NIH-funded research Career grant

Precision therapies for dermatomyositis using single-cell RNA data and bioinformatics

Official title: Harnessing single cell RNA sequencing and integrative bioinformatics to identify precision therapeutics for dermatomyositis

Funded at University of California, San Francisco · NIH-11322715 · Data updated 2026-11-12

A doctor-scientist team at a major hospital plans to find existing drugs that could treat dermatomyositis by analyzing patient cells at the single-cell level and testing promising options in the lab.

Quick facts

Grant typeCareer grant
Study typeNIH-funded research
Funding institutionUniversity of California, San Francisco
NIH-funded
Lab location1 site (San Francisco, United States)
Project startJune 2, 2023
Project endApril 30, 2028
Funding year2026
Award (this year)$174,744
NIH project number5K08AR081983-04
Project IDNIH-11322715 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are individuals diagnosed with dermatomyositis, including both children and adults, who can provide blood and skin samples for research.

Less likely to help

Patients without dermatomyositis or those unable to provide samples would not directly benefit from this study.

What this research studies

Dermatomyositis is a rare, immune-driven condition that can affect both children and adults and often leaves people with lasting symptoms. This project uses cutting-edge single-cell RNA sequencing and network analysis to map the disease in patient immune cells and skin, then combines this information with computer-based drug repositioning to identify existing medicines that might help. Promising compounds will be tested in patient-derived blood cells and skin samples to see if they calm the disease signals in the lab. If successful, this approach could speed up finding effective, safer treatments for DM without starting from scratch. The effort is led by UC San Francisco researchers and aims to move from molecular insights toward real-world options for patients.

Why it matters

Potential benefit: If successful, the project could reveal ready-to-use drugs that target DM-specific pathways, potentially speeding access to better therapies.

How similar studies have gone: Previous DM-related research supports the feasibility of using molecular analyses to identify therapeutic targets, though this exact drug-repurposing approach is innovative for DM.

Where this research is happening

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

Researchers

  • Principal investigator: Neely, Jessica — University of California, San Francisco
  • Study coordinator: Neely, Jessica

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.