Chao Dennis L, Davenport Miles P, Forrest Stephanie, Perelson Alan S
Department of Computer Science, University of New Mexico, Albuquerque, NM 87131, USA.
J Theor Biol. 2004 May 21;228(2):227-40. doi: 10.1016/j.jtbi.2003.12.011.
We have constructed a stochastic stage-structured model of the cytotoxic T lymphocyte (CTL) response to antigen and the maintenance of immunological memory. The model follows the dynamics of a viral infection and the stimulation, proliferation, and differentiation of naïve CD8(+) T cells into effector CTL, which can eliminate virally infected cells. The model is capable of following the dynamics of multiple T cell clones, each with a T cell receptor represented by a digit string. MHC-viral peptide complexes are also represented by strings and a string match rule is used to compute the affinity of a T cell receptor for a viral epitope. The avidities of interactions are also computed by taking into consideration the density of MHC-viral peptides on the surface of an infected cell. Lastly, the model allows the probability of T cell stimulation to depend on avidity but also incorporates the notion of an antigen-independent programmed proliferative response. We compare the model to experimental data on the cytotoxic T cell response to lymphocytic choriomeningitis virus infections.
我们构建了一个细胞毒性T淋巴细胞(CTL)对抗原反应及免疫记忆维持的随机阶段结构模型。该模型追踪病毒感染的动态过程以及初始CD8(+) T细胞刺激、增殖并分化为效应CTL的过程,效应CTL能够清除病毒感染细胞。该模型能够追踪多个T细胞克隆的动态变化,每个克隆的T细胞受体由数字串表示。MHC-病毒肽复合物也由字符串表示,并且使用字符串匹配规则来计算T细胞受体对病毒表位的亲和力。相互作用的亲和力还通过考虑感染细胞表面MHC-病毒肽的密度来计算。最后,该模型允许T细胞刺激的概率取决于亲和力,但也纳入了抗原非依赖性程序性增殖反应的概念。我们将该模型与关于细胞毒性T细胞对淋巴细胞性脉络丛脑膜炎病毒感染反应的实验数据进行了比较。