Sneaking past the blood-brain barrier to usher in the age of gene therapy for neurodegenerative disease

In a paper titled "BBB opening with focused ultrasound in nonhuman primates and Parkinson's disease patients: Targeted AAV vector delivery and PET imaging," published inScience Advances, researchers led by the University CEU-San Pablo in Spain report on a method of safely traversing the blood-brain barrier.

神经退行性疾病如帕金森症,Alzheimer's and Huntington's disease have no cure or therapy options to slow their progression. Potentially promising therapy options have been proposed but are limited by the inability to cross the blood-brain barrier.

Gene therapy is one of the potential therapies that researchers would like to study, with the hope of correcting pathogenic mechanisms, bolstering neuroprotection, and initiating neuroregeneration and restoration of damagedbrain tissue.

Adeno-associated virus (AAV) vectors are an attractive vehicle for transferringgenesinto tissues. AAVs are small non-enveloped single-stranded DNA that scientists have been working on to create a platform for gene delivery. There are engineered AAVs with most of the viral genomes replaced with "expression cassettes" containing a promoter, a gene payload, and a terminator. These research AAVs cannot replicate like a wild virus, but the gene cargo they carry can be expressed (often with a second helper virus), providing long-term therapeutically beneficial gene expression.

An advantage ofgene therapyis that AAV vector delivery would only occasionally be needed as previous studies have shown treatments that last several years or more. Drug molecule therapies require much more frequent interventions, which is not usually a barrier to treatment unless that treatment is in the brain.

One limiting factor in using AAVs (or drug molecules) in the brain is the blood-brain barrier, a tight net of protective endothelial cells, pericytes, astrocytes and microglia all work to keep out bacteria and unwanted molecules while letting oxygen, carbon dioxide and water circulation occur.

To get past the barrier, AAVs must remain very small, limiting the cassette payload options. Once the AAVs make it past, another problem arises, location. If AAVs are needed to treat specific tissues in specific locations of the brain, just getting past the blood-brain may not be enough to generate the therapeutic effect.

In animal research models, the act of inserting AAVs with intracerebral injections, the most direct way of conducting a therapeutic genetic trial, can sometimes result in enough traumatic tissue damage to cause death. Reasonably, this is a limiting factor when consideringhuman trials. As the study authors point out, neurodegenerative disease treatments may require delivery into severalbrain regionssimultaneously and an idealgene deliveryapproach to brain diseases should be safe, noninvasive, and region-specific.

In the current study, researchers report creating a successful blood-brain barrier opening and delivering AAV vectors into specific brain regions involved in Parkinson's disease using low-intensity focus ultrasound guided by magnetic resonance imaging.

Neuronal green fluorescent protein expression was observed specifically in regions with the blood-brain barrier opening, confirming that the delivery method succeeded. Blood-brain barrier permeability was restored within 24 hours, and no adverse effects were reported.

The initial trial was conducted in adult macaque monkeys, and a follow-up was conducted on three human patients with Parkinson's disease. The less-invasive nature of this methodology could facilitate viral vector delivery for gene therapy making theoretical interventions to treat neurodegenerative disorders a reality.

While the current study focused on neurodegenerative disorders, a host of other ailments have evaded treatment because they take place behind theblood-brain barrierand are beyond the reach of conventional therapeutics. Meningitis, syphilis and toxoplasmosis, to name a few, could all see new treatment options with a safe passage across the labyrinth of protective brain vasculature.

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