NIH-funded research R01 grant

How immune cells drive lung blood-vessel disease in schistosomiasis

Official title: Activation, Phenotype and Function of CD4 T Cells in Schistosoma-Pulmonary Hypertension

Funded at University of California, San Francisco · NIH-11417075 · Data updated 2026-11-12

This work looks at how specific immune cells in people with schistosomiasis may cause high blood pressure in the lungs and who might be at risk.

More Hypertension research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of California, San Francisco
NIH-funded
Lab location1 site (San Francisco, United States)
Project startDecember 15, 2016
Project endAugust 31, 2027
Funding year2025
Award (this year)$45,681
NIH project number3R01HL135872-09S2
Project IDNIH-11417075 on NIH RePORTER

Who could benefit from this research

Could help

Ideal participants would be people with severe schistosomiasis, particularly those with signs or a diagnosis of pulmonary arterial hypertension or at high risk for lung vascular disease.

Less likely to help

People without schistosomiasis or those whose pulmonary hypertension has a clearly different cause may not directly benefit from this research.

What this research studies

Researchers use a mouse model that mimics schistosomiasis-linked lung blood-vessel disease to follow the immune steps that lead to vessel scarring. They focus on CD4 Th2 immune cells, how those T cells pull in CCR2+ monocytes that produce thrombospondin-1 (TSP-1), and how TSP-1 activates TGF-β to remodel vessels. The team will compare those animal findings with proteins and samples from people with severe schistosomiasis to find matching signals. Combining the animal experiments and human biospecimens is meant to map the immune chain of events that produces pulmonary hypertension.

Why it matters

Potential benefit: If successful, this work could reveal biological markers and new targets for treatments to prevent or slow lung high blood pressure in people with schistosomiasis.

How similar studies have gone: Prior mouse studies from this group have already outlined a Th2–monocyte–TSP-1–TGF-β pathway driving schistosoma-linked pulmonary hypertension, but applying those findings to human samples is more recent and less proven.

Where this research is happening

  • University of California, San Francisco
    San Francisco, United States
    Active

Researchers

  • Principal investigator: Graham, Brian Barkley — University of California, San Francisco
  • Study coordinator: Graham, Brian Barkley

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.