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Retroviral vectors: from cancer viruses to therapeutic tools.

作者信息

Miller A Dusty

机构信息

Fred Hutchinson Cancer Research Center , Seattle, WA 98109.

出版信息

Hum Gene Ther. 2014 Dec;25(12):989-94. doi: 10.1089/hum.2014.2542.

DOI:10.1089/hum.2014.2542
PMID:25458252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4270132/
Abstract
摘要

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本文引用的文献

1
Hematopoietic stem cell gene therapy: progress on the clinical front.造血干细胞基因治疗：临床前沿进展
Hum Gene Ther. 2014 Mar;25(3):165-70. doi: 10.1089/hum.2014.2504. Epub 2014 Feb 28.
2
Adoptive immunotherapy with genetically modified lymphocytes in allogeneic stem cell transplantation.异基因造血干细胞移植中基因修饰淋巴细胞的过继免疫治疗。
Immunol Rev. 2014 Jan;257(1):165-80. doi: 10.1111/imr.12130.
3
Xpr1 is an atypical G-protein-coupled receptor that mediates xenotropic and polytropic murine retrovirus neurotoxicity.Xpr1 是一种非典型的 G 蛋白偶联受体，可介导异嗜性和多嗜性鼠逆转录病毒的神经毒性。
J Virol. 2012 Feb;86(3):1661-9. doi: 10.1128/JVI.06073-11. Epub 2011 Nov 16.
4
Hematopoietic stem cell gene therapy for adenosine deaminase-deficient severe combined immunodeficiency leads to long-term immunological recovery and metabolic correction.腺苷脱氨酶缺乏症严重联合免疫缺陷症的造血干细胞基因治疗可实现长期免疫恢复和代谢纠正。
Sci Transl Med. 2011 Aug 24;3(97):97ra80. doi: 10.1126/scitranslmed.3002716.
5
Long-term persistence of a polyclonal T cell repertoire after gene therapy for X-linked severe combined immunodeficiency.基因治疗 X 连锁重症联合免疫缺陷后多克隆 T 细胞 repertoire 的长期持久性。
Sci Transl Med. 2011 Aug 24;3(97):97ra79. doi: 10.1126/scitranslmed.3002715.
6
Gene therapy for immunodeficiency due to adenosine deaminase deficiency.针对腺苷脱氨酶缺乏所致免疫缺陷的基因治疗。
N Engl J Med. 2009 Jan 29;360(5):447-58. doi: 10.1056/NEJMoa0805817.
7
Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients.插入诱变与获得性体细胞突变相结合导致了SCID-X1患者基因治疗后的白血病发生。
J Clin Invest. 2008 Sep;118(9):3143-50. doi: 10.1172/JCI35798.
8
Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1.4例X连锁重症联合免疫缺陷病（SCID-X1）患者在逆转录病毒介导的基因治疗后发生插入性致癌作用。
J Clin Invest. 2008 Sep;118(9):3132-42. doi: 10.1172/JCI35700.
9
Improved enzootic nasal tumor virus pseudotype packaging cell lines reveal virus entry requirements in addition to the primary receptor Hyal2.改良的地方性鼻肿瘤病毒假型包装细胞系揭示了除主要受体Hyal2之外的病毒进入需求。
J Virol. 2005 Jan;79(1):87-94. doi: 10.1128/JVI.79.1.87-94.2005.
10
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1.两名接受X连锁重症联合免疫缺陷（SCID-X1）基因治疗的患者中与LMO2相关的克隆性T细胞增殖。
Science. 2003 Oct 17;302(5644):415-9. doi: 10.1126/science.1088547.