Results 1 to 10 of about 115,363 (220)

Identification of a small molecule for enhancing lentiviral transduction of T cells [PDF]

open access: yesMolecular Therapy: Methods & Clinical Development, 2023
Genetic modification of cells using viral vectors has shown huge therapeutic benefit in multiple diseases. However, inefficient transduction contributes to the high cost of these therapies.
Paulina Malach   +10 more
doaj   +4 more sources

CD9 and folate receptor overexpression are not sufficient for VSV-G-independent lentiviral transduction. [PDF]

open access: yesPLoS ONE, 2022
Extracellular vesicles have become a research focus for their potential as therapeutic vehicles that carry cargo substances. Extracellular vesicles may origin from the endosomal compartment and share several characteristics with the envelope of ...
Cristina Bellotti   +2 more
doaj   +3 more sources

Systematic improvements in lentiviral transduction of primary human natural killer cells undergoing ex vivo expansion [PDF]

open access: yesMolecular Therapy: Methods & Clinical Development, 2021
Transduction of primary human natural killer (NK) cells with lentiviral vectors has historically been challenging. We sought to evaluate multiple parameters to optimize lentiviral transduction of human peripheral blood NK cells being expanded to large ...
David S.J. Allan   +6 more
doaj   +2 more sources

Hypoxia and HIF-1 inhibition enhance lentiviral transduction efficiency: a novel strategy for gene delivery optimization [PDF]

open access: yesBMC Biotechnology
Lentiviral vectors are widely used for stable gene delivery, but their transduction efficiency can be limited by suboptimal experimental conditions. Here, we investigated the role of oxygen concentration and hypoxia-inducible factor 1 (HIF-1) signaling ...
Qianyu Huo   +10 more
doaj   +2 more sources

High-Efficiency Lentiviral Transduction of Human CD34+ Cells in High-Density Culture with Poloxamer and Prostaglandin E2 [PDF]

open access: yesMolecular Therapy: Methods & Clinical Development, 2019
Hematopoietic stem cell (HSC) gene therapy is curative for various hereditary diseases; however, high-efficiency transduction in HSCs remains crucial to improve the prospects for hemoglobinopathies.
Naoya Uchida   +9 more
doaj   +2 more sources

Engineering fusogenic molecules to achieve targeted transduction of enveloped lentiviral vectors [PDF]

open access: goldJournal of Biological Engineering, 2009
Background Lentiviral vectors with broad tropism are one of the most promising gene delivery systems capable of efficiently delivering genes of interest into both dividing and non-dividing cells while maintaining long-term transgene expression.
Wang Pin, Joo Kye-Il, Lei Yuning
doaj   +2 more sources

A Nontoxic Transduction Enhancer Enables Highly Efficient Lentiviral Transduction of Primary Murine T Cells and Hematopoietic Stem Cells [PDF]

open access: yesMolecular Therapy: Methods & Clinical Development, 2018
Lentiviral vectors have emerged as an efficient, safe therapeutic tool for gene therapy based on hematopoietic stem cells (HSCs) or T cells. However, the monitoring of transduced cells in preclinical models remains challenging because of the inefficient ...
Marianne Delville   +8 more
doaj   +2 more sources

The effect of enhancers on the lentiviral transduction efficiency in the human RPE cells: Insights for advancing retinal gene therapies [PDF]

open access: yesBiochemistry and Biophysics Reports
Background: Viral vectors including lentiviruses (LV), adenoviruses (AV) and adeno-associated viruses (AAV) have been used as common vehicles for gene transfer in gene therapy of various human diseases.
Sajad Najafi   +6 more
doaj   +2 more sources

Lentiviral transduction of neuronal cells. [PDF]

open access: yesMethods Mol Biol, 2013
Here we describe a general method for the construction of a lentivirus vector using a specific example of the construction of a lentivirus containing the luciferase reporter gene under the control of two hypothetical promoters and derived HIV-1 based lentivirus expression vector pLVX-Puro.
Wollebo HS, Woldemichaele B, White MK.
europepmc   +4 more sources

Toward Tightly Tuned Gene Expression Following Lentiviral Vector Transduction [PDF]

open access: goldViruses, 2020
Lentiviral vectors are versatile tools for gene delivery purposes. While in the earlier versions of retroviral vectors, transgene expression was controlled by the long terminal repeats (LTRs), the latter generations of vectors, including those derived ...
Audrey Page   +2 more
doaj   +2 more sources

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