Modification of T-cell antigenic properties of tetanus toxoid by SDS-PAGE separation. Implications for T-cell blotting.

C B Christensen, T G Theander
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Abstract

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.

SDS-PAGE分离修饰破伤风类毒素t细胞抗原性。对t细胞印迹的影响。
以破伤风类毒素(Tetanus Toxoid, TT)为模型抗原,对t细胞印迹法进行了评价。外周血单个核细胞(PBMC)培养用印迹的硝化纤维素结合TT或可溶性TT刺激。sds -聚丙烯酰胺-凝胶电泳分离的TT仅在20%的PBMC培养物中诱导增殖,而在提供类似处理的TT的相同培养物中,有79%的培养物诱导增殖(PAGE分离除外)。将TT分离在sds -琼脂糖基质中进行t细胞印迹时,80%的供体对可溶性TT有反应,可诱导增殖。结果表明,SDS-PAGE改变了TT诱导t细胞增殖的能力,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。因此,必须重新考虑使用SDS-PAGE t细胞印迹技术筛选t细胞抗原。我们建议使用sds -琼脂糖凝胶电泳作为t细胞印迹的替代方法。
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