Highly efficient targeted transduction of undifferentiated human hematopoietic cells by adenoviral vectors displaying fiber knobs of subgroup B

Human Gene Therapy

Volumn 12, Issue 16, 2001, Pages 1989-2005

  Knaan Shanzer S ^a   Van der Velde, I ^a   Havenga, M J E ^a   Lemckert, A A C ^a   De Vries, A A F ^a   Valerio, D ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CD33 ANTIGEN; CD34 ANTIGEN; CD71 ANTIGEN; GREEN FLUORESCENT PROTEIN; RECOMBINANT DNA; VIRUS VECTOR;

ADENOVIRUS; ANTIGEN EXPRESSION; ARTICLE; BONE MARROW; CELL SUBPOPULATION; CHIMERA; CONTROLLED STUDY; FLOW CYTOMETRY; GENE CASSETTE; GENE EXPRESSION; GENETIC TRANSDUCTION; GRANULOCYTE; HEMATOPOIETIC CELL; HUMAN; HUMAN CELL; IMMEDIATE EARLY GENE; MONOCYTE; MOUSE; NONHUMAN; NORMAL HUMAN; SEROTYPE; STEM CELL;

ADENOVIRIDAE; BASE SEQUENCE; DNA PRIMERS; GENETIC VECTORS; GREEN FLUORESCENT PROTEINS; HEMATOPOIETIC STEM CELLS; HUMANS; IMMUNOPHENOTYPING; LEUKEMIA, ERYTHROBLASTIC, ACUTE; LUMINESCENT PROTEINS; TRANSDUCTION, GENETIC; TUMOR CELLS, CULTURED;

ADENOVIRIDAE; COXSACKIEVIRUS; CYTOMEGALOVIRUS; MIRIDAE; SUBGROUP B;

EID: 0035199416     PISSN: 10430342     EISSN: None     Source Type: Journal    
DOI: 10.1089/104303401753204562     Document Type: Article

References (70)

1. + cells with a human immunodeficiency virus type 1-based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G
2. Hepatocytes from non-hepatic adult stem cells
3. Adenovirus type 37 uses sialic acid as a cellular receptor
4. v integrins
5. Isolation of putative progenitor endothelial cells for angiogenesis
6. Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice
7. Construction and characterization of new cloning vehicles. II. A multipurpose cloning system
8. + cells
9. Lipofectamine and related cationic lipids strongly improve adenoviral infection efficiency of primitive human hematopoietic cells
10. - human hematopoietic cells by HIV-1-based lentiviral vectors
11. Selective transgene expression for detection and elimination of contaminating carcinoma cells in hematopoietic stem cell sources
12. Adenoviruses from human immunodeficiency virus-infected individuals, including two strains that represent new candidate serotypes Ad50 and Ad51 of species B1 and D, respectively
13. New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication-competent adenoviruses
14. Efficient adenoviral vector transduction of human hematopoietic SCID-repopulating and long-term culture-initiating cells
15. Muscle regeneration by bone marrow-derived progenitors
16. Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences
17. High-efficiency gene transfer into ex vivo expanded human hematopoietic progenitors and precursor cells by adenovirus vectors
18. Cytosine deaminase adenoviral vector and 5-fluorocytosine selectively reduce breast cancer cells 1 million-fold when they contaminate hematopoietic cells: A potential purging method for autologous transplantation
19. Generation of a high-capacity hybrid vector: Packaging of recombinant adeno-associated virus replicative intermediates in adenovirus capsids overcomes the limited cloning capacity of adeno-associated virus vectors
20. Dystrophin expression in the mdx mouse restored by stem cell transplantation
21. 2 domain at the surface of human epithelial and B lymphoblastoid cells
22. Genetic manipulation of primitive leukemic and normal hematopoietic cells using a novel method of Ad-mediated gene transfer
23. A monoclonal antibody specific for the cellular receptor for the group B coxsackieviruses
24. Adenovirus interaction with distinct integrins mediates separate events in cell entry and gene delivery to hematopoietic cells
25. A single amino acid in the adenovirus type 37 fiber confers binding to human conjunctival cells
26. Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors
27. Establishment and characterization of a unique human cell line that proliferates dependently on GM-CSF, IL-3, or erythropoietin
28. Intrinsic potential of phenotypically defined human hemopoietic stem cells to self-renew in short-term in vitro cultures
29. Genetic targeting of adenoviral vectors
30. Purified hematopoietic stem cells can differentiate into hepatocytes in vivo
31. Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus
32. Integrating adenovirus-adeno-associated virus hybrid vectors devoid of all viral genes
33. Effect of changes in expression of the amphotropic retroviral receptor PiT-2 on transduction efficiency and viral titer: Implications for gene therapy
34. Adenoviral vector-mediated gene transfer to primitive human hematopoietic progenitor cells: Assessment of transduction and toxicity in long-term culture
35. Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection
36. Fiber swap between adenovirus subgroups B and C alters intracellular trafficking of adenovirus gene transfer vectors
37. + cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors
38. Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector
39. Adenovirus-mediated expression of the murine ecotropic receptor facilitates transduction of human hematopoietic cells with an ecotropic retroviral vector
40. Transduction of primitive human hematopoietic cells with recombinant adenovirus vectors
41. The level of mRNA encoding the amphotropic retrovirus receptor in mouse and human hematopoietic cells is low and correlates with the efficiency of retrovirus transduction
42. Identification of human and mouse hematopoietic stem cell populations expressing high levels of mRNA encoding retrovirus receptors
43. Bone marrow as a potential source of hepatic oval cells
44. Identification of human immunodeficiency virus type 2 (HIV-2) encapsidation determinant and transduction of human cells by HIV-2-based lentivirus vectors
45. Maturation and lineage-specific expression of the coxsackie and adenovirus receptor in hematopoietic cells
46. Site-specific integration mediated by a hybrid adenovirus/adeno-associated virus vector
47. Transduction of non-dividing cells using pseudotyped defective high-titer HIV type 1 particles
48. Integration of murine leukemia virus DNA depends on mitosis
49. Comparative analysis of adenovirus fiber-cell interaction: Adenovirus type 2 (Ad2) and Ad9 utilize the same cellular fiber receptor but use different binding strategies for attachment
50. The coxsackievirus-adenovirus receptor protein can function as a cellular attachment protein for adenovirus serotypes from subgroups A, C, D, E, and F
51. Expression and function of cell adhesion molecules on fetal liver, cord blood and bone marrow hematopoietic progenitors: Implications for anatomical localization and developmental stage specific regulation of hematopoiesis
52. Adeno-associated virus vectors and hematology
53. Adeno-associated virus (AAV) Rep protein enhances the generation of a recombinant mini-adenovirus (Ad) utilizing an Ad/AAV hybrid virus
54. + cells
55. Adenovirus types 11p and 35p show high binding efficiencies for committed hematopoietic cell lines and are infective to these cell lines
56. Analytical anion-exchange HPLC of recombinant type-5 adenoviral particles
57. + cells by a retargeted adenovirus vector
58. Potential molecular approach to ex vivo hematopoietic expansion with recombinant epidermal growth factor receptor-expressing adenovirus vector
59. Derivation of hepatocytes from bone marrow cells in mice after radiation-induced myeloablation
60. Liver from bone marrow in humans
61. + cell populations derived from human umbilical cord blood using flow cytometry and cDNA-polymerase chain reaction
62. 1 human hematopoietic stem cells
63. Site-specific integration of a transgene mediated by a hybrid adenovirus/adeno-associated virus vector using the Cre/loxP-expression-switch system
64. Adenovirus vector pseudotyping in fiber-expressing cell lines: Improved transduction of Epstein-Barr virus-transformed B cells
65. A chimeric type 2 adenovirus vector with a type 17 fiber enhances gene transfer to human airway epithelia
66. Genomic integration and gene expression by a modified adenoviral vector