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 type | Career grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | University of California, San Francisco NIH-funded |
| Lab location | 1 site (San Francisco, United States) |
| Project start | June 2, 2023 |
| Project end | April 30, 2028 |
| Funding year | 2026 |
| Award (this year) | $174,744 |
| NIH project number | 5K08AR081983-04 |
| Project ID | NIH-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.
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Understanding why Dermatomyositis causes worse outcomes in women
A patient-centered project to understand why women with dermatomyositis, especially Black women, have more severe disease and death, and to build a regional patient registry to guide better care.
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Personalized Immunomonitoring for Juvenile Dermatomyositis
A personalized approach to monitoring immune signals in kids with juvenile dermatomyositis to better understand and track their disease.
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Identifying targeted treatments for dermatomyositis using advanced genetic analysis
This study is looking at dermatomyositis, a tough autoimmune condition, to find better and safer treatments by examining blood and skin samples from patients to see how their immune system is affected, and then using that information to repurpose existing medications.
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Understanding how skin and blood cell signals affect treatment response in children with dermatomyositis
This study is looking at why some kids with juvenile dermatomyositis don’t get better with usual treatments by checking their skin and blood for clues, so we can find better ways to help them feel better.
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Using a cannabinoid to relieve itching and inflammation in dermatomyositis
This study is looking at a new treatment that could help reduce the severe itching and inflammation caused by dermatomyositis, an autoimmune disease, and it's designed for people who are dealing with this condition.
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Anti-CD19/BCMA universal CAR-T cell therapy for refractory autoimmune diseases
This will try anti-CD19/BCMA universal CAR-T cell therapy in adults with refractory rheumatoid arthritis, dermatomyositis, systemic lupus, or systemic sclerosis to see if it is safe and can control their disease.
About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page.