Christensen C B, Theander T G
Centre for Medical Parasitology, University of Copenhagen, Denmark.
J Immunoassay. 1997 May;18(2):129-48. doi: 10.1080/01971529708005809.
Using Tetanus Toxoid (TT) as a model antigen the T-cell Blotting method was evaluated. Peripheral blood mononuclear cell (PBMC) cultures were stimulated by blotted nitrocellulose-bound TT or soluble TT. SDS-Poly-Acrylamide-Gel-Electrophoresis separated TT only induced proliferation in 20% of the PBMC cultures whereas proliferation was induced in 79% of the same cultures offered similar treated TT (except for the PAGE separation). When T-cell blotting was performed with TT separated in a SDS-agarose matrix, proliferation was induced in 80% of donors responding to soluble TT. The results show that SDS-PAGE alters the ability of TT to induce T-cell proliferation, possibly due to unpolymerized acrylamide binding to proteins during SDS-PAGE. The use of SDS-PAGE T-cell blotting in the screening for T-cell antigens must therefore be reconsidered. We suggest the use of SDS-Agarose Gel Electrophoresis as an alternative when doing T-cell blots.
以破伤风类毒素(TT)作为模型抗原,对T细胞印迹法进行了评估。外周血单个核细胞(PBMC)培养物分别用印迹在硝酸纤维素膜上的TT或可溶性TT刺激。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分离的TT仅在20%的PBMC培养物中诱导增殖,而用经过类似处理的TT(除了PAGE分离)刺激相同的培养物时,79%的培养物出现增殖。当用在SDS-琼脂糖基质中分离的TT进行T细胞印迹时,80%对可溶性TT有反应的供体出现增殖。结果表明,SDS-PAGE改变了TT诱导T细胞增殖的能力,这可能是由于在SDS-PAGE过程中未聚合的丙烯酰胺与蛋白质结合所致。因此,在筛选T细胞抗原时,必须重新考虑使用SDS-PAGE T细胞印迹法。我们建议在进行T细胞印迹时,使用SDS-琼脂糖凝胶电泳作为替代方法。