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In vivo generated human CAR T cells eradicate tumor cells

Oncoimmunology, 2019-12, Vol.8 (12), p.e1671761-e1671761

2019

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Receptor-Targeted Nipah Virus Glycoproteins Improve Cell-Type Selective Gene Delivery and Reveal a Preference for Membrane-Proximal Cell Attachment

PLoS pathogens, 2016-06, Vol.12 (6), p.e1005641-e1005641

2016

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In vivo CAR T cell therapy against angioimmunoblastic T cell lymphoma

Journal of experimental & clinical cancer research, 2024-09, Vol.43 (1), p.262-18, Article 262

2024

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A Two-Phase Expansion Protocol Combining Interleukin (IL)-15 and IL-21 Improves Natural Killer Cell Proliferation and Cytotoxicity against Rhabdomyosarcoma

Frontiers in immunology, 2017-06, Vol.8, p.676-676

2017

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CD62L as target receptor for specific gene delivery into less differentiated human T lymphocytes

Frontiers in immunology, 2023-08, Vol.14, p.1183698

2023

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Tumor-Specific Delivery of Immune Checkpoint Inhibitors by Engineered AAV Vectors

Frontiers in oncology, 2019-02, Vol.9, p.52-52

2019

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APPsα rescues CDK5 and GSK3β dysregulation and restores normal spine density in Tau transgenic mice

Frontiers in cellular neuroscience, 2023-01, Vol.17, p.1106176-1106176

2023

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CD19 and CD20 targeted vectors induce minimal activation of resting B lymphocytes

PloS one, 2013-11, Vol.8 (11), p.e79047-e79047

2013

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Immunization of mice with lentiviral vectors targeted to MHC class II+ cells is due to preferential transduction of dendritic cells in vivo

PloS one, 2014-07, Vol.9 (7), p.e101644-e101644

2014

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Surface-Engineered Viral Vectors for Selective and Cell Type-Specific Gene Delivery

Trends in biotechnology (Regular ed.), 2015-12, Vol.33 (12), p.777-790

2015

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Quantitative assays reveal cell fusion at minimal levels of SARS-CoV-2 spike protein and fusion from without

iScience, 2021-03, Vol.24 (3), p.102170-102170, Article 102170

2021

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Measles virus glycoprotein-based lentiviral targeting vectors that avoid neutralizing antibodies

PloS one, 2012-10, Vol.7 (10), p.e46667-e46667

2012

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CAR Gene Delivery by T‐cell Targeted Lentiviral Vectors is Enhanced by Rapamycin Induced Reduction of Antiviral Mechanisms

Advanced science, 2023-12, Vol.10 (35), p.e2302992-n/a

2023

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Chimäre Antigenrezeptoren (CARs) in der Onkologie: eine Übersicht zu klinischer Anwendung und neuen Entwicklungen

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2020, Vol.63 (11), p.1331-1340

2020

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Selective lentiviral gene delivery to CD133-expressing human glioblastoma stem cells

PloS one, 2014-12, Vol.9 (12), p.e116114-e116114

2014

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Receptor-targeted lentiviral vectors are exceptionally sensitive toward the biophysical properties of the displayed single-chain Fv

Protein engineering, design and selection, 2015-04, Vol.28 (4), p.93-106

2015

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Displaying Tetra‐Membrane Spanning Claudins on Enveloped Virus‐Like Particles for Cancer Immunotherapy

Biotechnology journal, 2018-03, Vol.13 (3), p.e1700345-n/a

2018

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Proceedings From the First International Workshop at Sidra Medicine: “Engineered Immune Cells in Cancer Immunotherapy (EICCI): From Discovery to Off-the-Shelf Development”, 15th–16th February 2019, Doha, Qatar

Frontiers in immunology, 2021-01, Vol.11, p.589381-589381

2021

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The Receptor Attachment Function of Measles Virus Hemagglutinin Can Be Replaced with an Autonomous Protein That Binds Her2/neu While Maintaining Its Fusion-Helper Function

Journal of Virology, 2013-06, Vol.87 (11), p.6246-6256

2013

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A new age of precision gene therapy

The Lancet (British edition), 2024-02, Vol.403 (10426), p.568-582

2024

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Enhancing the Oncolytic Activity of CD133-Targeted Measles Virus: Receptor Extension or Chimerism with Vesicular Stomatitis Virus Are Most Effective

Frontiers in oncology, 2017-06, Vol.7, p.127-127

2017

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Expansion of T memory stem cells with superior anti-tumor immunity by Urolithin A-induced mitophagy

Immunity (Cambridge, Mass.), 2022-11, Vol.55 (11), p.2059-2073.e8

2022

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Ligand Coupling to the AAV Capsid for Cell-Specific Gene Transfer

Methods in molecular biology (Clifton, N.J.), 2019, Vol.1950, p.35

2019

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Viral gene transfer of APPsα rescues synaptic failure in an Alzheimer’s disease mouse model

Acta neuropathologica, 2016-02, Vol.131 (2), p.247-266

2016

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Off-target-free gene delivery by affinity-purified receptor-targeted viral vectors

Nature communications, 2015-02, Vol.6 (1), p.6246-6246, Article 6246

2015

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In vivo generated human CAR T cells eradicate tumor cells

Receptor-Targeted Nipah Virus Glycoproteins Improve Cell-Type Selective Gene Delivery and Reveal a Preference for Membrane-Proximal Cell Attachment

In vivo CAR T cell therapy against angioimmunoblastic T cell lymphoma

A Two-Phase Expansion Protocol Combining Interleukin (IL)-15 and IL-21 Improves Natural Killer Cell Proliferation and Cytotoxicity against Rhabdomyosarcoma

CD62L as target receptor for specific gene delivery into less differentiated human T lymphocytes

Tumor-Specific Delivery of Immune Checkpoint Inhibitors by Engineered AAV Vectors

APPsα rescues CDK5 and GSK3β dysregulation and restores normal spine density in Tau transgenic mice

CD19 and CD20 targeted vectors induce minimal activation of resting B lymphocytes

Immunization of mice with lentiviral vectors targeted to MHC class II+ cells is due to preferential transduction of dendritic cells in vivo

Surface-Engineered Viral Vectors for Selective and Cell Type-Specific Gene Delivery

Quantitative assays reveal cell fusion at minimal levels of SARS-CoV-2 spike protein and fusion from without

Measles virus glycoprotein-based lentiviral targeting vectors that avoid neutralizing antibodies

CAR Gene Delivery by T‐cell Targeted Lentiviral Vectors is Enhanced by Rapamycin Induced Reduction of Antiviral Mechanisms

Chimäre Antigenrezeptoren (CARs) in der Onkologie: eine Übersicht zu klinischer Anwendung und neuen Entwicklungen

Selective lentiviral gene delivery to CD133-expressing human glioblastoma stem cells

Receptor-targeted lentiviral vectors are exceptionally sensitive toward the biophysical properties of the displayed single-chain Fv

Displaying Tetra‐Membrane Spanning Claudins on Enveloped Virus‐Like Particles for Cancer Immunotherapy

Proceedings From the First International Workshop at Sidra Medicine: “Engineered Immune Cells in Cancer Immunotherapy (EICCI): From Discovery to Off-the-Shelf Development”, 15th–16th February 2019, Doha, Qatar

The Receptor Attachment Function of Measles Virus Hemagglutinin Can Be Replaced with an Autonomous Protein That Binds Her2/neu While Maintaining Its Fusion-Helper Function

A new age of precision gene therapy

Enhancing the Oncolytic Activity of CD133-Targeted Measles Virus: Receptor Extension or Chimerism with Vesicular Stomatitis Virus Are Most Effective

Expansion of T memory stem cells with superior anti-tumor immunity by Urolithin A-induced mitophagy

Ligand Coupling to the AAV Capsid for Cell-Specific Gene Transfer

Viral gene transfer of APPsα rescues synaptic failure in an Alzheimer’s disease mouse model

Off-target-free gene delivery by affinity-purified receptor-targeted viral vectors

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