Wedlock D N, Goh L P, McCarthy A R, Midwinter R G, Parlane N A, Buddle B M
AgResearch, Wallaceville Animal Research Centre, Upper Hutt, New Zealand.
Immunol Cell Biol. 1999 Feb;77(1):28-33. doi: 10.1046/j.1440-1711.1999.00793.x.
The present paper describes the physiological properties of recombinant possum TNF-alpha and an adjuvant effect on antibody responses to the model protein antigen, keyhole limpet haemocyanin (KLH). For these studies recombinant possum TNF-alpha was produced in the yeast Pichia pastoris. The recombinant cytokine was secreted into the culture medium and purified by gel filtration. Possum TNF-alpha produced in this expression system was N-glycosylated and bioactive in two different assays. In a murine fibroblast L929 cytotoxicity assay, the possum TNF-alpha had lower specific activity compared to human TNF-alpha, while in a possum-specific assay, possum TNF-alpha enhanced the proliferation of PHA-stimulated possum thymocytes and was more active than human TNF-alpha. The physiological effect of the recombinant possum TNF-alpha was investigated in groups of possums administered doses of 6, 30 or 150 micrograms of cytokine. For each dose, TNF-alpha caused profound effects on the numbers of circulating leucocytes characterized by a three-to-four-fold increase in neutrophil numbers at 6-24 h after injection and an initial sharp decrease in lymphocyte numbers. The efficacy of TNF-alpha as an immunological adjuvant was determined in possums administered KLH (125 micrograms) in an aqueous or Al(OH)3-based formulation with or without added recombinant TNF-alpha (150 micrograms). Serum antibody responses to KLH were monitored by ELISA. The TNF-alpha stimulated two-fold and four-fold increases in antibody levels in aqueous and Al(OH)3-based vaccine formulations, respectively. The strongest antibody responses were observed in the group of possums that received KLH formulated in Al(OH)3 with addition of TNF-alpha.
本文描述了重组负鼠肿瘤坏死因子-α(TNF-α)的生理特性及其对模型蛋白抗原——钥孔戚血蓝蛋白(KLH)抗体反应的佐剂效应。在这些研究中,重组负鼠TNF-α在毕赤酵母中产生。重组细胞因子分泌到培养基中并通过凝胶过滤进行纯化。在该表达系统中产生的负鼠TNF-α进行了N-糖基化修饰并且在两种不同的测定中具有生物活性。在小鼠成纤维细胞L929细胞毒性测定中,与人类TNF-α相比,负鼠TNF-α具有较低的比活性,而在负鼠特异性测定中,负鼠TNF-α增强了PHA刺激的负鼠胸腺细胞的增殖,并且比人类TNF-α更具活性。对给予6、30或150微克细胞因子剂量的负鼠组研究了重组负鼠TNF-α的生理效应。对于每个剂量,TNF-α对循环白细胞数量产生了深远影响,其特征是注射后6-24小时中性粒细胞数量增加三到四倍以及淋巴细胞数量最初急剧下降。在给予KLH(125微克)的负鼠中,以水性或基于氢氧化铝的制剂形式,添加或不添加重组TNF-α(150微克),测定TNF-α作为免疫佐剂的功效。通过ELISA监测对KLH的血清抗体反应。TNF-α分别在水性和基于氢氧化铝的疫苗制剂中刺激抗体水平增加两倍和四倍。在接受添加了TNF-α的氢氧化铝制剂形式的KLH的负鼠组中观察到最强的抗体反应。