Carneiro J, Coutinho A, Faro J, Stewart J
Unité d'Immubiologie, CNRS URA 1961, Institut Pasteur, Paris, France,
J Theor Biol. 1996 Oct 21;182(4):513-29. doi: 10.1006/jtbi.1996.0192.
Hitherto, "second generation" network models of the immune system have all been restricted to B-lymphocytes and the Ig molecules they produce. These models have not so far been able to provide a convincing mechanism for the distinction between a "Central Immune System" (CIS) composed of a connected network of lymphocyte clones which couple with "self" antigens in a tolerant mode, and a "Peripheral Immune System" (PIS) composed of clones with little or no supra-clonal organization and which produce classical immune responses when interacting with "non-self" antigens. Here, we present a new network model which explicitly incorporates B-T cell co-operation. In this model, B-cell activation is dependent on T-cell help, and activated T-cells are down-regulated by engagement of their TCRs by soluble Ig. We discuss the underlying biology on which we base the system of ordinary differential equations which defines the present network model. We then illustrate some basic features of the model by examining several prototypical situations with a small number of clones. Depending on the idiotypic connectivity structure, the model exhibits two distinct modes of coupling with antigens: an "immune response" mode in which T- and B-cell clones grow exponentially; and a "tolerant" mode in which T-cell clones are controlled by inclusion of all TCRs in the repertoire of an idiotypic B-cell network. Finally, we discuss the simplifying assumptions of the present model and argue that its range of validity is indeed the region of the state-space of the system where the discrimination between the CIS and the PIS take place.
迄今为止,免疫系统的“第二代”网络模型都局限于B淋巴细胞及其产生的免疫球蛋白分子。到目前为止,这些模型还无法提供一个令人信服的机制,来区分由以耐受模式与“自身”抗原结合的淋巴细胞克隆连接网络组成的“中枢免疫系统”(CIS)和由几乎没有或没有超克隆组织、与“非自身”抗原相互作用时产生经典免疫反应的克隆组成的“外周免疫系统”(PIS)。在此,我们提出一种新的网络模型,该模型明确纳入了B细胞与T细胞的合作。在这个模型中,B细胞的激活依赖于T细胞的辅助,而活化的T细胞通过可溶性免疫球蛋白与它们T细胞受体的结合而被下调。我们讨论了定义当前网络模型的常微分方程组所基于的基础生物学原理。然后,我们通过研究少数克隆的几种典型情况来说明该模型的一些基本特征。根据独特型连接结构,该模型表现出与抗原耦合的两种不同模式:一种是“免疫反应”模式,其中T细胞和B细胞克隆呈指数增长;另一种是“耐受”模式,其中T细胞克隆通过将所有T细胞受体纳入独特型B细胞网络的库中而受到控制。最后,我们讨论了当前模型的简化假设,并认为其有效性范围确实是系统状态空间中区分CIS和PIS的区域。