Ishikawa M, Yoshioka K, Urano K, Tanaka Y, Hatanaka T, Nii A
Central Research Laboratories, Research & Development Division, Seikagaku Corporation, Higashiyamato-shi, Tokyo, Japan.
Central Research Laboratories, Research & Development Division, Seikagaku Corporation, Higashiyamato-shi, Tokyo, Japan.
Osteoarthritis Cartilage. 2014 Nov;22(11):1902-9. doi: 10.1016/j.joca.2014.08.002. Epub 2014 Aug 19.
To compare the biocompatibility and immunogenicity of two intra-articular hyaluronan formulations, Gel-200 (Gel-One(®)) and hylan G-F 20 (Synvisc(®) series).
A comparison of the biocompatibility of Gel-200 and hylan G-F 20 was made using a rat subcutaneous air pouch model and the knee joint of normal rabbits. Immunogenicity was evaluated using a homologous passive cutaneous anaphylaxis (PCA) assay in guinea pigs.
In the air pouch model in rats, characteristic fibrous belts formed in the subcutaneous tissue. Injection of hylan G-F 20 into the air pouch induced granulomatous nodules primarily composed of macrophages, multinucleated giant cells, and eosinophils accompanied with the test material in the center of the nodules in the fibrous belt. Furthermore, the thickness of the fibrous belt in the hylan G-F 20 group increased significantly compared to the saline group. Injection of Gel-200 into the air pouch induced neither granulomatous inflammation nor significant thickening of fibrous belt, while foamy macrophages containing the test material were observed. Intra-articular injection of hylan G-F 20 into the rabbit knee joints induced granulomatous inflammation, eosinophil infiltration, and significant increase in the number of cells in the synovial fluid, while these findings were absent in the Gel-200 group. In the immunogenicity assay, hylan G-F 20 induced a positive PCA reaction, but the Gel-200 did not.
Gel-200 showed more favorable biocompatibility and less immunogenicity compared to hylan G-F 20. Gel-200 is expected to be a single injection hyaluronan product with less safety concerns for the treatment of knee osteoarthritis (OA) pain.
比较两种关节内透明质酸制剂Gel-200(Gel-One(®))和交联透明质酸钠凝胶(hylan G-F 20,Synvisc(®)系列)的生物相容性和免疫原性。
使用大鼠皮下气囊模型和正常兔膝关节比较Gel-200和交联透明质酸钠凝胶的生物相容性。在豚鼠中采用同源被动皮肤过敏反应(PCA)试验评估免疫原性。
在大鼠皮下气囊模型中,皮下组织形成特征性纤维带。向气囊内注射交联透明质酸钠凝胶诱导形成肉芽肿性结节,主要由巨噬细胞、多核巨细胞和嗜酸性粒细胞组成,结节中心伴有试验材料,位于纤维带内。此外,与生理盐水组相比,交联透明质酸钠凝胶组的纤维带厚度显著增加。向气囊内注射Gel-200既未诱导肉芽肿性炎症,纤维带也未显著增厚,但可见含有试验材料的泡沫巨噬细胞。向兔膝关节内注射交联透明质酸钠凝胶诱导肉芽肿性炎症、嗜酸性粒细胞浸润,滑液中细胞数量显著增加,而Gel-200组未出现这些表现。在免疫原性试验中,交联透明质酸钠凝胶诱导了阳性PCA反应,但Gel-200未诱导。
与交联透明质酸钠凝胶相比,Gel-200表现出更良好的生物相容性和更低的免疫原性。Gel-200有望成为一种单次注射的透明质酸产品,用于治疗膝关节骨关节炎(OA)疼痛时安全性担忧较少。