Sachs D H, Dickler H B
Transplant Rev. 1975;23:159-75. doi: 10.1111/j.1600-065x.1975.tb00156.x.
An hypothetical model has been presented by which I region determined cell surface molecules (Ia antigens) mediate the collaboration between T cells and B cells leading to control of the humoral immune response. The model proposes an analogy between Ia antigens and the constant regions of Ig chains. The absolute requirements of this model are: a) On the B cell the Ia antigen is closely associated with the Fc receptor; b) On the T cell the Ia antigen is closely associated with the product of a linked variable region gene which functions as a specific T cell binding site; and c) The interaction between the T cell Ia molecule and its B cell counterpart leads to B cell activation. By the proposed interactive model no additional Ir gene products are required to explain current concepts of Ir gene function. The experimental evidence from our own laboratory and elsewhere upon which this model is based has been reviewed and a variety of consequences and predictions of the model have been examined. There are numerous aspects of the model which, because of a lack of hard data, are open to alternative explanations. The possible usefulness of this model should lie in its ability to suggest further experiments to elucidate the mechanism of B cell activation and control of the immune response.
现已提出一个假设模型,据此,I区决定的细胞表面分子(Ia抗原)介导T细胞与B细胞之间的协作,从而调控体液免疫反应。该模型提出了Ia抗原与Ig链恒定区之间的类比关系。此模型的绝对必要条件为:a)在B细胞上,Ia抗原与Fc受体紧密相连;b)在T细胞上,Ia抗原与一个连锁可变区基因的产物紧密相连,该产物作为特异性T细胞结合位点发挥作用;c)T细胞Ia分子与其B细胞对应物之间的相互作用导致B细胞活化。根据所提出的交互模型,无需额外的Ir基因产物来解释当前的Ir基因功能概念。已对该模型所基于的来自我们自己实验室及其他地方的实验证据进行了综述,并对该模型的各种结果和预测进行了研究。由于缺乏确凿数据,该模型有许多方面可供其他解释。此模型的可能用途应在于其能够提示进一步的实验,以阐明B细胞活化及免疫反应调控的机制。