In vivo retrovirus-mediated gene transfer into multiple hematopoietic lineages in rabbits without preconditioning

被引:19
|
作者
Nelson, DM
Metzger, ME
Donahue, RE
Morgan, RA
机构
[1] NIH,NATL CTR HUMAN GENOME RES,CLIN GENE THERAPY BRANCH,GENE TRANSFER TECHNOL SECT,BETHESDA,MD 20892
[2] NHLBI,NIH,BETHESDA,MD 20892
关键词
D O I
10.1089/hum.1997.8.6-747
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hematopoietic progenitor cells are attractive targets for gene therapy of inherited and acquired disorders, We have developed a novel procedure for mediating gene transfer into hematopoietic cells using an in vivo approach, The procedure involves injection of irradiated retroviral producer cells into the femoral bone marrow cavity in rabbits without preconditioning, The emergence of vector-marked cells in multiple peripheral blood hematopoietic lineages was detected 1 week post-injection and persisted until the animals were sacrificed up to 20 months later, Vector-marked cells were also detected in different hematopoietic tissues including bone marrow, spleen, thymus, and lymph node, Expression of retrovirus-specific messages by reverse transcription polymerase chain reaction was detected at multiple time points up to 20 months. Retrovirally encoded protein was detected by enzyme-linked immunosorbent assay in supernatant from cultures of granulocytes isolated 14 months after the procedure, This work demonstrates the feasibility of effecting gene transfer into hematopoietic progenitor cells in vivo.
引用
收藏
页码:747 / 754
页数:8
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