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Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors

https://doi.org/10.1038/gt.2008.186
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/glia.10195openalex-snapshot
Lentiviral vectors for gene delivery to normal and demyelinated white matter
inferredcites →https://doi.org/10.1002/jnr.10719openalex-snapshot
Targeted transgene expression in rat brain using lentiviral vectors
inferredcites →https://doi.org/10.1006/exnr.1999.7178openalex-snapshot
Lentiviral Gene Transfer to the Nonhuman Primate Brain
inferredcites →https://doi.org/10.1006/exnr.2002.7977openalex-snapshot
Grafts of BDNF-Producing Fibroblasts Rescue Axotomized Rubrospinal Neurons and Prevent Their Atrophy
inferredcites →https://doi.org/10.1016/j.brainres.2004.07.030openalex-snapshot
Late onset neurodegeneration in the Cln3−/− mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation
inferredcites →https://doi.org/10.1016/j.modgep.2007.05.004openalex-snapshot
Neogenin is expressed on neurogenic and gliogenic progenitors in the embryonic and adult central nervous system
inferredcites →https://doi.org/10.1016/j.nbd.2004.02.010openalex-snapshot
Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 null mutant mouse model of infantile neuronal ceroid lipofuscinosis
inferredcites →https://doi.org/10.1016/j.nbd.2005.05.018openalex-snapshot
Thalamocortical neuron loss and localized astrocytosis in the Cln3Δex7/8 knock-in mouse model of Batten disease
inferredcites →https://doi.org/10.1016/j.nbd.2006.09.001openalex-snapshot
Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis
inferredcites →https://doi.org/10.1016/j.ymthe.2003.09.017openalex-snapshot
Transduction Patterns of Pseudotyped Lentiviral Vectors in the Nervous System
inferredcites →https://doi.org/10.1016/j.ymthe.2005.11.012openalex-snapshot
Lentiviral Vectors for Use in the Central Nervous System
inferredcites →https://doi.org/10.1038/nm1365openalex-snapshot
Effective gene therapy with nonintegrating lentiviral vectors
inferredcites →https://doi.org/10.1038/sj.gt.3302440openalex-snapshot
A lentiviral vector encoding the human Wiskott–Aldrich syndrome protein corrects immune and cytoskeletal defects in WASP knockout mice
inferredcites →https://doi.org/10.1038/sj.gt.3302632openalex-snapshot
Gene Therapy Progress and Prospects: Fetal gene therapy – first proofs of concept – some adverse effects
inferredcites →https://doi.org/10.1038/sj.gt.3302924openalex-snapshot
Efficient gene transduction of neurons by lentivirus with enhanced neuron-specific promoters
inferredcites →https://doi.org/10.1056/nejm200301163480314openalex-snapshot
A Serious Adverse Event after Successful Gene Therapy for X-Linked Severe Combined Immunodeficiency
inferredcites →https://doi.org/10.1073/pnas.0606197103openalex-snapshot
Lentiviral vectors with a defective integrase allow efficient and sustained transgene expression in vitro and in vivo
inferredcites →https://doi.org/10.1073/pnas.93.21.11382openalex-snapshot
Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector.
inferredcites →https://doi.org/10.1089/hum.2006.17.1openalex-snapshot
Lentivirus-Mediated Gene Transfer to the Central Nervous System: Therapeutic and Research Applications
inferredcites →https://doi.org/10.1089/hum.2007.013openalex-snapshot
Use of Nonintegrating Lentiviral Vectors for Gene Therapy
inferredcites →https://doi.org/10.1093/hmg/10.19.2109openalex-snapshot
Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery
inferredcites →https://doi.org/10.1093/hmg/ddl251openalex-snapshot
Lentiviral vector expressing retinoic acid receptor β2 promotes recovery of function after corticospinal tract injury in the adult rat spinal cord
inferredcites →https://doi.org/10.1097/brs.0b013e318053ec35openalex-snapshot
Brain-Derived Neurotrophic Factor Gene Transfer With Adeno-Associated Viral and Lentiviral Vectors Prevents Rubrospinal Neuronal Atrophy and Stimulates Regeneration-Associated Gene Expression After Acute Cervical Spinal Cord Injury
inferredcites →https://doi.org/10.1126/science.1088547openalex-snapshot
LMO2 -Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1
inferredcites →https://doi.org/10.1128/jvi.01865-08openalex-snapshot
Insertional Gene Activation by Lentiviral and Gammaretroviral Vectors
inferredcites →https://doi.org/10.1128/jvi.71.9.6641-6649.1997openalex-snapshot
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector
inferredcites →https://doi.org/10.1128/jvi.72.11.8861-8872.1998openalex-snapshot
Effect of Host Modification and Age on Airway Epithelial Gene Transfer Mediated by a Murine Leukemia Virus-Derived Vector
inferredcites →https://doi.org/10.1128/jvi.77.10.5902-5910.2003openalex-snapshot
Lentivirus Vectors Pseudotyped with Filoviral Envelope Glycoproteins Transduce Airway Epithelia from the Apical Surface Independently of Folate Receptor Alpha
inferredcites →https://doi.org/10.1128/mcb.26.10.3764-3772.2006openalex-snapshot
Cortical Thinning and Hydrocephalus in Mice Lacking the Immunoglobulin Superfamily Member CDO
inferredcites →https://doi.org/10.1182/blood-2005-10-4108openalex-snapshot
Acute myeloid leukemia is associated with retroviral gene transfer to hematopoietic progenitor cells in a rhesus macaque

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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In Utero Gene Therapy and its Application in Genetic Hearing Loss
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Local transgene expression and whole‐body transgenesis to model brain diseases in nonhuman primate
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Lentiviral vectors encoding short hairpin RNAs efficiently transduce and knockdown LINGO‐1 but induce an interferon response and cytotoxicity in central nervous system neurones
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Fetal gene therapy
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Vector Tropism
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Lentiviral Vectors for Gene Delivery to the Nervous System
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Cell Type-Specific Targeting Strategies for Optogenetics
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Integrase Defective, Nonintegrating Lentiviral Vectors
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Vector Systems for Prenatal Gene Therapy: Principles of Retrovirus Vector Design and Production
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Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects
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Current non-invasive strategies for brain drug delivery: overcoming blood–brain barrier transport
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Destination Brain: the Past, Present, and Future of Therapeutic Gene Delivery
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In vivo genome editing targeted towards the female reproductive system
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High Transgene Expression by Lentiviral Vectors Causes Maldevelopment of Purkinje Cells In Vivo
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Optogenetics Dissection of Sleep Circuits and Functions
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Future of Cellular and Molecular Diagnostics
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Viral vectors for gene delivery to the central nervous system
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Experimental therapies in the neuronal ceroid lipofuscinoses
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Lentivirus-mediated transfer of MMP-9 shRNA provides neuroprotection following focal ischemic brain injury in rats
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High-efficiency transduction of spinal cord motor neurons by intrauterine delivery of integration-deficient lentiviral vectors
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Lentiviral vector-mediated rescue of motor behavior in spontaneously occurring hereditary ataxic mice
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Viral vectors for gene delivery to the central nervous system
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Recent progress and challenges in gene therapy for pharmacoresistant focal epilepsy
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2017.05.029openalex-snapshot
Gene therapy and editing: Novel potential treatments for neuronal channelopathies
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Genetic therapies for neurological diseases
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Viral vectors for neurotrophic factor delivery: A gene therapy approach for neurodegenerative diseases of the CNS
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MuLV IN mutants responsive to HDAC inhibitors enhance transcription from unintegrated retroviral DNA
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Super-resolving Microscopy in Neuroscience
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Integrase-defective lentiviral vectors: progress and applications
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Ocular gene delivery using lentiviral vectors
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In utero administration of Ad5 and AAV pseudotypes to the fetal brain leads to efficient, widespread and long-term gene expression
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Corticospinal tract transduction: a comparison of seven adeno-associated viral vector serotypes and a non-integrating lentiviral vector
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Efficient gene expression from integration-deficient lentiviral vectors in the spinal cord
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Differences in vector-genome processing and illegitimate integration of non-integrating lentiviral vectors
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In utero delivery of rAAV2/9 induces neuronal expression of the transgene in the brain: towards new models of Parkinson’s disease
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Integration-deficient Lentiviral Vectors: A Slow Coming of Age
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Recent Advances in Lentiviral Vector Development and Applications
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Gene Delivery of a Mutant TGFβ3 Reduces Markers of Scar Tissue Formation After Cutaneous Wounding
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Assessment of Integration-defective HIV-1 and EIAV Vectors In Vitro and In Vivo
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CCR5 Gene Editing of Resting CD4+ T Cells by Transient ZFN Expression From HIV Envelope Pseudotyped Nonintegrating Lentivirus Confers HIV-1 Resistance in Humanized Mice
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Gene therapy in epilepsy—is it time for clinical trials?
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Bringing balance to the force–regulatable gene therapy for epilepsy
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Strategies for delivering therapeutics across the blood–brain barrier
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Fetal gene therapy for neurodegenerative disease of infants
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Continual conscious bioluminescent imaging in freely moving somatotransgenic mice
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Dysregulated Wnt and NFAT signaling in a Parkinson’s disease LRRK2 G2019S knock-in model
inferred← citeshttps://doi.org/10.1038/srep22824openalex-snapshot
Mechanical oscillations enhance gene delivery into suspended cells
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Current therapies for the soluble lysosomal forms of neuronal ceroid lipofuscinosis
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In utero gene transfer to the mouse nervous system
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Lentiviral Vector-Mediated RNA Silencing in the Central Nervous System
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Integrase-Deficient Lentiviral Vectors Mediate Efficient Gene Transfer to Human Vascular Smooth Muscle Cells with Minimal Genotoxic Risk
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Transgenic Expression of Human Glial Cell Line-Derived Neurotrophic Factor from Integration-Deficient Lentiviral Vectors is Neuroprotective in a Rodent Model of Parkinson's Disease
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Post-Injury Delivery of rAAV2-CNTF Combined with Short-Term Pharmacotherapy Is Neuroprotective and Promotes Extensive Axonal Regeneration after Optic Nerve Trauma
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Phoenix rising: gene therapy makes a comeback
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In utero therapy for spinal muscular atrophy: closer to clinical translation
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Genetic therapy for the nervous system
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Intravenous administration of AAV2/9 to the fetal and neonatal mouse leads to differential targeting of CNS cell types and extensive transduction of the nervous system
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Parkinson's Disease: Gene Therapies
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Viral transduction of the neonatal brain delivers controllable genetic mosaicism for visualising and manipulating neuronal circuits in vivo
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Recent progress in satellite cell/myoblast engraftment – relevance for therapy
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A Comparative Study of Transfection Efficiency between Liposomes, Immunoliposomes and Brain-specific Immunoliposomes
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LDLR-Gene therapy for familial hypercholesterolaemia: problems, progress, and perspectives
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Gene Therapy for Parkinson’s
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Optimization of Mucosal Responses after Intramuscular Immunization with Integrase Defective Lentiviral Vector
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Investigative and emerging treatments for Batten disease
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Transfection Techniques for Neuronal Cells: Table 1.
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Epilepsy Gene Therapy Using an Engineered Potassium Channel
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Factors affecting the formation, stability, and expression of unintegrated lentiviral vector genomes
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Insights into the mechanisms of HIV-1 cis elements and trans factors required for RNA encapsidation and transduction
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Use of HIV as a gene transfer vector.
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Emerging applications of lentiviral vectors in dendritic cell-based immunotherapy
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Gene delivery with viral vectors for cerebrovascular diseases
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Transgene expression in the mouse cerebellar Purkinje cells with a minimal level of integration using long terminal repeat–modified lentiviral vectors
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Anesthesia and analgesia for experimental craniotomy in mice and rats: a systematic scoping review comparing the years 2009 and 2019
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Non-Integrating Lentiviral Vectors in Clinical Applications: A Glance Through
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Design and Potential of Non-Integrating Lentiviral Vectors
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Gene Therapy for the Treatment of Parkinson’s Disease: The Nature of the Biologics Expands the Future Indications
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Drug Delivery to the Brain: Recent Advances and Unmet Challenges
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The Old and the New: Prospects for Non-Integrating Lentiviral Vector Technology
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Faculty Opinions recommendation of Fetal gene therapy for neurodegenerative disease of infants.
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Lentiviral vector-based therapy in head and neck cancer (Review)
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Gene Delivery Strategies to Promote Spinal Cord Repair
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Viral Vectors and Delivery Strategies for CNS Gene Therapy
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Perinatal Gene Delivery to the CNS
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NOSE TO BRAIN DELIVERY: ROLE OF VIRAL AND NON-VIRAL VECTORS FOR NEUROLOGICAL DISORDER
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Assessing the potential of non-integrating lentiviral vectors for cardiovascular gene therapy
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Designing Lentiviral Gene Vectors
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Stem Cell Based Therapy for Muscular Dystrophies: Cell Types and Environmental Factors Influencing Their Efficacy
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Nanoparticle (MPG)-mediated delivery of small RNAs into human mesenchymal stem cells
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Caractérisation de P42, région cruciale pour la fonction de la Huntingtine et peptide capable d’inhiber la toxicité associée à la Chorée de Huntington
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Novel regulation of neuronal genes implicated in Alzheimer disease by microRNA
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