Allardyce R A, Anderson N F, Vaerman J P, James K
Clin Exp Immunol. 1973 Feb;13(2):263-78.
The antigenic and immunosuppressive properties of normal and antilympho-cytic equine globulin subfractions were investigated in the rat model in an attempt to increase the efficacy of prolonged ALG therapy by limiting the immunogenic stimulus of `inactive' subfractions. Chromatographic separation of equine IgG components yielded an electro-phoretically slow gamma 2 fraction consisting of IgG2a and IgG2b and a more heterogeneous fast gamma 1 subfraction. Immunosuppression resulting from the administration of isolated subfractions was measured by the response to alum-BSA and skin allograft survival. Antigenicity was determined by a variety of immunological procedures. The immunosuppressive character of the ALG was confined to the gamma 2 fraction, however this fraction also proved antigenic in our system. The administration of normal equine IgG subfractions in combination with Freund's complete adjuvant resulted in the demonstration of antigenic differences between the fast and slow IgG components.
在大鼠模型中研究了正常马球蛋白和抗淋巴细胞马球蛋白亚组分的抗原性和免疫抑制特性,试图通过限制“非活性”亚组分的免疫原性刺激来提高延长抗淋巴细胞球蛋白(ALG)治疗的疗效。马IgG成分的色谱分离产生了一个由IgG2a和IgG2b组成的电泳缓慢的γ2组分和一个更不均一的快速γ1亚组分。通过对明矾-牛血清白蛋白(alum-BSA)的反应和皮肤同种异体移植存活来测量给予分离亚组分后产生的免疫抑制作用。通过多种免疫学方法确定抗原性。ALG的免疫抑制特性局限于γ2组分,然而在我们的系统中该组分也被证明具有抗原性。将正常马IgG亚组分与弗氏完全佐剂联合给药导致证明了快速和慢速IgG成分之间的抗原性差异。