Yamada Koichiro, Tsukahara Tomonori, Yoshino Kazuhisa, Kojima Katsuhiko, Agawa Hideyuki, Yamashita Yuki, Amano Yuji, Hatta Mariko, Matsuzaki Yasunori, Kurotori Naoki, Wakui Keiko, Fukushima Yoshimitsu, Osada Ryosuke, Shiozawa Tanri, Sakashita Kazuo, Koike Kenichi, Kumaki Satoru, Tanaka Nobuyuki, Takeshita Toshikazu
Department of Microbiology and Immunology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano, 390-8621, Japan.
Retrovirology. 2009 Sep 2;6:79. doi: 10.1186/1742-4690-6-79.
Therapeutic retroviral vector integration near the oncogene LMO2 is thought to be a cause of leukemia in X-SCID gene therapy trials. However, no published studies have evaluated the frequency of vector integrations near exon 1 of the LMO2 locus. We identified a high incidence region (HIR) of vector integration using PCR techniques in the upstream region close to the LMO2 transcription start site in the TPA-Mat T cell line. The integration frequency of the HIR was one per 4.46 x 10(4) cells. This HIR was also found in Jurkat T cells but was absent from HeLa cells. Furthermore, using human cord blood-derived CD34+ cells we identified a HIR in a similar region as the TPA-Mat T cell line. One of the X-linked severe combined immunodeficiency (X-SCID) patients that developed leukemia after gene therapy had a vector integration site in this HIR. Therefore, the descriptions of the location and the integration frequency of the HIR presented here may help us to better understand vector-induced leukemogenesis.
在X连锁重症联合免疫缺陷病(X-SCID)基因治疗试验中,治疗性逆转录病毒载体整合在致癌基因LMO2附近被认为是白血病发生的一个原因。然而,尚无已发表的研究评估LMO2基因座外显子1附近载体整合的频率。我们利用PCR技术在TPA-Mat T细胞系中靠近LMO2转录起始位点的上游区域鉴定出一个载体整合高发区(HIR)。该HIR的整合频率为每4.46×10⁴个细胞中有1个。在Jurkat T细胞中也发现了这个HIR,但HeLa细胞中没有。此外,利用人脐带血来源的CD34⁺细胞,我们在与TPA-Mat T细胞系相似的区域鉴定出一个HIR。基因治疗后发生白血病的一名X连锁重症联合免疫缺陷病(X-SCID)患者在这个HIR中有一个载体整合位点。因此,本文所呈现的HIR的位置和整合频率描述可能有助于我们更好地理解载体诱导的白血病发生机制。