Homogeneous antibody-angiopep 2 conjugates for effective brain targeting.
Yasuaki AnamiWei XiongAiko YamaguchiChisato M YamazakiNingyan ZhangZhiqiang AnKyoji TsuchikamaPublished in: RSC advances (2022)
Antibody-based therapy has shown great success in the treatment of many diseases, including cancers. While antibodies and antibody-drug conjugates (ADCs) have also been evaluated for central nervous system (CNS) disorders as well as brain tumors, their therapeutic efficacy can be substantially limited due to low permeability across the blood-brain barrier (BBB). Thus, improving BBB permeability of therapeutic antibodies is critical in establishing this drug class as a reliable clinical option for CNS diseases. Here, we report that, compared with a conventional heterogeneous conjugation, homogeneous conjugation of the synthetic BBB shuttle peptide angiopep-2 (Ang2) to a monoclonal antibody (mAb) provides improved binding affinity for brain microvascular endothelial cells in vitro and accumulation into normal brain tissues in vivo . In a mouse model, we also demonstrate that the homogeneous anti-EGFR mAb-Ang2 conjugate administered intravenously efficiently accumulates in intracranial tumors. These findings suggest that homogeneous conjugation of BBB shuttle peptides such as Ang2 is a promising approach to enhancing the therapeutic efficacy of antibody agents for CNS diseases.
Keyphrases
- blood brain barrier
- monoclonal antibody
- cerebral ischemia
- endothelial cells
- resting state
- angiotensin ii
- white matter
- cancer therapy
- mouse model
- functional connectivity
- small cell lung cancer
- gene expression
- epidermal growth factor receptor
- emergency department
- multiple sclerosis
- brain injury
- young adults
- tyrosine kinase
- mesenchymal stem cells
- mass spectrometry
- adverse drug
- optic nerve