Therapy with patients' own p63+ progenitor cells shows promise in fatal lung disease idiopathic pulmonary fibrosis
Half a billion – that’s roughly how many tiny air sacs called alveoli make up your lungs. Alveoli are where the action happens: oxygen in, carbon dioxide out. But in the fatal disease idiopathic pulmonary fibrosis (IPF), they’re irreversibly damaged. There's currently no treatment for IPF, but now, researchers present the first clinical trial of a stem cell therapy. They isolated stem cells called P63+ airway basal progenitors from 12 IPF patients and expanded their numbers. These patients were treated with increasing doses of these cells. Those receiving higher doses showed improvements in gas transfer in their lungs and their ability to exercise. Computed tomography (CT) scans (pictured) also showed some improvement in lesions (red) in their lungs 24 weeks after treatment (right) compared to before treatment (left). This provides hope that a stem cell treatment for IPF could someday become a reality.
Written by
BPoD stands for Biomedical Picture of the Day. Managed by the MRC Laboratory of Medical Sciences until Jul 2023, it is now run independently by a dedicated team of scientists and writers. The website aims to engage everyone, young and old, in the wonders of biology, and its influence on medicine. The ever-growing archive of more than 4000 research images documents over a decade of progress. Explore the collection and see what you discover. Images are kindly provided for inclusion on this website through the generosity of scientists across the globe.
BPoD is also available in Catalan at www.bpod.cat with translations by the University of Valencia.