NIH-funded research R01 grant

Endothelial inflammation and Src kinase in early pulmonary arterial hypertension

Official title: Endothelial Inflammation, Src Kinase Dysregulation, and Fibrosis in Early Pulmonary Arterial Hypertension

Funded at Brigham and Women's Hospital · NIH-11411210 · Data updated 2026-11-12

Researchers are studying how inflammation in the lining of blood vessels and a protein called Src kinase contribute to early lung artery remodeling in people with mild PAH.

More Hypertension research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionBrigham and Women's Hospital
NIH-funded
Lab location1 site (Boston, United States)
Project startSeptember 15, 2025
Project endJune 30, 2030
Funding year2026
Award (this year)$739,659
NIH project number5R01HL176637-02
Project IDNIH-11411210 on NIH RePORTER

Who could benefit from this research

Could help

Adults with or at risk for pulmonary arterial hypertension, especially those with inflammatory connective tissue disease–associated PAH, could be relevant for future translational work or trials arising from this research.

Less likely to help

Individuals without PAH or those not connected to the study’s inflammatory CTD context may not directly benefit from this research.

What this research studies

This project aims to understand how endothelial inflammation drives fibrosis and vessel remodeling in early PAH using a model of endothelial inflammation and human PAH cell data. It focuses on the role of C-terminal Src kinase (Csk) as a mediator of endothelial dysfunction and fibrosis, and on identifying molecular pathways connected to inflammatory CTD risk. By linking network medicine analysis with experimental models, the study seeks to reveal targets that could prevent progression before severe disease develops. The findings could inform future therapies to reduce right heart strain and improve outcomes in patients with inflammatory CTD-associated PAH.

Why it matters

Potential benefit: If successful, the research could identify new targets to halt or slow vascular remodeling in early PAH, potentially improving survival and quality of life for patients.

How similar studies have gone: Prior work has shown that targeting inflammatory pathways and Src signaling can influence vascular remodeling in PAH models, supporting potential translational relevance here.

Where this research is happening

  • Brigham and Women's Hospital
    Boston, United States
    Active

Researchers

  • Principal investigator: Wertheim, Bradley — Brigham and Women's Hospital
  • Study coordinator: Wertheim, Bradley

Related research

Other NIH-funded projects on the same topics.

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.