How the body senses cell injury through a new danger-signal receptor

Immunobiology of a novel human DAMP receptor, its murine homolog, & their ligand

NIH-funded research Univ of Massachusetts Med Sch Worcester · NIH-11291344

This project looks at whether a newly found immune receptor in people senses a common protein released by injured cells and sets off inflammation that can damage tissues like the brain and heart.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniv of Massachusetts Med Sch Worcester NIH-funded
Lab location1 site (Worcester, United States)
Project IDNIH-11291344 on NIH RePORTER

What this research studies

Researchers will examine a human immune receptor called Clec17a, its mouse counterparts CD209f/g, and a widely present protein called GAPDH that may act as the alarm signal when cells are injured. They will use biochemical binding tests and structural biology to see how the receptor and GAPDH interact. Experiments in mice will test whether blocking the receptor reduces sterile inflammation and tissue damage after injury. The team will also analyze human immune cells and clinical samples to determine whether the same pathway operates in people with injuries such as stroke or heart attack.

Who could benefit from this research

Good fit: People who have experienced recent tissue injury (for example stroke or myocardial infarction) or who can donate blood or tissue samples for research would be most relevant to this work.

Not a fit: Individuals without conditions involving acute tissue injury or those seeking immediate clinical treatments are unlikely to receive direct benefit from this basic science project.

Why it matters

Potential benefit: If successful, this work could reveal a new target to reduce harmful inflammation after tissue injury and help limit damage from stroke, heart attack, or other injury-related conditions.

How similar studies have performed: Other DAMP receptors have been linked to sterile inflammation and modulating them helped in preclinical models, but Clec17a and its interaction with GAPDH is a newly described pathway not yet tested in patients.

Where this research is happening

Worcester, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Conditions CancersCellular injury
Last reviewed 2026-06-10 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.