细胞毒性T淋巴细胞与肿瘤细胞相互作用的数学模型。与主要组织相容性复合物相关的小鼠嵌合b细胞淋巴瘤的生长、稳定和消退分析。

Biomedical science Pub Date : 1991-01-01
V A Kuznetsov
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引用次数: 0

摘要

提出了细胞毒性T淋巴细胞(CTL)对免疫原性肿瘤非指数生长反应的数学模型。该模型令人满意地描述了与主要组织相容性复合体(H-2b----H-2d)嵌合的小鼠脾脏B淋巴瘤BCL1的生长和消退动力学。描述不能在体内测量的过程的参数的数值估计已经导出。据预测,肿瘤的发展和它的临床表现有一个周期三到四个月的复发概况。根据该模型,BCL1肿瘤的有限生长及其进入休眠状态与肿瘤中CTL的高积累率,淋巴瘤细胞的快速裂解以及肿瘤细胞无法抑制细胞毒性淋巴细胞的影响功能有关。该模型还能够表现肿瘤“潜行”现象和肿瘤生长的免疫刺激。
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A mathematical model for the interaction between cytotoxic T lymphocytes and tumour cells. Analysis of the growth, stabilization, and regression of a B-cell lymphoma in mice chimeric with respect to the major histocompatibility complex.

A mathematical model of the response of cytotoxic T lymphocytes (CTL) to the nonexponential growth of an immunogenic tumour is presented. The model describes satisfactorily the kinetics of growth and regression of the B lymphoma BCL1 in the spleen of mice chimeric with respect to the major histocompatibility complex (H-2b----H-2d). Numerical estimations of the parameters describing processes that cannot be measured in vivo have been derived. It is predicted that the development of the tumour and its clinical manifestation have a recurrent profile with a cycle of three to four months. According to the model the limited growth of the BCL1 tumour and its transition into the dormant state are associated with a high rate of accumulation of CTL in the tumour, rapid lysis of lymphoma cells, and the inability of tumour cells to suppress the affector functions of cytotoxic lymphocytes. The model is also capable of representing the phenomenon of tumours 'sneaking through' and the immunostimulation of tumour growth.

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