Researchers develop scalable method to generate key immune cells for cancer therapy
Researchers at the Center for Regenerative Medicine (CReM) at Boston Medical Center (BMC) and Boston University (BU) have developed a scalable method for generating CD4+ helper T cells from induced pluripotent stem cells (iPSCs), overcoming a longstanding challenge in the development of stem cell-based immunotherapies. The findings, published in Stem Cell Reports, could help advance efforts to…
Researchers at the Center for Regenerative Medicine (CReM) in Boston have created a method to efficiently produce CD4+ helper T cells from induced pluripotent stem cells (iPSCs). This breakthrough could lead to widely available, off-the-shelf CAR-T cell therapies for treating various types of cancer. Currently, each patient's CAR-T therapy is costly and time-consuming due to the need for personalized production. iPSCs, derived from adult skin or blood cells, could revolutionize the process by enabling large-scale, ready-to-use T cell production.
The challenge has been generating functional CD4+ helper T cells through a key molecular signaling pathway called Notch. Researchers discovered that by removing Notch signaling during later T cell maturation stages while simultaneously reducing anti-T cell receptor signaling, they could successfully produce CD4+ T cells in large quantities.
The team's protocol is simple, efficient, and scalable, paving the way for more accessible and affordable cancer treatments.
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