Skakauskas Vladas, Katauskis Pranas, Skvortsov Alex
Vilnius University, 24 Naugarduko st, LT-03225, Vilnius, Lithuania.
Theor Biol Med Model. 2011 Sep 7;8:32. doi: 10.1186/1742-4682-8-32.
It was recently shown that the treatment effect of an antibody can be described by a consolidated parameter which includes the reaction rates of the receptor-toxin-antibody kinetics and the relative concentration of reacting species. As a result, any given value of this parameter determines an associated range of antibody kinetic properties and its relative concentration in order to achieve a desirable therapeutic effect. In the current study we generalize the existing kinetic model by explicitly taking into account the diffusion fluxes of the species.
A refined model of receptor-toxin-antibody (RTA) interaction is studied numerically. The protective properties of an antibody against a given toxin are evaluated for a spherical cell placed into a toxin-antibody solution. The selection of parameters for numerical simulation approximately corresponds to the practically relevant values reported in the literature with the significant ranges in variation to allow demonstration of different regimes of intracellular transport.
The proposed refinement of the RTA model may become important for the consistent evaluation of protective potential of an antibody and for the estimation of the time period during which the application of this antibody becomes the most effective. It can be a useful tool for in vitro selection of potential protective antibodies for progression to in vivo evaluation.
最近研究表明,抗体的治疗效果可用一个综合参数来描述,该参数包括受体 - 毒素 - 抗体动力学的反应速率以及反应物种的相对浓度。因此,该参数的任何给定值都决定了抗体动力学特性及其相对浓度的相关范围,以实现理想的治疗效果。在本研究中,我们通过明确考虑物种的扩散通量对现有动力学模型进行了推广。
对受体 - 毒素 - 抗体(RTA)相互作用的改进模型进行了数值研究。针对置于毒素 - 抗体溶液中的球形细胞,评估了抗体对给定毒素的保护特性。数值模拟参数的选择大致对应于文献中报道的实际相关值,且具有显著的变化范围,以便展示细胞内运输的不同机制。
所提出的RTA模型改进对于一致评估抗体的保护潜力以及估计该抗体应用最有效的时间段可能变得很重要。它可以成为体外筛选潜在保护性抗体以推进体内评估的有用工具。