Evidence map›Paper›PMID 25107584›Full record

ArticleStem cells translational medicine2014

Enhanced genetic modification of adult growth factor mobilized peripheral blood hematopoietic stem and progenitor cells with rapamycin.

Lijing Li, Mónica Torres-Coronado, Angel Gu, Anitha Rao, Agnes M Gardner, Elizabeth W Epps, Nancy Gonzalez, Chy-Anh Tran, Xiwei Wu, Jin-Hui Wang and 1 more

Abstract read
In one paragraph

Article in Stem cells translational medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Prostaglandin EMolecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Lijing LiShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Mónica Torres-CoronadoShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Angel GuShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Anitha RaoShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Agnes M GardnerShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Elizabeth W EppsShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Nancy GonzalezShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Chy-Anh TranShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Xiwei WuShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
Jin-Hui WangShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA.
David L DiGiustoShared Resources-Cellular Process, City of Hope, Duarte, California, USA; Center for Blood Cell Therapies at Peter McCallum Center, Melbourne, Australia; Departments of Molecular and Cellular Biology and Virology, City of Hope, Duarte, California, USA ddigiusto@coh.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic modification of adult human hematopoietic stem and progenitor cells (HSPCs) with lentiviral vectors leads to long-term gene expression in the progeny of the HSPCs and has been used to successfully treat several monogenic diseases. In some cases, the gene-modified cells have a selective growth advantage over nonmodified cells and eventually are the dominant engrafted population. However, in disease indications for which the gene-modified cells do not have a selective advantage, optimizing transduction of HSPC is paramount to successful stem cell-based gene therapy. We demonstrate here that transduction of adult CD34+ HSPCs with lentiviral vectors in the presence of rapamycin, a widely used mTORC1 inhibitor, results in an approximately threefold increase in stable gene marking with minimal effects on HSPC growth and differentiation. Using this approach, we have demonstrated that we can enhance the frequency of gene-modified HSPCs that give rise to clonogenic progeny in vitro without excessive increases in the number of vector copies per cell or changes in integration pattern. The genetic marking of HSPCs and expression of transgenes is durable, and transplantation of gene-modified HSPCs into immunodeficient mice results in high levels of gene marking of the lymphoid and myeloid progeny in vivo. The prior safe clinical history of rapamycin in other applications supports the use of this compound to generate gene-modified autologous HSPCs for our HIV gene therapy clinical trials.

Indexed as

AnimalsCell Culture TechniquesFlow CytometryGenetic TherapyGenetic VectorsGranulocyte Colony-Stimulating FactorHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansIn Vitro TechniquesLentivirusMiceMice, Inbred NODPolymerase Chain ReactionSirolimusTransduction, GeneticGranulocyte Colony-Stimulating FactorSirolimusGeneticHematopoietic stem cellsHIVMiceSCIDSirolimusTransductionTransplantation

Identifiers

PMID25107584
PMCPMC4181393

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.