Cramer D V, Gill T J
Lab Invest. 1986 Aug;55(2):126-37.
Our understanding of the complex cellular interactions responsible for mediating effective immune responses has increased substantially in recent years. It is now clear that the genetic loci that control the interaction of the cells of the immune response encode groups of closely related cell-surface molecules. These molecules are the class I and class II antigens of the MHC, the differentiation antigens on lymphocyte subpopulations, and the receptors of various types, including the membrane immunoglobulin of B lymphocytes and the antigen receptors of T lymphocytes. Biochemical analysis of these cell surface molecules has demonstrated that they display important DNA sequence homologies. A polypeptide of approximately 110 amino acids comprises the basic building block for many of the cell surface molecules. Gradually, as a consequence of evolutionary development, the immune system has expanded its ability to respond to the external environment by an increased complexity of lymphocyte subpopulations and the surface structures that modulate their interaction. These cell surface molecules provide the structures that allow collaborative interaction of different cell types and that form the multiprotein receptor complexes involved in the recognition of, and specific response to, foreign antigens. Our future understanding of the control of the immune response will depend upon establishing the biochemical nature and the multifaceted interactions of these important molecules.
近年来,我们对介导有效免疫反应的复杂细胞间相互作用的理解有了显著提高。现在很清楚,控制免疫反应细胞相互作用的基因位点编码了一组密切相关的细胞表面分子。这些分子包括主要组织相容性复合体(MHC)的I类和II类抗原、淋巴细胞亚群上的分化抗原以及各种类型的受体,包括B淋巴细胞的膜免疫球蛋白和T淋巴细胞的抗原受体。对这些细胞表面分子的生化分析表明,它们具有重要的DNA序列同源性。大约由110个氨基酸组成的多肽构成了许多细胞表面分子的基本结构单元。随着进化发展,免疫系统逐渐通过增加淋巴细胞亚群的复杂性以及调节其相互作用的表面结构,扩大了对外部环境的反应能力。这些细胞表面分子提供了允许不同细胞类型协同相互作用的结构,并形成了参与识别外来抗原和对其产生特异性反应的多蛋白受体复合物。我们未来对免疫反应控制的理解将取决于确定这些重要分子的生化性质及其多方面的相互作用。