NIH-funded research R01 grant

S100A9+ immune cells driving liver scarring in MASLD/MASH

Official title: S100A9+ macrophages and monocytic myeloid-derived suppressor cells as drivers of liver fibrosis in MASLD/MASH

Funded at Massachusetts General Hospital · NIH-11429726 · Data updated 2026-11-12

Affects people with MASLD/MASH may benefit from a better understanding of how certain immune cells contribute to liver fibrosis and how to stop it.

More Fibrosis research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionMassachusetts General Hospital
NIH-funded
Lab location1 site (Boston, United States)
Project startSeptember 1, 2026
Project endMay 31, 2030
Funding year2026
Award (this year)$850,096
NIH project number1R01DK148711-01
Project IDNIH-11429726 on NIH RePORTER

Who could benefit from this research

Could help

Adults with MASLD/MASH who have or are at risk of liver fibrosis.

Less likely to help

Patients without MASLD/MASH or without liver inflammation/fibrosis may not benefit directly.

What this research studies

This project looks at how immune cells called M-MDSCs and S100A9+ macrophages may push liver scarring in MASLD/MASH. Using patient samples and advanced analysis, researchers will map how these cells interact with liver cells to promote fibrosis. The work aims to pinpoint targets to interrupt this harmful signaling and prevent progression to worse disease. The study will combine single-cell analyses with functional tests to test key ideas in human tissues and models that reflect patient biology.

Why it matters

Potential benefit: If successful, the findings could lead to new strategies to reduce liver fibrosis in MASLD/MASH patients.

How similar studies have gone: Preliminary human data suggest immune cells contribute to fibrosis, but the specific S100A9+ macrophage pathway in MASLD/MASH is still being explored.

Where this research is happening

  • Massachusetts General Hospital
    Boston, United States
    Active

Researchers

  • Principal investigator: Alatrakchi, Nadia — Massachusetts General Hospital
  • Study coordinator: Alatrakchi, Nadia

Related research

Other NIH-funded projects on the same topics.

  • Role of SMAD1/5/8 signaling in liver fibrosis

    This grant explores how specific liver cell signals influence scarring (fibrosis) in the liver, with a focus on people who have alcohol-related liver disease or related conditions.

    NIH research University of Arizona · Tucson, United States · NIH-11504353

  • Targeting TGF-βRII to treat alcoholic liver fibrosis

    A study to test a new peptide that blocks a key fibrosis signal and a gene-silencing approach to help reverse liver fibrosis caused by alcohol use.

    NIH research University of Missouri Kansas City · Kansas City, United States · NIH-11466092

  • Understanding how RNA binding proteins drive liver scarring and how to slow it down

    A researcher team is studying how certain RNA binding proteins, especially LARP6, regulate the liver’s scar-building process in alcoholic liver disease to identify potential ways to reduce fibrosis.

    NIH research Sanford Burnham Prebys Medical Discovery Institute · La Jolla, United States · NIH-11449893

  • Liver fibrosis test platform using patient-derived liver tissue to speed anti-fibrosis drugs

    A patient-focused liver fibrosis test platform is being developed to help speed the creation of medicines that treat liver scarring by using human-derived liver cells and tissue signals.

    NIH research Xylyx Bio, INC. · Brooklyn, United States · NIH-11413845

  • Role of HK2 in liver scarring, fatty liver disease, and liver cancer

    A study in adults looks at how the enzyme HK2 helps drive liver scarring in NASH and may influence the development of liver cancer, with potential to point to new treatments.

    NIH research University of Illinois at Chicago · Chicago, UNITED STATES · NIH-11400510

  • Novel Paxillin-FAK Inhibitors for Liver Fibrosis

    A new program is testing Paxillin-FAK inhibitors to slow or stop liver fibrosis in adults with liver diseases like alcoholic liver disease and MASH.

    NIH research Faknostics, LLC · Phoenix, United States · NIH-11387961

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.
Last reviewed 2026-11-14 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.