Targeting blood-brain-barrier transcytosis – perspectives for drug delivery

Efficient transcytosis across the blood-brain-barrier (BBB) is an important strategy for accessing drug targets within the central nervous system (CNS). Despite extensive research the number of studies reporting successful delivery of macromolecules or macromolecular complexes to the CNS has remained very low. In order to expand current research it is important to know which receptors are selective and abundant on the BBB so that novel CNS-targeting antibodies or other ligands could be developed, targeting those receptors for transcytosis. To do that, we have set up a proteomics- and transcriptomics-based workflow within the COMPACT project (Collaboration on the Optimization of Macromolecular Pharmaceutical Access to Cellular Targets) of the Innovative Medicines Initiative (IMI) of the EU. Here we summarise our overall strategy in endothelial transcytosis research, describe in detail the related challenges, and discuss future perspectives of these studies. This article is part of the Special Issue entitled "Beyond small molecules for neurological disorders".

[1]  J. Elstrott,et al.  Transferrin receptor (TfR) trafficking determines brain uptake of TfR antibody affinity variants , 2014, The Journal of experimental medicine.

[2]  Robert Hoehndorf,et al.  Statistical Tests for Associations between Two Directed Acyclic Graphs , 2010, PloS one.

[3]  G. Lapin,et al.  Microvessel organization and structure in experimental brain tumors: microvessel populations with distinctive structural and functional properties. , 1999, Microvascular research.

[4]  Yu Zhou,et al.  Identifying blood-brain-barrier selective single-chain antibody fragments. , 2014, Biotechnology journal.

[5]  Carmel M Moran,et al.  Focused ultrasound as a non-invasive intervention for neurological disease: a review , 2016, British journal of neurosurgery.

[6]  W. Pardridge,et al.  Targeted delivery of protein and gene medicines through the blood–brain barrier , 2015, Clinical pharmacology and therapeutics.

[7]  B. Barres,et al.  The Mouse Blood-Brain Barrier Transcriptome: A New Resource for Understanding the Development and Function of Brain Endothelial Cells , 2010, PloS one.

[8]  M. Gumbleton,et al.  Peptide sequences mediating tropism to intact blood–brain barrier: An in vivo biodistribution study using phage display , 2012, Peptides.

[9]  T. Maniatis,et al.  An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex , 2014, The Journal of Neuroscience.

[10]  Maxime Culot,et al.  Modelling of the blood–brain barrier in drug discovery and development , 2007, Nature Reviews Drug Discovery.

[11]  E. Shusta,et al.  Targeting receptor-mediated transport for delivery of biologics across the blood-brain barrier. , 2015, Annual review of pharmacology and toxicology.

[12]  R. Watts,et al.  Developing Therapeutic Antibodies for Neurodegenerative Disease , 2013, Neurotherapeutics.

[13]  J. Tanha,et al.  Selection of phage‐displayed llama single‐domain antibodies that transmigrate across human blood‐brain barrier endothelium , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[14]  Peter C. Searson,et al.  The blood-brain barrier: an engineering perspective , 2013, Front. Neuroeng..

[15]  H. Duvernoy,et al.  The vascularization of the human cerebellar cortex , 1983, Brain Research Bulletin.

[16]  Bradley E. Enerson,et al.  The Rat Blood—Brain Barrier Transcriptome , 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[17]  R. Watts,et al.  Bispecific antibodies for delivery into the brain. , 2013, Current opinion in chemical biology.

[18]  T. Terasaki,et al.  Quantitative targeted proteomics for understanding the blood–brain barrier: towards pharmacoproteomics , 2014, Expert review of proteomics.

[19]  Charles Nicholson,et al.  Diffusion and related transport mechanisms in brain tissue , 2001 .

[20]  Anirvan Ghosh,et al.  Increased Brain Penetration and Potency of a Therapeutic Antibody Using a Monovalent Molecular Shuttle , 2014, Neuron.

[21]  E. Hansson,et al.  Astrocyte–endothelial interactions at the blood–brain barrier , 2006, Nature Reviews Neuroscience.

[22]  W. Pardridge Blood–brain barrier endogenous transporters as therapeutic targets: a new model for small molecule CNS drug discovery , 2015, Expert opinion on therapeutic targets.

[23]  Alessandra Bertoldo,et al.  Frequency and time-frequency analysis of intraoperative ECoG during awake brain stimulation , 2013, Front. Neuroeng..

[24]  中川 慎介 A new blood-brain barrier model using primary rat brain endothelial cells, pericytes and astrocytes , 2009 .

[25]  I. Jolliffe Principal Component Analysis , 2002 .

[26]  J. Pachter,et al.  Endothelial cell heterogeneity of blood‐brain barrier gene expression along the cerebral microvasculature , 2009, Journal of neuroscience research.

[27]  Melanie A. Huntley,et al.  Discovery of Novel Blood-Brain Barrier Targets to Enhance Brain Uptake of Therapeutic Antibodies , 2016, Neuron.

[28]  Nir Lipsman,et al.  Intracranial Applications of Magnetic Resonance-guided Focused Ultrasound , 2014, Neurotherapeutics.

[29]  M. Danhof,et al.  Drug transport across the blood-brain barrier , 1992, Pharmaceutisch Weekblad.

[30]  Ian T. Jolliffe,et al.  Principal Component Analysis , 2002, International Encyclopedia of Statistical Science.