Personalized Immunomonitoring for Juvenile Dermatomyositis
Official title: Personalized Immunomonitoring to Understand Juvenile Dermatomyositis
Funded at Weill Medical Coll of Cornell Univ · NIH-11384572 · Data updated 2026-11-12
A personalized approach to monitoring immune signals in kids with juvenile dermatomyositis to better understand and track their disease.
Quick facts
| Grant type | R01 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | Weill Medical Coll of Cornell Univ NIH-funded |
| Lab location | 1 site (New York, United States) |
| Project start | August 1, 2025 |
| Project end | June 30, 2030 |
| Funding year | 2026 |
| Award (this year) | $674,047 |
| NIH project number | 5R01AR084711-02 |
| Project ID | NIH-11384572 on NIH RePORTER |
Who could benefit from this research
✓Could help
Ideal candidates are children and adolescents diagnosed with juvenile dermatomyositis who consent to longitudinal immune monitoring.
✕Less likely to help
Patients without JDM or those unable to participate in regular sample collection may not benefit directly.
What this research studies
This project focuses on children with juvenile dermatomyositis (JDM), a systemic autoimmune condition that affects the skin, muscles, and sometimes lungs or heart. By studying autoantibodies, immune cell subsets, and interferon activity, researchers aim to map how the disease behaves in individual patients. The team will collect and analyze samples over time to find minimally invasive ways to diagnose and measure disease activity and course. The goal is to move beyond broad immunosuppression to more precise, patient-specific care.
Why it matters
Potential benefit: If successful, this work could lead to better and earlier ways to monitor disease activity and personalize treatment for children with JDM.
How similar studies have gone: Previous research shows that autoimmune diseases, including pediatric myositis, exhibit heterogeneity and potential biomarkers, but robust, noninvasive monitoring tools are still emerging.
Where this research is happening
-
Weill Medical Coll of Cornell Univ
New York, United States Active
Researchers
- Principal investigator: Pascual, Maria Virginia — Weill Medical Coll of Cornell Univ
- Study coordinator: Pascual, Maria Virginia
Related research
Other NIH-funded projects on the same topics.
-
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.
-
Precision therapies for dermatomyositis using single-cell RNA data and bioinformatics
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.
-
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.
-
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.
-
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.
-
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.