How the HAVCR2 (TIM3) gene affects brain immune cells in late-onset Alzheimer's

Role of a novel risk loci HAVCR2 of late-onset Alzheimer's disease in the regulation of microglial response in neurodegeneration

NIH-funded research Brigham and Women's Hospital · NIH-11298969

This project is looking at whether differences in the HAVCR2 (TIM3) gene change how brain immune cells (microglia) behave in people with late-onset Alzheimer's disease.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionBrigham and Women's Hospital NIH-funded
Lab location1 site (Boston, United States)
Project IDNIH-11298969 on NIH RePORTER

What this research studies

From a patient perspective, researchers are studying a gene called HAVCR2 (also known as TIM3) that is active in brain immune cells called microglia and linked to late-onset Alzheimer's. They will use human gene data and lab experiments including genetically altered mice and cell-based tests to see how turning TIM3 on or off changes microglial activity, plaque clearance, and inflammatory signaling. The team will study the TGF-beta–TIM3 pathway and use genetic deletion and molecular assays to measure phagocytosis and plaque effects in an Alzheimer's mouse model. Findings will be compared to human microglial gene patterns to guide whether TIM3 could be a target for future therapies.

Who could benefit from this research

Good fit: Ideal candidates would be people with late-onset Alzheimer's disease or brain/tissue donors whose samples can be used to study microglial TIM3 biology.

Not a fit: People with other types of dementia, early-onset familial Alzheimer's driven by different genes, or those not able to provide samples are unlikely to directly benefit from this preclinical work.

Why it matters

Potential benefit: If successful, this work could point to new ways to boost microglia to clear amyloid plaques or lead to TIM3-targeted treatments for late-onset Alzheimer's.

How similar studies have performed: TIM3-targeting approaches have shown promise in cancer immunotherapy and TIM3 deletion reduced plaque burden in Alzheimer's mouse models, but targeting TIM3 in human Alzheimer's remains largely untested.

Where this research is happening

Boston, 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 Alzheimer disease dementiaAlzheimer disease treatmentAlzheimer syndromeAlzheimer's Disease
Last reviewed 2026-06-13 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.