads to reactivation of immune cells against tumor cells and is under investigation for immunotherapeutic approaches. CD24–Siglec-10 is implicated as an innate immune checkpoint and a promising target in cancer, infection, and autoimmune disorders, though its broad tissue expression raises safety considerations for drug targeting.

Other names
CD24/Siglec-10 axisCD24–Siglec10CD24/Siglec10 pathway
02

Mechanism of action

Blockade of CD24–Siglec-10 interaction releases macrophage phagocytosis against tumors (immune checkpoint inhibition); Activation of Siglec-10 pathway reduces inflammation and immune activation through SHP-1/SHP-2 recruitment and ITIM-mediated signaling

03

Biological functions

Immune response regulation (immunosuppression, checkpoint inhibition)Inhibition of phagocytosis ("don't eat me" signal)Control of inflammation (inhibition of TLR-mediated, NF-κB pathways)Modulation of T cell, B cell, NK cell activation
04

Disease associations

Cancer (tumor immune evasion)Infection (inflammatory response control)Autoimmune diseasesGraft-versus-host disease (GVHD)SepsisLiver injury
05

Safety considerations

CD24 is expressed in normal tissues: potential for on-target toxicity or immune suppressionAdverse immune effects due to broad expression on various immune cells
06

Interacting drugs

anti-CD24 monoclonal antibodies (ONC-781, others)

4 more in the full profile.

07

Biomarkers

CD24 expression on tumor cells for patient selection in cancer immunotherapySiglec-10 expression on macrophages/immune cellsNeoCD24 (differentiates tumor CD24 from normal tissues)

Beyond the preview

Go deeper on Cluster of Differentiation 24–Sialic acid-binding Ig-like lectin 10 axis (CD24–Siglec-10).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Cluster of Differentiation 24–Sialic acid-binding Ig-like lectin 10 axis (CD24–Siglec-10).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call