Chan P L, Sinclair N R
Immunology. 1971 Dec;21(6):967-81.
Pepsin digested, F(ab') antibody has less ability to inhibit an antibody response than has intact IgG antibody, when the antibodies were given one day after antigen. F(ab') antibody has to be given with antigen to attain maximal suppression, while IgG antibody, administered after antigen, is still highly immunosuppressive. The IgG antibody was able to terminate established immune responses, whereas F(ab') antibody could not do so. We interpret these findings to indicate that F(ab') antibody suppresses immune responses by simple masking of antigen, whereas IgG antibody alters the immune response through a further activity which takes place after antibody has combined with antigen. This further activity involves the Fc portion of antibody. Two alterations in immune mechanism are suggested: (1) increased destruction of antigen and (2) inactivation of the antibody forming cell precursor population by antigen—antibody complexes. This latter possibility is considered in detail. The tripartite inactivation model has been constructed to explain the presently known observations concerning immunosuppression by antibody and to make a prediction which has been verified. A further prediction concerning the affinities of antibodies produced under IgG or F(ab') antibody-mediated immunosuppression is put forward. Thymus-bone marrow cell synergism does not give a simple thymus cell dose-response relationship but a multi-phasic relationship where the response increases once the dose of thymus cells is decreased to a sufficiently low level. Such a dose-response relationship is not explainable in terms of the usual mechanisms proposed for thymus-bone marrow cell interaction and this deviation from a simple dose-response relationship is interpreted in terms of the proposed function of thymus-derived cells in controlling antibody feedback regulation.
当抗原注射一天后给予抗体时,胃蛋白酶消化的F(ab')抗体抑制抗体反应的能力比完整的IgG抗体弱。F(ab')抗体必须与抗原同时给予才能达到最大抑制效果,而在抗原之后给予的IgG抗体仍具有高度免疫抑制作用。IgG抗体能够终止已建立的免疫反应,而F(ab')抗体则不能。我们对这些发现的解释是,F(ab')抗体通过简单地掩盖抗原抑制免疫反应,而IgG抗体则通过抗体与抗原结合后发生的进一步活性改变免疫反应。这种进一步的活性涉及抗体的Fc部分。提出了免疫机制的两种改变:(1)抗原破坏增加;(2)抗原-抗体复合物使抗体形成细胞前体细胞群体失活。对后一种可能性进行了详细讨论。构建了三方失活模型来解释目前已知的关于抗体介导的免疫抑制的观察结果,并做出了一个已得到验证的预测。还提出了另一个关于在IgG或F(ab')抗体介导的免疫抑制下产生的抗体亲和力的预测。胸腺-骨髓细胞协同作用并不呈现简单的胸腺细胞剂量-反应关系,而是一种多相关系,即当胸腺细胞剂量降低到足够低的水平时反应会增强。这种剂量-反应关系无法用通常提出的胸腺-骨髓细胞相互作用机制来解释,这种偏离简单剂量-反应关系的情况根据胸腺来源细胞在控制抗体反馈调节中的拟议功能来解释。