Hermens W T, ter Brake O, Dijkhuizen P A, Sonnemans M A, Grimm D, Kleinschmidt J A, Verhaagen J
Graduate School for Neurosciences Amsterdam, Netherlands Institute for Brain Research.
Hum Gene Ther. 1999 Jul 20;10(11):1885-91. doi: 10.1089/10430349950017563.
Recombinant adeno-associated virus (rAAV) vectors have become attractive tools for in vivo gene transfer. The production and purification of high-titer rAAV vector stocks for experimental and therapeutic gene transfer continue to undergo improvement. Standard rAAV vector purification protocols include the purification of the vector by cesium chloride (CsCl)-density gradient centrifugation followed by extensive desalination via dialysis against a physiological buffer for in vivo use. These procedures are extremely time consuming and frequently result in a substantial loss of the infectious vector titer. As an alternative to CsCl we have investigated the use of Iodixanol, an X-ray contrast solution, as the density-gradient medium. Purification of rAAV vectors by Iodixanol shortened the centrifugation period to 3 hr and resulted in reproducible concentration and purification of rAAV-vector stocks. We show that injection of rAAV derived from an Iodixanol gradient can be used for in vivo gene transfer applications in the brain and spinal cord without detectable cytopathic effects and directing stable transgene expression for at least 2 months.
重组腺相关病毒(rAAV)载体已成为体内基因转移的有吸引力的工具。用于实验性和治疗性基因转移的高滴度rAAV载体储备的生产和纯化仍在不断改进。标准的rAAV载体纯化方案包括通过氯化铯(CsCl)密度梯度离心纯化载体,然后通过针对生理缓冲液进行透析进行广泛脱盐以供体内使用。这些程序极其耗时,并且经常导致感染性载体滴度大幅损失。作为CsCl的替代方法,我们研究了使用碘克沙醇(一种X射线造影剂)作为密度梯度介质。用碘克沙醇纯化rAAV载体将离心时间缩短至3小时,并实现了rAAV载体储备的可重复浓缩和纯化。我们表明,注射源自碘克沙醇梯度的rAAV可用于脑和脊髓的体内基因转移应用,且无明显细胞病变效应,并能指导稳定的转基因表达至少2个月。