Active Heart, Stroke & Blood Digestion, Kidneys & Other Organs

Developmental Clinical Studies - Gene Therapy For Vein Graft Failure

In plain English

AI plain-English summary

Around half of heart bypass grafts using leg veins fail within a decade because the veins become blocked—a problem no existing drug can prevent. This trial tests whether gene therapy can stop that blockage. The researchers will take a patient’s own genes and deliver them directly into the vein wall during bypass surgery. Earlier lab work showed that this genetic intervention can keep the graft open by preventing the abnormal cell growth that narrows the vessel. The current study moves that finding into patients, assessing both safety and whether the treatment actually works. If successful, gene therapy could become a routine addition to bypass surgery, saving tens of thousands of patients each year from repeat operations, chest pain, or heart attacks. It would also open a new route for treating other types of graft failure—for example in dialysis access or peripheral artery disease—where blocked vessels are a persistent problem. The research is a direct clinical translation of fundamental discoveries in vascular biology and gene delivery, not a curiosity-driven exploration. Its impact, if positive, would be felt in operating theatres and cardiac wards within a few years.

View original technical description
Failure rates for heart bypass grafts using veins remain very high and represent a major clinical problem that lacks a drug-based treatment. Our prior studies have demonstrated the unique ability of gene therapy (the use of a patient s genes to treat the disease) to prevent the vein getting blocked which is associated with graft failure. We wish to perform a clinical trial in patients undergoing bypass grafting and assess the safety and beneficial effect of gene therapy.

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Researchers

Andrew Baker (Principal Investigator)Colin Berry (Co-Investigator)Geoff Berg (Co-Investigator)John Norrie (Co-Investigator)Keith Oldroyd (Co-Investigator)Niko Tzemos (Co-Investigator)Stuart Nicklin (Co-Investigator)

Related Research

Grants with similar aims, by meaning.

Adjunct gene therapy for coronary artery bypass surgery
Activation of long non-coding RNA by a gene therapy CRISPR/Cas9 approach to prevent vein graft failure
Gene therapy for vein graft failure (joint funding with MRC)
Arterial bioengineering of decellularised human saphenous veins to reduce early graft thrombosis and improve long-term patency rate
Potential of acellular biological scaffold coated with chemokines and cytokines as tissue engineered small artery grafts

Original classification

Research Grant

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