Generalized linear modeling of flow cytometry data to analyze immune responses in tuberculosis vaccine research.

IF 3.5 2区 生物学 Q1 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Pablo Maldonado, Taru S Dutt, Amanda Hitpas, Brendan Podell, G Brooke Anderson, Marcela Henao-Tamayo
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引用次数: 0

Abstract

Tuberculosis (TB) caused by Mycobacterium tuberculosis (Mtb) kills ~1.3 million people annually. Accordingly, vaccines and sophisticated analytical tools are necessary to evaluate their effectiveness. To address these challenges, we created a Generalized Linear Model (GLM) framework to evaluate high-dimensional flow cytometry data and the multivariable influences on immune responses, accommodating proportional and non-normal data, and violations of assumptions set by classical statistical evaluations. In naïve mice vaccinated with BCG boosted with ID93-GLA-SE, we used GLMs to assess the impact of sex, vaccination, and days post-infection on probabilities of immune cell phenotypes following Mtb challenge. We demonstrate enhanced T cell responses in the lung following BCG + ID93-GLA-SE compared to BCG or ID93-GLA-SE alone, with notable sex differences in humoral immunity. This framework highlights GLMs in assessing complex datasets while enhancing our comprehension of independent continuous and categorical variables on vaccine efficacy, and serves as a foundation for deeper, more complex scenarios.

流式细胞术数据的广义线性建模以分析结核病疫苗研究中的免疫反应。
由结核分枝杆菌(Mtb)引起的结核病(TB)每年造成约130万人死亡。因此,需要疫苗和精密的分析工具来评估其效力。为了解决这些挑战,我们创建了一个广义线性模型(GLM)框架来评估高维流式细胞术数据和对免疫反应的多变量影响,适应比例和非正态数据,以及违反经典统计评估设定的假设。在接种了ID93-GLA-SE卡介苗的naïve小鼠中,我们使用glm来评估性别、疫苗接种和感染后天数对Mtb攻击后免疫细胞表型概率的影响。我们发现,与卡介苗或单独使用ID93-GLA-SE相比,卡介苗+ ID93-GLA-SE在肺部的T细胞应答增强,在体液免疫方面存在显著的性别差异。该框架突出了glm在评估复杂数据集方面的作用,同时增强了我们对疫苗效力的独立连续变量和分类变量的理解,并为更深入、更复杂的情景奠定了基础。
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来源期刊
NPJ Systems Biology and Applications
NPJ Systems Biology and Applications Mathematics-Applied Mathematics
CiteScore
5.80
自引率
0.00%
发文量
46
审稿时长
8 weeks
期刊介绍: npj Systems Biology and Applications is an online Open Access journal dedicated to publishing the premier research that takes a systems-oriented approach. The journal aims to provide a forum for the presentation of articles that help define this nascent field, as well as those that apply the advances to wider fields. We encourage studies that integrate, or aid the integration of, data, analyses and insight from molecules to organisms and broader systems. Important areas of interest include not only fundamental biological systems and drug discovery, but also applications to health, medical practice and implementation, big data, biotechnology, food science, human behaviour, broader biological systems and industrial applications of systems biology. We encourage all approaches, including network biology, application of control theory to biological systems, computational modelling and analysis, comprehensive and/or high-content measurements, theoretical, analytical and computational studies of system-level properties of biological systems and computational/software/data platforms enabling such studies.
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