Schaper W, Ito W D
Max-Planck-Institute for Physiological and Clinical Research, Department of Experimental Cardiology, Benekestrasse 2, D-61231 Bad Nauheim, Germany.
Curr Opin Biotechnol. 1996 Dec;7(6):635-40. doi: 10.1016/s0958-1669(96)80075-9.
The feasibility of gene therapy for cardiovascular diseases related to atherosclerosis is a topic that needs to be addressed. Most recent papers have dealt with technical aspects and feasibility and most of the genes transferred were reporter genes like those for beta-galactosidase or luciferase. This may mean that the ideal vector, one that is not pathogenic or immunotolerant but is still efficient, is still not available. The results of these studies are ambiguous and it has been doubted whether the genes targeted really affect the disease. Further efforts are therefore needed to elucidate the underlying pathophysiology.
基因治疗用于与动脉粥样硬化相关的心血管疾病的可行性是一个需要探讨的话题。最近的论文大多涉及技术方面和可行性,所转移的大多数基因都是报告基因,如β-半乳糖苷酶或荧光素酶的基因。这可能意味着理想的载体,即一种无致病性或具有免疫耐受性但仍高效的载体,仍然不可得。这些研究的结果不明确,人们怀疑所靶向的基因是否真的对疾病有影响。因此,需要进一步努力阐明潜在的病理生理学。