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关注这篇论文的作者
Ollivier Hyrien
Martin S Zand

用于 CFSE 标记实验分析的相关观测混合模型

研究问题
在细胞分裂导致荧光标记观测相互依赖、且细胞簇归属无法识别的实验中,如何估计细胞增殖过程的相关参数?
方法与思路
作者用年龄依赖分枝过程指定混合比例,在存在相关观测的混合模型下提出三个估计量,并进行模拟与淋巴细胞应用。
材料陈述的贡献
摘要称,三个估计量具有一致性和渐近正态性,并比较其有限样本性质,用于分析两类 T 淋巴细胞的激活与增殖。
阅读关注点
应核对分枝过程与混合比例的联系、未识别簇造成的依赖结构,以及三个估计量的条件、计算方式和有限样本差异。
阅读边界
仅据版本未注明的索引摘要,三个估计量的具体形式、定理条件及生物学比较结果未说明,不能推断某一估计量普遍更优。

原文摘要

Recent advances in flow cytometry have resulted in the development of powerful bioassays to analyze the proliferation of cell populations. The carboxy-fluorescein diacetate succinimidyl ester (CFSE)-labeling experiment is one such assay that is widely used to study cell kinetics and as a standard tool for investigating lymphocyte proliferation. Several mathematical models have been proposed to describe cell proliferation during CFSE experiments. The statistical analysis of CFSE-labeling data has received little attention, but it poses a number of methodological issues. In this article we approach their analysis using a mixture model. The mixing proportions are specified through an age-dependent branching process that models the temporal organization of the cell population. Because the CFSE molecules are partitioned between daughter cells when their mother divides, the observations generated by this assay are dependent. The data structure can be compared with that of a partially observed random-effects model where the clusters cannot be identified. In this context, we propose three estimators. We prove their consistency and asymptotic normality, investigate their finite-sample properties in simulation studies, and contrast their relative merits for the analysis of CFSE-labeling data. We use the proposed methods to analyze the proliferation in vitro of CD4+ and CD8+ T lymphocytes. In particular, we compare their activation and proliferation rates, and also investigate the effect of two stimuli that activate resting lymphocytes: the nonspecific mitogen phytohemaglutanin (PHA) and ligation of both the T-cell receptor CD3 and the costimulatory receptor CD28 cell surface proteins with monoclonal antibodies.

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