Hai Bo, Yan Xing, Voutetakis Antonis, Zheng Changyu, Cotrim Ana P, Shan Zhaochen, Ding Gang, Zhang Chunmei, Xu Junji, Goldsmith Corinne M, Afione Sandra, Chiorini John A, Baum Bruce J, Wang Songlin
Salivary Gland Disease Center and the Molecular Laboratory for Gene Therapy, School of Stomatology, Capital Medical University, Beijing, China.
J Gene Med. 2009 Jun;11(6):506-14. doi: 10.1002/jgm.1319.
Previously, using an adenoviral vector, we showed that miniature pigs could provide a valuable and affordable large animal model for pre-clinical gene therapy studies to correct parotid gland radiation damage. However, adenoviral vectors lead to short-term transgene expression and, ideally, a more stable correction is required. In the present study, we examined the suitability of using a serotype 2 adeno-associated viral (AAV2) vector to mediate more stable gene transfer in the parotid glands of these animals.
Heparan sulfate proteoglycan was detected by immunohistochemistry. beta-galactosidase expression was determined histochemically. An AAV2 vector encoding human erythropoietin (hEpo) was administered via Stensen's duct. Salivary and serum hEpo levels were measured using an enzyme-linked immunosorbent assay. Serum chemistry and hematological analyses were performed and serum antibodies to hEpo were measured throughout the study. Vector distribution was determined by a quantitative polymerase chain reaction.
Transgene expression was vector dose-dependent, with high levels of hEpo being detected for up to 32 weeks (i.e. the longest time studied). hEpo reached maximal levels during weeks 4-8, but declined to approximately 25% of these values by week 32. Haematocrits were elevated from week 2. Transduced animals exhibited low serum anti-hEpo antibodies (1 : 8-1 : 16). Vector biodistribution at animal sacrifice revealed that most copies were in the targeted parotid gland, with few being detected elsewhere. No consistent adverse changes in serum chemistry or hematology parameters were seen.
AAV2 vectors mediate extended gene transfer to miniature pig parotid glands and should be useful for testing pre-clinical gene therapy strategies aiming to correct salivary gland radiation damage.
此前,我们利用腺病毒载体证明,小型猪可为临床前基因治疗研究提供一种有价值且经济实惠的大型动物模型,用于纠正腮腺辐射损伤。然而,腺病毒载体导致转基因表达时间较短,理想情况下,需要更稳定的纠正方法。在本研究中,我们检测了使用2型腺相关病毒(AAV2)载体在这些动物腮腺中介导更稳定基因转移的适用性。
通过免疫组织化学检测硫酸乙酰肝素蛋白聚糖。通过组织化学测定β-半乳糖苷酶表达。编码人促红细胞生成素(hEpo)的AAV2载体通过斯滕森氏管给药。使用酶联免疫吸附测定法测量唾液和血清中的hEpo水平。在整个研究过程中进行血清化学和血液学分析,并测量血清中针对hEpo的抗体。通过定量聚合酶链反应确定载体分布。
转基因表达呈载体剂量依赖性,在长达32周(即研究的最长时间)内检测到高水平的hEpo。hEpo在第4至8周达到最高水平,但到第32周降至这些值的约25%。血细胞比容从第2周开始升高。转导的动物表现出低血清抗hEpo抗体(1:8 - 1:16)。动物处死后的载体生物分布显示,大多数拷贝位于靶向腮腺,在其他地方很少检测到。未观察到血清化学或血液学参数的一致不良变化。
AAV2载体介导向小型猪腮腺的延长基因转移,应有助于测试旨在纠正唾液腺辐射损伤的临床前基因治疗策略。