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IDIOTYPIC REGULATION OF B CELL DIFFERENTIATION

机译:B细胞分化的独特型调控

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We study the equilibrium properties of idiotypically interacting B cell clones in the case where only the differentiation of B cells is affected by idiotypic interactions. Furthermore, we assume that clones may recognize and be stimulated by self antigen in the same fashion as by anti-antibodies. For idiotypically interacting pairs of non-autoreactive clones we observe three qualitatively different dynamical regimes. In the first regime, at small antibody production an antibody-free fixed point, the virgin state, is the only attractor of the system. For intermediate antibody production, a symmetric activated state replaces the virgin state as the only attractor of the system. For large antibody production, finally, the symmetric activated state gives way to two asymmetric activated states where one clone suppresses the other clone. If one or both clones in the pair are autoreactive there is no virgin state. However, we still observe the switch from an almost symmetric activated state to two asymmetric activated states. The two asymmetric activated states at high antibody production have profoundly different implications for a self antigen which is recognized by one of the clones of the pair. In the attractor characterized by high autoantibody concentration the self antigen is attacked vigorously by the immune system while in the opposite steady state the tiny amount of autoantibody hardly affects the self antigen. Accordingly, we call the first state the autoimmune state and the second the tolerant state. In the tolerant state the autoreactive clone is down-regulated by its anti-idiotype providing an efficient mechanism to prevent an autoimmune reaction. However, the antibody production required to achieve this anti-idiotypic control of autoantibodies is rather large.
机译:我们研究了独特型相互作用的B细胞克隆的平衡特性,其中只有B细胞的分化受到独特型相互作用的影响。此外,我们假设克隆可能以与抗抗体相同的方式识别自身抗原并受到自身抗原的刺激。对于非自动反应性克隆的独特型相互作用对,我们观察到了三个定性不同的动力学机制。在第一种方案中,在少量抗体产生时,无抗体的固定点(原始状态)是系统的唯一吸引子。对于中间抗体的生产,对称激活状态取代了原始状态,成为系统的唯一吸引子。最后,为了产生大量抗体,对称激活状态被两个不对称激活状态所取代,其中一个克隆抑制了另一个克隆。如果一对中的一个或两个克隆是自动反应的,则没有原始状态。但是,我们仍然观察到从几乎对称的激活状态到两个非对称的激活状态的切换。高抗体产生时的两个不对称激活状态对自身抗原具有深远不同的意义,该自身抗原被该对克隆中的一个识别。在以高自身抗体浓度为特征的吸引子中,自身抗原受到免疫系统的强烈攻击,而在相反的稳定状态下,极少量的自身抗体几乎不会影响自身抗原。因此,我们称第一状态为自身免疫状态,第二状态为耐受状态。在耐受状态下,自身反应性克隆通过其抗独特型被下调,从而提供了一种防止自身免疫反应的有效机制。然而,实现自身抗体的这种抗独特型控制所需的抗体产量相当大。

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