Hickling Timothy P, Chen Xiaoying, Vicini Paolo, Nayak Satyaprakash
Pharmacokinetics, Dynamics and Metabolism - New Biological Entities, Pfizer, Andover, MA, USA.
J Pharmacokinet Pharmacodyn. 2014 Oct;41(5):445-59. doi: 10.1007/s10928-014-9388-7. Epub 2014 Oct 19.
A key role of B cells in the mammalian immune response is the generation of antibodies that serve to protect the organism against antigenic challenges. The same process may also be detrimental in the context of autoimmunity. Several modeling approaches have been applied to this aspect of the immune response, from predicting potential epitopes to describing B cells progress through developmental models and simulating antibody production. Here we review some of the modeling techniques, and summarize models that describe different activation mechanisms for B cells, including T cell dependent and independent models. We focus on viral infection as a prototype system, and briefly describe case studies in other disease areas such as bacterial infection and oncology. We single out aspects of the B cell response for which there are current knowledge gaps. We outline areas in need of further research in modeling applications to ultimately produce a "B cell module" for a complete immune response model.
B细胞在哺乳动物免疫反应中的一个关键作用是产生抗体,这些抗体可保护机体抵御抗原挑战。在自身免疫的情况下,相同的过程可能也是有害的。几种建模方法已应用于免疫反应的这一方面,从预测潜在表位到通过发育模型描述B细胞的进展以及模拟抗体产生。在这里,我们回顾一些建模技术,并总结描述B细胞不同激活机制的模型,包括T细胞依赖性和非依赖性模型。我们将病毒感染作为一个原型系统进行重点研究,并简要描述其他疾病领域(如细菌感染和肿瘤学)的案例研究。我们指出了目前在B细胞反应方面存在知识空白的方面。我们概述了建模应用中需要进一步研究的领域,以便最终为完整的免疫反应模型生成一个“B细胞模块”。