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Current and Emerging Strategies for Enhancing Antibody Delivery to the Brain.

Authors: Bajracharya R, Caruso AC, Vella LJ, Nisbet RM

For the treatment of neurological diseases, achieving sufficient exposure to the brain parenchyma is a critical determinant of drug efficacy. The blood-brain barrier (BBB) functions to tightly control the passage of substances between the bloodstream and the central nervous system, and as such poses a major obstacle that must be overcome for therapeutics to enter the brain. Monoclonal antibodies have emerged as one of the best-selling treatment modalities available in the pharmaceutical market owing to their high target specificity. However, it has been estimated that only 0.1% of peripherally administered antibodies can cross the BBB, contributing to the low success rate of immunotherapy seen in clinical trials for the treatment of neurological diseases. The development of new strategies for antibody delivery across the BBB is thereby crucial to improve immunotherapeutic efficacy. Here, we discuss the current strategies that have been employed to enhance antibody delivery across the BBB. These include (i) focused ultrasound in combination with microbubbles, (ii) engineered bi-specific antibodies, and (iii) nanoparticles. Furthermore, we discuss emerging strategies such as extracellular vesicles with BBB-crossing properties and vectored antibody genes capable of being encapsulated within a BBB delivery vehicle.

Introduction

Purpose Drug delivery with BBB opening
Study Objective To review current and emerging strategies for enhancing monoclonal antibody delivery across the blood–brain barrier.
Animal model / Human subject None.
Disease model neurological diseases
Cargo name and characteristics Monoclonal antibodies — protein therapeutics with high target specificity but very low natural BBB penetration (~0.1% of peripheral dose). The paper discusses engineered bispecific antibodies (to engage BBB transport receptors), delivery via nanoparticles or extracellular vesicles (nanoparticle/extracellular vesicle vehicles), and vectored antibody genes (viral vector/AAV-style gene delivery for in vivo antibody expression).
Route of administration Peripheral (systemic) administration — e.g., intravenous

Outcomes and Safety

Summary of Outcomes Various techniques—including focused ultrasound with microbubbles, engineered bispecific antibodies, nanoparticles, extracellular vesicles, and vectored antibody genes—enhance delivery of therapeutic antibodies across the blood–brain barrier, increasing brain parenchymal exposure.
Safety-related matter No safety concerns or adverse effects are mentioned in the provided text.

Brain Region

Visualization unavailable

Ultrasound Parameters

Ultrasound instrument None.
FUS Mode pulsed
Duration of a single FUS session None.

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