Researchers say the genetically engineered stem cells also could pave the way for new regenerative medicine treatments for diseases such as Type 1 diabetes.
Deepta Bhattacharya, who is on the University of Arizona Health Sciences Center for Advanced Molecular and Immunological Therapies advisory council, is a professor of immunobiology in the UArizona College of Medicine – Tucson.
One of the biggest barriers to regenerative medicine is immunological rejection by the recipient, a problem researchers at the University of Arizona Health Sciences are one step closer to solving after genetically modifying pluripotent stem cells to evade immune recognition.
The study “Engineering Human Pluripotent Stem Cell Lines to Evade Xenogeneic Transplantation Barriers” was published in the journal Stem Cell Reports last week.
Pluripotent stem cells can turn into any type of cell in the body. The findings offer a viable path forward for pluripotent stem cell-based therapies to restore tissues that are lost in diseases such as Type 1 diabetes or macular degeneration.
“There has been a lot of excitement for decades around the field of pluripotent stem cells and regenerative medicine,” said principal investigator Deepta Bhattacharya, a professor in the UArizona College of Medicine – Tucson’s Department of Immunobiology. “What we have learned from the experiences of organ transplantation is that you have to have matched donors, but the person receiving the transplant often still requires lifelong immune suppression, and that means there is increased susceptibility to infections and cancer. We’ve been trying to figure out what it is that you need to do to those stem cells to keep them from getting rejected, and it looks like we have a possible solution.”
To test their hypothesis, Bhattacharya and the research team used CRISPR-Cas9 technology, “genetic scissors” that allow scientists to make precise mutations within the genome at extremely specific locations.
Using human pluripotent stem cells, the team located the specific genes they believed were involved in immune rejection and removed them. Prior research into pluripotent stem cells and immune rejection looked at different parts of the immune system in isolation. Bhattacharya and his colleagues from The New York Stem Cell Foundation Research Institute, St. Jude Children’s Research Hospital and the Washington University School of Medicine opted to test their genetically modified stem cells in a complete and functional immune system.
“The immune system is really complicated and there are all sorts of ways it can recognize and reject things,” said Bhattacharya, a member of the UArizona Cancer Center and the BIO5 Institute who also serves on the UArizona Health Sciences Center for Molecular and Immunological Therapies advisory council.
“Transplantation across species, across the xenogeneic barrier, is difficult and is a very high bar for transplantation. We decided if we could overcome that barrier, then we could start to have confidence that we can overcome what should be a simpler human-to-human barrier, and so that’s basically what we did.”
The research team tested the modified stem cells by placing them into mice with normal, fully functioning immune systems. The results were promising – the genetically engineered pluripotent stem cells were integrated and persisted without being rejected.
“That has been the holy grail for a while,” Bhattacharya said. “You might actually have a chance of being able to perform pluripotent stem cell-based transplants without immune suppressing the person who is receiving them. That would be an important advance, both clinically and from the simple standpoint of scale. You wouldn’t have to make individualized therapies for every single person – you can start with one pluripotent stem cell type, turn it into the cell type you want and then give it to almost anyone.”
The next steps, Bhattacharya said, include testing the genetically modified pluripotent stem cells in specific disease models. He is already working with collaborators at The New York Stem Cell Foundation and the Juvenile Diabetes Research Foundation to test the technology in animal models for Type 1 diabetes.
“We needed to overcome the immune system first,” Bhattacharya said. “The next steps are how do we use these cells? We set the bar pretty high for our study and the fact that we were successful gives us some confidence that this can really work.”
Bhattacharya also is the co-founder of startup Clade Therapeutics in Boston, which licensed the technology through Tech Launch Arizona, the University of Arizona’s commercialization arm. Clade Therapeutics is establishing a robust cellular platform using stem cell-derived immune cells for the treatment of cancer and autoimmune diseases. The company said it hopes to begin clinical trials by the end of the year.
Co-authors on the paper include Hannah Pizzato, research specialist in the College of Medicine – Tucson’s Department of Immunobiology; Dr. Paula Alonso-Guallart, James Woods and Frederick J. Monsma Jr. of The New York Stem Cell Foundation Research Institute; Jon P. Connelly and Shondra M. Pruett-Miller of the St. Jude Children’s Research Hospital; and Dr. Todd A. Fehniger and John P. Atkinson of the Washington University School of Medicine.
This work was supported in part by the National Institutes of Health under award no. R21AI132910 and the Bill and Melinda Gates Foundation (OPP1206188).
Source: University of Arizona
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