Hildebrand K A, Deie M, Allen C R, Smith D W, Georgescu H I, Evans C H, Robbins P D, Woo S L
Musculoskeletal Research Center, Department of Orthopaedic Surgery, University of Pittsburgh, Pennsylvania 15213, USA.
J Orthop Res. 1999 Jan;17(1):37-42. doi: 10.1002/jor.1100170107.
Gene therapy is a technique that may offer advantages over current methods of cytokine delivery to ligaments. To determine if implanted genes could be expressed in normal and injured knee ligaments, the medial collateral ligament and anterior cruciate ligament were studied in 18 rabbits. A retroviral ex vivo technique using allograft medial collateral ligament and anterior cruciate ligament fibroblasts and an adenoviral in vivo technique were compared as methods for delivering the LacZ marker gene to knee ligaments. Bilateral knee surgeries were performed, and the rabbits were equally divided into three groups. Group 1 received the retrovirus and the medial collateral ligament was ruptured, Group 2 received the adenovirus and the medial collateral ligament was ruptured, and Group 3 received the adenovirus and the medial collateral ligament was not injured. The anterior cruciate ligament was not injured in any group. The medial collateral and anterior cruciate ligaments of the right knees received 10(6) allografted, transduced ligament fibroblasts or 10(9) adenovirus particles, whereas the ligaments of the left knee received a similar volume of saline solution only. Equal numbers of rabbits were killed at 10 days, 3 weeks, and 6 weeks following the procedure. Ligament samples were stained with X-gal to detect the expression of the LacZ gene product, beta-galactosidase. LacZ gene expression was evident in ruptured and uninjured medial collateral ligaments as well as in the anterior cruciate ligament. The expression lasted between 10 days and 3 weeks in the medial collateral and anterior cruciate ligaments with use of the retrovirus and between 3 and 6 weeks in the medial collateral ligament and at least 6 weeks in the anterior cruciate ligament with the adenovirus. The length of gene expression in the ruptured and uninjured medial collateral ligaments did not differ. These preliminary studies indicate that gene transfer to normal and injured knee ligaments is possible.
基因治疗是一种可能比目前向韧带递送细胞因子的方法更具优势的技术。为了确定植入的基因能否在正常和受伤的膝关节韧带中表达,对18只兔子的内侧副韧带和前交叉韧带进行了研究。比较了使用同种异体移植内侧副韧带和前交叉韧带成纤维细胞的逆转录病毒体外技术和腺病毒体内技术,作为将LacZ标记基因递送至膝关节韧带的方法。进行了双侧膝关节手术,并将兔子平均分为三组。第1组接受逆转录病毒,内侧副韧带破裂;第2组接受腺病毒,内侧副韧带破裂;第3组接受腺病毒,内侧副韧带未受伤。任何一组的前交叉韧带均未受伤。右膝的内侧副韧带和前交叉韧带接受10(6)个同种异体移植的、转导的韧带成纤维细胞或10(9)个腺病毒颗粒,而左膝的韧带仅接受相同体积的盐溶液。在手术后10天、3周和6周处死数量相等的兔子。用X-gal对韧带样本进行染色,以检测LacZ基因产物β-半乳糖苷酶的表达。LacZ基因表达在破裂和未受伤的内侧副韧带以及前交叉韧带中均很明显。使用逆转录病毒时,内侧副韧带和前交叉韧带中的表达持续10天至3周;使用腺病毒时,内侧副韧带中的表达持续3至6周,前交叉韧带中的表达至少持续6周。破裂和未受伤的内侧副韧带中基因表达的持续时间没有差异。这些初步研究表明,向正常和受伤的膝关节韧带进行基因转移是可能的。