Modeling flow cytometry data for cancer vaccine immune monitoring

被引:18
作者
Frelinger, Jacob [2 ]
Ottinger, Janet [3 ]
Gouttefangeas, Cecile [4 ]
Chan, Cliburn [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Biostat & Bioinformat, Durham, NC 27710 USA
[2] Duke Univ, Inst Genome Sci & Policy, Program Computat Biol & Bioinformat, Durham, NC 27708 USA
[3] Duke Univ, Med Ctr, Ctr AIDS Res, Durham, NC 27708 USA
[4] Univ Tubingen, Dept Immunol, D-72076 Tubingen, Germany
基金
美国国家卫生研究院;
关键词
Flow cytometry; Immune monitoring; Model-based analysis; Automation; Standardization; Markov chain Monte Carlo; HARMONIZATION GUIDELINES; QUALITY ASSESSMENT; PANEL; ASSAYS; CD4; OPTIMIZATION; ENUMERATION; CONSORTIUM; PROGRAM; 3-COLOR;
D O I
10.1007/s00262-010-0883-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Flow cytometry (FCM) is widely used in cancer research for diagnosis, detection of minimal residual disease, as well as immune monitoring and profiling following immunotherapy. In all these applications, the challenge is to detect extremely rare cell subsets while avoiding spurious positive events. To achieve this objective, it helps to be able to analyze FCM data using multiple markers simultaneously, since the additional information provided often helps to minimize the number of false positive and false negative events, hence increasing both sensitivity and specificity. However, with manual gating, at most two markers can be examined in a single dot plot, and a sequential strategy is often used. As the sequential strategy discards events that fall outside preceding gates at each stage, the effectiveness of the strategy is difficult to evaluate without laborious and painstaking back-gating. Model-based analysis is a promising computational technique that works using information from all marker dimensions simultaneously, and offers an alternative approach to flow analysis that can usefully complement manual gating in the design of optimal gating strategies. Results from model-based analysis will be illustrated with examples from FCM assays commonly used in cancer immunotherapy laboratories.
引用
收藏
页码:1435 / 1441
页数:7
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