Cargando…

Intravenous immunoglobulin prevents peripheral liver transduction of intrathecally delivered AAV vectors

Mostrar otras versiones (1)

Detalles Bibliográficos
Autores principales:	Horiuchi, Makoto, Hinderer, Christian J., Greig, Jenny A., Dyer, Cecilia, Buza, Elizabeth L., Bell, Peter, Chichester, Jessica A., Hayashi, Peter M., Yan, Hanying, Goode, Tamara, Wilson, James M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	American Society of Gene & Cell Therapy 2022
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668676/ https://www.ncbi.nlm.nih.gov/pubmed/36419470 http://dx.doi.org/10.1016/j.omtm.2022.11.001

Ejemplares similares

Intravenous immunoglobulin prevents peripheral liver transduction of intrathecally delivered AAV vectors
por: Horiuchi, Makoto, et al.
Publicado: (2022)

Translational Feasibility of Lumbar Puncture for Intrathecal AAV Administration
por: Hinderer, Christian, et al.
Publicado: (2020)

Impact of intravenous infusion time on AAV8 vector pharmacokinetics, safety, and liver transduction in cynomolgus macaques
por: Greig, Jenny A, et al.
Publicado: (2016)

Physical positioning markedly enhances brain transduction after intrathecal AAV9 infusion
por: Castle, Michael J., et al.
Publicado: (2018)

Efficacy of AAV serotypes to target Schwann cells after intrathecal and intravenous delivery
por: Kagiava, A., et al.
Publicado: (2021)

Safety and Efficacy of Intravenous and Intrathecal Delivery of AAV9-Mediated ARSA in Minipigs
por: Mullagulova, Aysilu, et al.
Publicado: (2023)

Evaluating the transduction efficiency of systemically delivered AAV vectors in the rat nervous system
por: Yang, Olivia J., et al.
Publicado: (2023)

Pilot Study Assessing the Impact of Intrathecal Administration of Variants AAV-PHP.B and AAV-PHP.eB on Brain Transduction in Adult Rhesus Macaques
por: Arotcarena, Marie-Laure, et al.
Publicado: (2021)

Toxicology Study of Intra-Cisterna Magna Adeno-Associated Virus 9 Expressing Iduronate-2-Sulfatase in Rhesus Macaques
por: Hordeaux, Juliette, et al.
Publicado: (2018)

Toxicology Study of Intra-Cisterna Magna Adeno-Associated Virus 9 Expressing Human Alpha-L-Iduronidase in Rhesus Macaques
por: Hordeaux, Juliette, et al.
Publicado: (2018)

Adeno‐associated virus serotype 1‐based gene therapy for FTD caused by GRN mutations
por: Hinderer, Christian, et al.
Publicado: (2020)

Biodistribution of adeno-associated virus serotype 9 (AAV9) vector after intrathecal and intravenous delivery in mouse
por: Schuster, Daniel J., et al.
Publicado: (2014)

Syngeneic AAV Pseudo-particles Potentiate Gene Transduction of AAV Vectors
por: Wang, Qizhao, et al.
Publicado: (2016)

AAV8 Gene Therapy for Crigler-Najjar Syndrome in Macaques Elicited Transgene T Cell Responses That Are Resident to the Liver
por: Greig, Jenny A., et al.
Publicado: (2018)

Successful Transduction with AAV Vectors after Selective Depletion of Anti-AAV Antibodies by Immunoadsorption
por: Orlowski, Alejandro, et al.
Publicado: (2020)

Prednisolone reduces the interferon response to AAV in cynomolgus macaques and may increase liver gene expression
por: Wang, Lili, et al.
Publicado: (2022)

Development of Intrathecal AAV9 Gene Therapy for Giant Axonal Neuropathy
por: Bailey, Rachel M., et al.
Publicado: (2018)

Global CNS Gene Delivery and Evasion of Anti-AAV Neutralizing Antibodies by Intrathecal AAV Administration in Non-Human Primates
por: Gray, Steven J., et al.
Publicado: (2013)

AAV-mediated photoreceptor transduction of the pig cone-enriched retina
por: Mussolino, C, et al.
Publicado: (2011)

Polymers for Improving the In Vivo Transduction Efficiency of AAV2 Vectors
por: Moulay, Gilles, et al.
Publicado: (2010)

Role of Essential Metal Ions in AAV Vector-Mediated Transduction
por: Rambhai, Himanshu K., et al.
Publicado: (2020)

Peripapillary Intravitreal Injection Improves AAV-Mediated Retinal Transduction
por: Madrakhimov, Sanjar Batirovich, et al.
Publicado: (2020)

An AAV capsid increases transduction of striatum and a ChAT promoter allows selective cholinergic neuron transduction
por: Santoscoy, Miguel C., et al.
Publicado: (2023)

Preferred transduction with AAV8 and AAV9 via thalamic administration in the MPS IIIB model: A comparison of four rAAV serotypes
por: Gilkes, J.A., et al.
Publicado: (2015)

Intranasal gene therapy to prevent infection by SARS-CoV-2 variants
por: Sims, Joshua J., et al.
Publicado: (2021)

Robust Long-term Transduction of Common Marmoset Neuromuscular Tissue With rAAV1 and rAAV9
por: Okada, Hironori, et al.
Publicado: (2013)

Direct Interaction of Human Serum Proteins with AAV Virions to Enhance AAV Transduction: Immediate Impact on Clinical Applications
por: Wang, Mei, et al.
Publicado: (2016)

Standard screening methods underreport AAV-mediated transduction and gene editing
por: Lang, Jonathan F., et al.
Publicado: (2019)

Rationally Engineered AAV Capsids Improve Transduction and Volumetric Spread in the CNS
por: Kanaan, Nicholas M., et al.
Publicado: (2017)

Intravenous Immunoglobulin Treatment Did Not Improve Tics in a Patient With Gilles de la Tourette Syndrome and Intrathecal Antibody Synthesis
por: Szejko, Natalia, et al.
Publicado: (2020)

Effects of Natalizumab Therapy on Intrathecal Immunoglobulin G Production Indicate Targeting of Plasmablasts
por: Schlüter, Miriam, et al.
Publicado: (2021)

CNS Transduction Benefits of AAV-PHP.eB over AAV9 Are Dependent on Administration Route and Mouse Strain
por: Mathiesen, Sophie N., et al.
Publicado: (2020)

Efficient gene transduction in pigs and macaques with the engineered AAV vector AAV.GT5 for hemophilia B gene therapy
por: Kashiwakura, Yuji, et al.
Publicado: (2023)

Intrathecal Administration of High-Titer Cytomegalovirus Immunoglobulin for Cytomegalovirus Meningitis
por: Fujiwara, Shin-ichiro, et al.
Publicado: (2014)

Widespread gene transfer in the central nervous system of cynomolgus macaques following delivery of AAV9 into the cisterna magna
por: Hinderer, Christian, et al.
Publicado: (2014)

Peptide Ligands Incorporated into the Threefold Spike Capsid Domain to Re-Direct Gene Transduction of AAV8 and AAV9 In Vivo
por: Michelfelder, Stefan, et al.
Publicado: (2011)

Glycosidic enzymes enhance retinal transduction following intravitreal delivery of AAV2
por: Cehajic-Kapetanovic, Jasmina, et al.
Publicado: (2011)

Capsid Serotype and Timing of Injection Determines AAV Transduction in the Neonatal Mice Brain
por: Chakrabarty, Paramita, et al.
Publicado: (2013)

AAV2-Mediated Transduction of the Mouse Retina After Optic Nerve Injury
por: Nickells, Robert W., et al.
Publicado: (2017)

Experimental Variables that Affect Human Hepatocyte AAV Transduction in Liver Chimeric Mice
por: Zou, Chenhui, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_velkdur8o6p9rm7af9b7dk1e0o