A New Way to Deliver Gene Editing Therapies for Blood Disorders #medicine #biotech #innovation @harvardengineering
A New Way to Deliver Gene Editing Therapies for Blood Disorders #medicine #biotech #innovation  @harvardengineering
Uploaded May 2026 | Updated September 2026, 1 week ago
What if gene editing treatments could be delivered directly inside the body—making them faster, more accessible, and less invasive? In this video, Omolivie Eboreime, a bioengineering student at the Harvard John A. Paulson School of Engineering and Applied Sciences, presents his project on developing protein nanoparticles to deliver gene-editing therapies for hemoglobinopathies.

Current treatments, including those based on CRISPR gene editing, often require removing a patient’s stem cells, editing them outside the body, and reinfusing them—an intensive and resource-heavy process. Omar’s approach aims to deliver gene-editing cargo directly into the body, reducing the need for complex procedures and making treatments more accessible—especially in low-resource settings where hemoglobin disorders are most prevalent.
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A New Way to Deliver Gene Editing Therapies for Blood Disorders #medicine #biotech #innovation

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