Target intelligence / Profile preview

Defensin beta 110 (DEFB110)

Target
DEFB110
Molecular classification
Antimicrobial peptide, Innate immune effector, Cationic peptide, Beta-defensin family
01

Overview

Defensin beta 110 (DEFB110) is a member of the beta-defensin family, a group of small, cationic antimicrobial peptides produced in neutrophils and epithelial tissues. Beta-defensins, including DEFB110, possess broad-spectrum antimicrobial activity and form part of the innate immune response by disrupting microbial membranes through a pore-forming mechanism governed by their conserved cysteine-rich structure. In addition to direct microbicidal action, beta-defensins contribute to immune cell recruitment and modulation of immune responses, enhancing both innate and adaptive immunity. The expression of DEFB110, like other beta-defensins, is tightly clustered genomically, and their roles may extend from frontline defense (preventing infection in mucosal and epithelial surfaces) to more complex immune system functions. No drugs are currently known to target DEFB110 directly, and no disease-modifying roles or biomarker utilities unique to this isoform are established in the literature.

Other names
Defensin beta 110DEFB110DEFB10DEFB11DEFB111Beta-defensin 110Beta-defensin 10Beta-defensin 11Beta-defensin 111Defensin, beta 110Defensin, beta 111defensin, beta 110 locusbeta-defensin 110beta-defensin 10beta-defensin 11beta-defensin 111
02

Mechanism of action

Not applicable; DEFB110 acts as an endogenous antimicrobial peptide—not typically a direct therapeutic target for existing drugs

03

Biological functions

Antimicrobial activity (broad-spectrum, against Gram-positive and Gram-negative bacteria, fungi, and enveloped viruses)Innate immune defenseChemotaxis of immune cells (such as monocytes, T lymphocytes, dendritic cells, and mast cells)Enhancement of macrophage phagocytosisModulation of cytokine and chemokine responses (in some beta-defensins)
04

Disease associations

Infection (primary protective role against infectious organisms)Potentially inflammation and immune regulation (by affecting immune cell chemotaxis and cytokine induction)No direct established link to cancer, neurodegenerative, or cardiovascular disease
05

Safety considerations

No safety or therapeutic challenge data specific to DEFB110; potential for immune system overactivation is a general concern for modulating defensins
06

Interacting drugs

None known; no drugs currently reported to selectively target or modulate DEFB110
07

Biomarkers

None established for DEFB110 specifically; in general, some defensins are being explored as biomarkers for infection or immune status but DEFB110-specific data are lacking

Beyond the preview

Go deeper on Defensin beta 110 (DEFB110).

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 Defensin beta 110 (DEFB110).

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