Can immune cell ‘couriers’ deliver Alzheimer’s therapy?
- Researchers at University of California, Irvine have created “living cellular couriers” called microglia that can deliver disease-fighting proteins to specific areas of the brain, potentially improving treatment for Alzheimer’s disease and other neurological disorders.
- The microglia cells were engineered using CRISPR gene editing to secrete an enzyme that breaks down toxic proteins associated with Alzheimer’s disease, reducing inflammation and preserving neurons and synaptic connections.
- The study demonstrates that these engineered microglia can target specific brain changes, such as amyloid plaques, and release therapeutic agents only when needed, offering a highly targeted and safe treatment approach.
- The research also explored the potential of human microglia to treat other central nervous system diseases, including brain cancer and multiple sclerosis, highlighting the possibility of tailoring these cells to specific conditions.
A new way to deliver disease-fighting proteins throughout the brain may improve the treatment of Alzheimer’s disease and other neurological disorders, according to University of California, Irvine scientists.
By engineering human immune cells called microglia, the researchers have created living cellular “couriers” capable of responding to brain pathology and releasing therapeutic agents exactly where needed.
Microglia are immune cells that reside in the central nervous system, including the brain and spinal cord. They act as the brain’s primary line of defense against infection and injury, performing like white blood cells do elsewhere in the body.
Think of microglia as the brain’s own surveillance and cleanup crew. They constantly scan the brain for signs of trouble—like pathogens, damaged cells, or toxic proteins—and respond by engulfing and digesting harmful substances in a process called phagocytosis.
Microglia also help regulate inflammation and support neuronal function and plasticity during brain development and aging.
Importantly, in diseases like Alzheimer’s, microglia are found near amyloid plaques (clumps of toxic proteins), where they become activated and attempt to surround and clear this toxic debris. But in chronic disease, their activity can become dysregulated, contributing to neuroinflammation and further neuronal damage. Because of their central role in both protecting and sometimes harming the brain, microglia are a major focus of neurological research and a promising target for therapies.
The study in Cell Stem Cell demonstrates for the first time that microglia derived from induced pluripotent stem cells can be genetically programmed to detect disease-specific brain changes—like amyloid plaques in Alzheimer’s disease—and then release enzymes that help break down those toxic proteins.
As a result, the cells were able to reduce inflammation, preserve neurons and synaptic connections, and reverse multiple other hallmarks of neurodegeneration in mice.
For patients and families grappling with Alzheimer’s and related diseases, the findings offer a hopeful glimpse at a future in which microglial-based cell therapies could precisely and safely counteract the ravages of neurodegeneration.
“Delivering biologics to the brain has long been a major challenge because of the blood-brain barrier,” says Mathew Blurton-Jones, a University of California, Irvine professor of neurobiology and behavior and co-corresponding author on the study.
“We’ve developed a programmable, living delivery system that gets around that problem by residing in the brain itself and responding only when and where it’s needed.”
Using CRISPR gene editing, the team modified human microglia to secrete neprilysin—an enzyme known to degrade beta-amyloid—under the control of a promoter that only activates near plaques. The result was a highly targeted and pathology-responsive therapy. In Alzheimer’s mouse models, these engineered microglia reduced the buildup of beta-amyloid and protected against damage to neurons and synapses, curbed inflammation, and even lowered a biomarker of neuronal injury in the blood.
“Remarkably, we found that placing the microglia in specific brain areas could reduce toxic amyloid levels and other AD-associated neuropathologies throughout the brain,” says Jean Paul Chadarevian, a postdoctoral scholar in the Blurton-Jones lab and first author on the study.
“And because the therapeutic protein was only produced in response to amyloid plaques, this approach was highly targeted yet broadly effective.”
In addition to Alzheimer’s, the research explored how human microglia respond in models of brain cancer and multiple sclerosis. In both cases, the engineered cells adopted unique gene expression profiles—highlighting the potential to tailor them to a variety of central nervous system diseases.
“This work opens the door to a completely new class of brain therapies,” says Robert Spitale, a professor of pharmaceutical sciences and co-corresponding author on the study.
“Instead of using synthetic drugs or viral vectors, we’re enlisting the brain’s immune cells as precision delivery vehicles.”
The researchers note that much work remains to translate this platform into human trials, including demonstrating long-term safety and developing methods for scalable manufacturing. However, because the microglia are derived from induced pluripotent stem cells, they could possibly be produced from a patient’s own cells, reducing the risk of immune rejection.
Grants from the National Institute on Aging, the California Institute for Regenerative Medicine, and Cure Alzheimer’s Fund supported the research.
Source: UC Irvine
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