Experimental Drug TY1 Reverses Systemic Sclerosis Effects in Preclinical Study
核心洞察
Cedars-Sinai investigators used the experimental drug TY1 to reverse the effects of systemic sclerosis (搜索), a life-threatening autoimmune disease, in a laboratory study published in JCI Insight.
TY1 reduced inflammation and DNA damage in immune cells from patients and improved heart function, physical activity, and organ scarring in a mouse model of the disease.
The drug is a synthetic noncoding RNA developed at Cedars-Sinai that blocks the basic immune system pathway driving systemic sclerosis (搜索), making it a potential future therapy.
Investigators at Cedars-Sinai Health Sciences University (搜索) used an experimental drug to reverse the effects of systemic sclerosis (搜索), a serious autoimmune disease, in a laboratory study published in JCI Insight. The drug, called TY1, blocked the basic immune system pathway driving the disease, positioning it as a potential future therapy for a condition that currently has no cure.
Systemic sclerosis (搜索), also called scleroderma, is a chronic, life-threatening condition that scars the skin, lungs, heart and other organs. Because there is no cure or known cause for the disease, which affects about 100,000 people in the U.S., treatments focus on relieving symptoms.
"That's why we are so excited about our findings," said Eduardo Marbán, MD, PhD, executive director of the Smidt Heart Institute at Cedars-Sinai and corresponding author of the study. "The basic immune system pathway driving systemic sclerosis (搜索) is blocked by this new drug, making it a potential future therapy."
Mechanism and Preclinical Findings
TY1, which was developed at Cedars-Sinai, is a synthetic version of a type of noncoding ribonucleic acid (RNA), a molecule that regulates cellular processes. After using TY1 to reduce tissue damage in laboratory experiments addressing heart attacks, as reported last year, investigators sought to determine if TY1 might have a similar effect on autoimmune disorders.
Investigators tested TY1 on immune cells collected from patients with systemic sclerosis (搜索) and found that the drug reduced inflammation and DNA damage in those cells. When they administered TY1 to laboratory mice with a condition that mimics systemic sclerosis, investigators found that heart function and physical activity improved, and scar formation in organs was reduced.
"We chose to test TY1 in systemic sclerosis (搜索) because the science of how the drug works makes sense and also because it is such a devastating disease," said Ahmed Ibrahim, PhD, MPH, associate professor of Cardiology at Cedars-Sinai and a co-investigator of the study.
Path Toward Clinical Development
Investigators are currently preparing an investigational new drug application to the U.S. Food and Drug Administration, the first step toward obtaining approval for studying TY1 in people with systemic sclerosis (搜索).
"This innovative study illustrates how doing careful research on one disease can lead to key discoveries on another — in this case, from conditions that can stiffen the heart to scleroderma, a rare disease that hardens the skin and internal organs in patients who have waited decades for better treatment options," said Susan Cheng, MD, chair of the Department of Cardiology in the Smidt Heart Institute.
The work was supported by National Institutes of Health funding, including grants R01HL164588 and T32HL116273, and by the California Institute for Regenerative Medicine (TRAN1-15317). Eduardo Marbán owns founder's equity in Capricor (搜索), and Ahmed Ibrahim owns stock in Capricor; Capricor has no relationship with this project and no licensing rights to the discoveries reported.