Transduction of human CD34+ repopulating cells with a self-inactivating lentiviral vector for SCID-X1 produced at clinical scale by a stable cell line. (Q37066362)

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scientific article published on October 2012

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English	Transduction of human CD34+ repopulating cells with a self-inactivating lentiviral vector for SCID-X1 produced at clinical scale by a stable cell line.	scientific article published on October 2012

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scholarly article

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15 February 2020

Transduction of human CD34+ repopulating cells with a self-inactivating lentiviral vector for SCID-X1 produced at clinical scale by a stable cell line (English)

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15 February 2020

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15 February 2020

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15 February 2020

author name string

Michael R Greene

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15 February 2020

Timothy Lockey

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15 February 2020

Paul W Eldridge

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15 February 2020

John T Gray

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15 February 2020

Brian P Sorrentino

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publication date

1 October 2012

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15 February 2020

Human gene therapy methods

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15 February 2020

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15 February 2020

5

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15 February 2020

297-308

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15 February 2020

Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome

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29 September 2017

Gene therapy for primary adaptive immune deficiencies

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29 September 2017

The use of chromatin insulators to improve the expression and safety of integrating gene transfer vectors

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29 September 2017

Large-scale production means for the manufacturing of lentiviral vectors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732136

29 September 2017

Large-scale manufacture and characterization of a lentiviral vector produced for clinical ex vivo gene therapy application

1 reference

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29 September 2017

Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

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29 September 2017

Efficacy of gene therapy for X-linked severe combined immunodeficiency

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29 September 2017

Ex vivo expansion of retrovirally transduced primate CD34+ cells results in overrepresentation of clones with MDS1/EVI1 insertion sites in the myeloid lineage after transplantation.

1 reference

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29 September 2017

A self-inactivating lentiviral vector for SCID-X1 gene therapy that does not activate LMO2 expression in human T cells

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3732136

29 September 2017

Comparison of human cord blood engraftment between immunocompromised mouse strains

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29 September 2017

Transduction of human primitive repopulating hematopoietic cells with lentiviral vectors pseudotyped with various envelope proteins

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29 September 2017

Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

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29 September 2017

Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy

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29 September 2017

Comparison of human fetal liver, umbilical cord blood, and adult blood hematopoietic stem cell engraftment in NOD-scid/gammac-/-, Balb/c-Rag1-/-gammac-/-, and C.B-17-scid/bg immunodeficient mice

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29 September 2017

Sustained high-level polyclonal hematopoietic marking and transgene expression 4 years after autologous transplantation of rhesus macaques with SIV lentiviral vector-transduced CD34+ cells

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29 September 2017

The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy

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29 September 2017

Efficient construction of producer cell lines for a SIN lentiviral vector for SCID-X1 gene therapy by concatemeric array transfection

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29 September 2017

Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

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29 September 2017

Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

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29 September 2017

NOD/Shi-scid IL2rgamma(null) (NOG) mice more appropriate for humanized mouse models.

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29 September 2017

Physiological promoters reduce the genotoxic risk of integrating gene vectors

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29 September 2017

Inducible packaging cells for large-scale production of lentiviral vectors in serum-free suspension culture

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29 September 2017

An experimental system for the evaluation of retroviral vector design to diminish the risk for proto-oncogene activation

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29 September 2017

Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency

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29 September 2017

Suppression of clonal dominance in cultured human lymphoid cells by addition of the cHS4 insulator to a lentiviral vector

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29 September 2017

Unique risk factors for insertional mutagenesis in a mouse model of XSCID gene therapy

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29 September 2017

Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration

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29 September 2017

Development of functional human blood and immune systems in NOD/SCID/IL2 receptor {gamma} chain(null) mice

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29 September 2017

Generation of a packaging cell line for prolonged large-scale production of high-titer HIV-1-based lentiviral vector.

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29 September 2017

Distinct genomic integration of MLV and SIV vectors in primate hematopoietic stem and progenitor cells

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29 September 2017

Retroviral DNA integration: ASLV, HIV, and MLV show distinct target site preferences

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29 September 2017

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

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29 September 2017

Transcription start regions in the human genome are favored targets for MLV integration

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29 September 2017

HIV-1 integration in the human genome favors active genes and local hotspots

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29 September 2017

Generation of a stable cell line producing high-titer self-inactivating lentiviral vectors

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29 September 2017

A stable system for the high-titer production of multiply attenuated lentiviral vectors

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29 September 2017

Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery

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29 September 2017

Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice.

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29 September 2017

Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: implications for gene therapy

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29 September 2017

Lentiviral hematopoietic cell gene therapy for X-linked adrenoleukodystrophy

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4 September 2018

Long-term persistence of a polyclonal T cell repertoire after gene therapy for X-linked severe combined immunodeficiency

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4 September 2018

Optimal conditions for lentiviral transduction of engrafting human CD34+ cells

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4 September 2018

High-resolution insertion-site analysis by linear amplification-mediated PCR (LAM-PCR).

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4 September 2018

Clonal analysis of thymus-repopulating cells presents direct evidence for self-renewal division of human hematopoietic stem cells

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4 September 2018

Failure of SCID-X1 gene therapy in older patients

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4 September 2018

Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

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4 September 2018

Continuous high-titer HIV-1 vector production.

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4 September 2018

Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis

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4 September 2018

Primitive human hematopoietic cells are enriched in cord blood compared with adult bone marrow or mobilized peripheral blood as measured by the quantitative in vivo SCID-repopulating cell assay

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12 December 2020

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10.1089/HGTB.2012.150

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