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Hematopoietic malignancies and gene therapy

机译:造血系统恶性肿瘤与基因治疗

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摘要

In the case of hematopoietic malignancies, direct approach of gene therapy [gene transfer to cancer cells in order to obtain direct therapeutic effects (cell damage)] is difficult, because malignant cells are distributed in the whole body. As for indirect approaches, immuno-gene-therapy is investigated: As a unique approach, suicide gene therapy is applied to donor lymphocyte infusion for relapsed leukemia after bone marrow transplantation. The purpose of gene therapy is to eliminate donor lymphocytes quickly when severe side effects (GVHD) appeared. HSV-TK gene is generally utilized as a suicide gene. Basic studies are conducted to determine whether anti-tumor-angiogenesis therapy is also effective for hematological malignancies. In addition, leukemia development in 2 patients with X-linked severe combined immunodeficiency who underwent hematopoietic stem cell gene therapy is currently a serious problem in the field of gene therapy. In both cases, LMO2 gene was activated through insertional mutagenesis which was caused by retroviral vectormediated gene transfer. This genetic event is considered to be a trigger of T-lymphocytic leukemia development. Further basic studies are needed in terms of safety for stem cell gene therapy.
机译:在造血系统恶性肿瘤的情况下,基因治疗的直接方法[为了获得直接的治疗效果(细胞损伤)而将基因转移到癌细胞中]是困难的,因为恶性细胞遍布全身。对于间接途径,研究了免疫基因疗法:作为一种独特的途径,自杀基因疗法被应用于骨髓移植后复发性白血病的供体淋巴细胞输注。基因治疗的目的是在出现严重副作用(GVHD)时迅速消除供体淋巴细胞。 HSV-TK基因通常用作自杀基因。进行基础研究以确定抗肿瘤血管生成疗法是否也对血液系统恶性肿瘤有效。另外,接受造血干细胞基因治疗的2例X连锁严重合并免疫缺陷患者的白血病发展目前是基因治疗领域的一个严重问题。在这两种情况下,LMO2基因都通过插入诱变激活,这是由逆转录病毒载体介导的基因转移引起的。这种遗传事件被认为是T淋巴细胞白血病发展的诱因。就干细胞基因治疗的安全性而言,需要进一步的基础研究。

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