Literature DB >> 7644487

High-efficiency retroviral-mediated gene transfer into human and nonhuman primate peripheral blood lymphocytes.

B A Bunnell1, L M Muul, R E Donahue, R M Blaese, R A Morgan.   

Abstract

Peripheral blood lymphocytes (PBLs) are primary targets for gene therapy of inherited and acquired disorders of the immune system. We describe the development of an optimized transduction system that provides for high-efficiency retrovirus-mediated gene transfer into primary PBLs. This optimized transduction protocol combines centrifugation of the lymphocytes (1000 x g) at the inception of transduction with phosphate depletion, low-temperature incubation (32 degrees C), and the use of the packaging cell line PG13. Gene marking studies of human and primate PBLs using these optimized transduction conditions demonstrated that the transduction efficiency exceeded 50% of the total lymphocyte population. The optimized transduction efficiency of PBLs with amphotropic retroviral vectors was in excess of 25%. The transduction procedure does not alter phenotype, viability, or expansion of the transduced cells. Our data indicate that this optimized transduction system leads to high-efficiency gene transfer into primary human lymphocytes, which obviates the requirement for selection of transduced cells prior to gene-therapy procedures. Thus, large quantities of healthy retrovirally transduced lymphocytes containing a broad immunological repertoire can be generated for use in clinical protocols. Our results represent a significant improvement in the methodology for the transduction of lymphocytes for gene therapy.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7644487      PMCID: PMC41221          DOI: 10.1073/pnas.92.17.7739

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  17 in total

1.  The ADA human gene therapy clinical protocol: Points to Consider response with clinical protocol, July 6, 1990.

Authors:  W French Anderson; R Michael Blaese; Kenneth Culver
Journal:  Hum Gene Ther       Date:  1990       Impact factor: 5.695

2.  Improved retroviral vectors for gene transfer and expression.

Authors:  A D Miller; G J Rosman
Journal:  Biotechniques       Date:  1989-10       Impact factor: 1.993

3.  Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production.

Authors:  A D Miller; C Buttimore
Journal:  Mol Cell Biol       Date:  1986-08       Impact factor: 4.272

4.  Human gene transfer: characterization of human tumor-infiltrating lymphocytes as vehicles for retroviral-mediated gene transfer in man.

Authors:  A Kasid; S Morecki; P Aebersold; K Cornetta; K Culver; S Freeman; E Director; M T Lotze; R M Blaese; W F Anderson
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

5.  Further evaluation of soluble CD4 as an anti-HIV type 1 gene therapy: demonstration of protection of primary human peripheral blood lymphocytes from infection by HIV type 1.

Authors:  R A Morgan; G Baler-Bitterlich; J A Ragheb; F Wong-Staal; R C Gallo; W F Anderson
Journal:  AIDS Res Hum Retroviruses       Date:  1994-11       Impact factor: 2.205

6.  Cell-surface receptors for gibbon ape leukemia virus and amphotropic murine retrovirus are inducible sodium-dependent phosphate symporters.

Authors:  M P Kavanaugh; D G Miller; W Zhang; W Law; S L Kozak; D Kabat; A D Miller
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-19       Impact factor: 11.205

7.  Expression of human adenosine deaminase from various strong promoters after gene transfer into human hematopoietic cell lines.

Authors:  R A Hock; A D Miller; W R Osborne
Journal:  Blood       Date:  1989-08-01       Impact factor: 22.113

8.  Recombinant adeno-associated virus-mediated gene transfer into hematopoietic progenitor cells.

Authors:  S Goodman; X Xiao; R E Donahue; A Moulton; J Miller; C Walsh; N S Young; R J Samulski; A W Nienhuis
Journal:  Blood       Date:  1994-09-01       Impact factor: 22.113

9.  Applications of the polymerase chain reaction in retroviral-mediated gene transfer and the analysis of gene-marked human TIL cells.

Authors:  R A Morgan; K Cornetta; W F Anderson
Journal:  Hum Gene Ther       Date:  1990       Impact factor: 5.695

10.  In vivo expression and survival of gene-modified T lymphocytes in rhesus monkeys.

Authors:  K W Culver; R A Morgan; W R Osborne; R T Lee; D Lenschow; C Able; K Cornetta; W F Anderson; R M Blaese
Journal:  Hum Gene Ther       Date:  1990       Impact factor: 5.695

View more
  43 in total

Review 1.  Gene delivery into primary T cells: overview and characterization of a transgenic model for efficient adenoviral transduction.

Authors:  Vincent Hurez; Robin D Hautton; James Oliver; R James Matthews; Casey K Weaver
Journal:  Immunol Res       Date:  2002       Impact factor: 2.829

2.  Human immunodeficiency virus type 1 spinoculation enhances infection through virus binding.

Authors:  U O'Doherty; W J Swiggard; M H Malim
Journal:  J Virol       Date:  2000-11       Impact factor: 5.103

Review 3.  Targeting antibodies to the cytoplasm.

Authors:  Andrea L J Marschall; André Frenzel; Thomas Schirrmann; Manuela Schüngel; Stefan Dübel
Journal:  MAbs       Date:  2011-01-01       Impact factor: 5.857

4.  In vivo gene transfer into adult stem cells in unconditioned mice by in situ delivery of a lentiviral vector.

Authors:  D Nicole Worsham; Todd Schuesler; Christof von Kalle; Dao Pan
Journal:  Mol Ther       Date:  2006-08-07       Impact factor: 11.454

5.  Efficient Transduction of Human and Rhesus Macaque Primary T Cells by a Modified Human Immunodeficiency Virus Type 1-Based Lentiviral Vector.

Authors:  Huan He; Jing Xue; Weiming Wang; Lihong Liu; Chaobaihui Ye; Zhe Cong; Jason T Kimata; Chuan Qin; Paul Zhou
Journal:  Hum Gene Ther       Date:  2016-12-29       Impact factor: 5.695

6.  Scaffold attachment region-mediated enhancement of retroviral vector expression in primary T cells.

Authors:  M Agarwal; T W Austin; F Morel; J Chen; E Böhnlein; I Plavec
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

7.  Efficient infection of a human T-cell line and of human primary peripheral blood leukocytes with a pseudotyped retrovirus vector.

Authors:  S Sharma; M Cantwell; T J Kipps; T Friedmann
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

8.  Apaf-1- and Caspase-8-independent apoptosis.

Authors:  T Imao; S Nagata
Journal:  Cell Death Differ       Date:  2012-11-30       Impact factor: 15.828

9.  EWS-FLI-1-targeted cytotoxic T-cell killing of multiple tumor types belonging to the Ewing sarcoma family of tumors.

Authors:  Christopher H Evans; Fangjun Liu; Ryan M Porter; Regina P O'Sullivan; Taha Merghoub; Elaine P Lunsford; Kyle Robichaud; Frans Van Valen; Stephen L Lessnick; Mark C Gebhardt; James W Wells
Journal:  Clin Cancer Res       Date:  2012-08-09       Impact factor: 12.531

10.  Influenza virus-specific TCR-transduced T cells as a model for adoptive immunotherapy.

Authors:  Belinda Berdien; Henrike Reinhard; Sabrina Meyer; Stefanie Spöck; Nicolaus Kröger; Djordje Atanackovic; Boris Fehse
Journal:  Hum Vaccin Immunother       Date:  2013-02-21       Impact factor: 3.452

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.