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抗体依赖的细胞介导的细胞毒性(ADCC)的数学模型。

A mathematical model of antibody-dependent cellular cytotoxicity (ADCC).

作者信息

Hoffman F, Gavaghan D, Osborne J, Barrett I P, You T, Ghadially H, Sainson R, Wilkinson R W, Byrne H M

机构信息

Department of Computer Science, University of Oxford, Oxford, UK.

Department of Computer Science, University of Oxford, Oxford, UK; School of Mathematics and Statistics, University of Melbourne, AUS.

出版信息

J Theor Biol. 2018 Jan 7;436:39-50. doi: 10.1016/j.jtbi.2017.09.031. Epub 2017 Sep 29.

Abstract

Immunotherapies exploit the immune system to target and kill cancer cells, while sparing healthy tissue. Antibody therapies, an important class of immunotherapies, involve the binding to specific antigens on the surface of the tumour cells of antibodies that activate natural killer (NK) cells to kill the tumour cells. Preclinical assessment of molecules that may cause antibody-dependent cellular cytotoxicity (ADCC) involves co-culturing cancer cells, NK cells and antibody in vitro for several hours and measuring subsequent levels of tumour cell lysis. Here we develop a mathematical model of such an in vitro ADCC assay, formulated as a system of time-dependent ordinary differential equations and in which NK cells kill cancer cells at a rate which depends on the amount of antibody bound to each cancer cell. Numerical simulations generated using experimentally-based parameter estimates reveal that the system evolves on two timescales: a fast timescale on which antibodies bind to receptors on the surface of the tumour cells, and NK cells form complexes with the cancer cells, and a longer time-scale on which the NK cells kill the cancer cells. We construct approximate model solutions on each timescale, and show that they are in good agreement with numerical simulations of the full system. Our results show how the processes involved in ADCC change as the initial concentration of antibody and NK-cancer cell ratio are varied. We use these results to explain what information about the tumour cell kill rate can be extracted from the cytotoxicity assays.

摘要

免疫疗法利用免疫系统来靶向并杀死癌细胞,同时使健康组织免受损害。抗体疗法是一类重要的免疫疗法,它涉及抗体与肿瘤细胞表面特定抗原的结合,这些抗体可激活自然杀伤(NK)细胞以杀死肿瘤细胞。对可能引起抗体依赖性细胞毒性(ADCC)的分子进行临床前评估,需要在体外将癌细胞、NK细胞和抗体共同培养数小时,并测量随后的肿瘤细胞裂解水平。在此,我们建立了这样一种体外ADCC检测的数学模型,将其表述为一个与时间相关的常微分方程组,其中NK细胞以取决于与每个癌细胞结合的抗体量的速率杀死癌细胞。使用基于实验的参数估计进行的数值模拟表明,该系统在两个时间尺度上演变:一个快速时间尺度,在此期间抗体与肿瘤细胞表面的受体结合,NK细胞与癌细胞形成复合物;另一个较长的时间尺度,在此期间NK细胞杀死癌细胞。我们在每个时间尺度上构建了近似模型解,并表明它们与完整系统的数值模拟结果高度吻合。我们的结果展示了随着抗体初始浓度和NK-癌细胞比例的变化,ADCC所涉及的过程是如何改变的。我们利用这些结果来解释从细胞毒性检测中可以提取哪些关于肿瘤细胞杀伤率的信息。

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