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Scientists Create Miracle Human Blood Stem Cell
2 May
Summary
- Three Australian scientists created human blood stem cells after 25 years.
- The breakthrough could replace bone-marrow transplants for some patients.
- This science mimics early embryonic development in a lab.

Scientists at the Murdoch Children's Research Institute (MCRI) have successfully created human blood stem cells, a breakthrough achieved after more than 25 years of dedicated research. This complex process involves replicating early embryonic development in a laboratory, a feat described as a holy grail in stem cell science. The pioneering work by Professors Elizabeth Ng, Andrew Elefanty, and Ed Stanley is now moving towards clinical applications.
This advancement could revolutionize treatments for critically ill cancer patients, offering an alternative to bone-marrow transplants, especially for those lacking a perfectly matched donor. It also presents the possibility of correcting genetic defects in blood stem cell development. The MCRI, celebrating its 40th anniversary, has been at the forefront of numerous stem cell breakthroughs, including the creation of kidney organoids and miniature heart tissues.
Professor Elefanty highlighted the difficulty in creating these rare and complex blood stem cells, noting that overcoming these hurdles required discovering new techniques and understanding natural developmental pathways. The team meticulously controlled differentiation processes from pluripotent stem cells, mimicking early human life stages to generate the desired blood stem cells.
The critical breakthrough involved manipulating specific gene families and growth factors to direct cell development towards blood-forming endothelium. After years of refining the process, proof of concept was established when the created stem cells successfully engrafted in mice, leading to the elation of seeing human blood cells in the animals in 2020.
Human trials are now underway, paving the way for future therapies to treat bone-marrow failure and other blood disorders, including leukemia. The potential applications extend to correcting genetic defects, opening a new frontier in regenerative medicine and personalized therapies for patients with blood-related conditions.