Gene Therapy Researchers Find Viral Barcode to Cross the Blood-Brain Barrier

Summary: Researchers have identified structures that allow certain virus vectors to reach the brain easily.

Source: UNC.

Gene therapies promise to revolutionize the treatment of many diseases, including neurological diseases such as ALS. But the small viruses that deliver therapeutic genes can have adverse side effects at high doses. UNC School of Medicine researchers have now found a structure on these viruses that makes them better at crossing from the bloodstream into the brain – a key factor for administering gene therapies at lower doses for treating brain and spinal disorders.

“This structural ‘footprint’ we found seems to help these viruses get efficiently into the brain, which informs the design of potentially safer brain-targeted gene therapies,” said study senior author Aravind Asokan, PhD, associate professor of genetics.

The study, published in Molecular Therapy, examined adeno-associated viruses (AAVs), the most commonly used virus vectors for delivering gene therapies. The natural forms of these small viruses normally infect people without causing disease. For gene therapies, scientists remove most of the AAV genome, replace it with therapeutic genetic cargo, and inject trillions of copies into the patient.

In principle, scientists can modify AAVs to infect some cell types more than others to deliver their therapeutic payloads where they are most needed. However, most AAVs cannot easily cross from the bloodstream into the brain. Like most other viruses, they tend to be blocked by the cells that tightly line brain capillaries to form the so-called blood-brain barrier.

“To achieve therapeutic effects in the brain, AAVs sometimes have to be given in high doses, which raises the possibility of dose-dependent toxicity,” said first author Blake Albright, a graduate research assistant at UNC.

For the study, Albright, Asokan and colleagues tried to isolate the features that enable AAVs to cross the blood-brain barrier more easily. They started with two known AAVs, one that doesn’t efficiently cross the blood-brain barrier, and one that does. They created a small library of new variants of these AAVs by swapping short stretches of DNA from one to the other. They then tested these for their ability to cross the blood-brain barrier in mice.

In this way they isolated a closely spaced set of just eight amino acids on the viral coating that confers the ability to cross the blood-brain barrier efficiently. “Grafting that structural footprint onto another AAV strain enables it to cross into the brain much more easily,” Albright said.

The finding suggests that other AAVs used for a gene therapy targeting the brain or spinal cord might be improved by having the same or a similar set of amino acids. It would cross the blood-brain barrier more efficiently, and thus in principle would require a smaller dose to achieve therapeutic effects in the brain.

A smaller AAV dose would in itself mean a smaller chance of adverse side effects. But the UNC scientists found another potential safety benefit. Compared to their parental strains, AAV variants containing the key set of amino acids were less likely to get into other, non-brain cells, including liver cells. Transient liver toxicity is a significant concern in gene therapy when high doses are required.

pyramidal neurons
This image shows AAV therapy affecting pyramidal neurons in the hippocampus. image is credited to Blake Albright, Asokan Lab.

“We also found that our AAV variants containing this key amino acid footprint preferentially get into neurons rather than other brain cell types,” Asokan said. “This could be particularly useful for some gene therapies that target the brain.”

Gene therapies against neurological diseases are under investigation in clinical and preclinical trials, and include therapies for ALS, Huntington’s disease, Spinal Muscular Atrophy, Friedrich’s ataxia, and other disorders.

The UNC researchers are now trying to determine the precise molecular details of how the set of AAV amino acids allows the viruses to cross the blood-brain barrier. They are also studying how structures that enable blood-brain barrier crossing might differ from one animal species to another.

About this neuroscience research article

Funding: The National Institutes of Health funded this work.

Source: Mark Derewicz – UNC
Publisher: Organized by
Image Source: image is credited to Blake Albright, Asokan Lab.
Original Research: Abstract in Molecular Therapy.

Cite This Article

[cbtabs][cbtab title=”MLA”]UNC “Gene Therapy Researchers Find Viral Barcode to Cross the Blood-Brain Barrier.” NeuroscienceNews. NeuroscienceNews, 10 February 2018.
<>.[/cbtab][cbtab title=”APA”]UNC (2018, February 10). Gene Therapy Researchers Find Viral Barcode to Cross the Blood-Brain Barrier. NeuroscienceNews. Retrieved February 10, 2018 from[/cbtab][cbtab title=”Chicago”]UNC “Gene Therapy Researchers Find Viral Barcode to Cross the Blood-Brain Barrier.” (accessed February 10, 2018).[/cbtab][/cbtabs]


Mapping the Structural Determinants Required for AAVrh.10 Transport across the Blood-Brain Barrier

Effective gene delivery to the CNS by intravenously administered adeno-associated virus (AAV) vectors requires crossing the blood-brain barrier (BBB). To achieve therapeutic CNS transgene expression, high systemic vector doses are often required, which poses challenges such as scale-up costs and dose-dependent hepatotoxicity. To improve the specificity and efficiency of CNS gene transfer, a better understanding of the structural features that enable AAV transit across the BBB is needed. We generated a combinatorial domain swap library using AAV1, a serotype that does not traverse the vasculature, and AAVrh.10, which crosses the BBB in mice. We then screened individual variants by phylogenetic and structural analyses and subsequently conducted systemic characterization in mice. Using this approach, we identified key clusters of residues on the AAVrh.10 capsid that enabled transport across the brain vasculature and widespread neuronal transduction in mice. Through rational design, we mapped a minimal footprint from AAVrh.10, which, when grafted onto AAV1, confers the aforementioned CNS phenotype while diminishing vascular and hepatic transduction through an unknown mechanism. Functional mapping of this capsid surface footprint provides a roadmap for engineering synthetic AAV capsids for efficient CNS gene transfer with an improved safety profile.

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