Viruses | |
Retroviral Vectors: Post Entry Events and Genomic Alterations | |
Ali Nowrouzi1  Hanno Glimm1  Christof Von Kalle1  | |
[1] 1Department of Translational Oncology, German Cancer Research Center, Im Neuenheimer Feld 581, 69120 Heidelberg, Germany 2National Center for Tumor Diseases, Im Neuenheimer Feld 581, 69120 Heidelberg, Germany | |
关键词: retroviral vectors; retroviral integration; gene therapy; insertional mutagenesis; vector genotoxicity; Leukemia; common insertion sites; | |
DOI : 10.3390/v3050429 | |
来源: mdpi | |
【 摘 要 】
The curative potential of retroviral vectors for somatic gene therapy has been demonstrated impressively in several clinical trials leading to sustained long-term correction of the underlying genetic defect. Preclinical studies and clinical monitoring of gene modified hematopoietic stem and progenitor cells in patients have shown that biologically relevant vector induced side effects, ranging from in vitro immortalization to clonal dominance and oncogenesis in vivo, accompany therapeutic efficiency of integrating retroviral gene transfer systems. Most importantly, it has been demonstrated that the genotoxic potential is not identical among all retroviral vector systems designed for clinical application. Large scale viral integration site determination has uncovered significant differences in the target site selection of retrovirus subfamilies influencing the propensity for inducing genetic alterations in the host genome. In this review we will summarize recent insights gained on the mechanisms of insertional mutagenesis based on intrinsic target site selection of different retrovirus families. We will also discuss examples of side effects occurring in ongoing human gene therapy trials and future prospectives in the field.
【 授权许可】
CC BY
This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
【 预 览 】
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RO202003190049537ZK.pdf | 686KB | download |