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基于短时间体外扩增和改进的泊松分布分析估计抗原特异性 CD4+ T 细胞的频率和区间频率。

Estimating point and interval frequency of antigen-specific CD4+ T cells based on short in vitro expansion and improved poisson distribution analysis.

机构信息

Tumor Immunology Unit, San Raffaele Scientific Institute, Milan, Italy.

出版信息

PLoS One. 2012;7(8):e42340. doi: 10.1371/journal.pone.0042340. Epub 2012 Aug 7.

Abstract

BACKGROUND

Knowledge of antigen-specific CD4(+) T cells frequencies is pivotal to the choice of the antigen to be used in anti-viral and anti-tumor vaccination procedures and for monitoring of immune responses. Methods that employ small cell numbers from patient samples, are easy to perform and do not require complex techniques/instrumentations and therefore standardization are desirable.

METHODOLOGY/PRINCIPAL FINDINGS: Purified blood CD4(+) T cells from healthy donors were cultured with autologous antigen presenting cells in several replicate wells in equal numbers in the absence (un-stimulated wells) or in the presence of synthetic peptides corresponding to viral antigens promiscuous HLA-DR epitopes (antigen-stimulated wells). At day 7 of culture low dose IL-2 was added and at day 14 IFN-γ and IL-5 release in the supernatant was measured. A statistical analysis approach, based on Poisson distribution, was then implemented to calculate the frequency of viral-specific CD4(+) T cells. We first determined a patient-specific exceptionality threshold of cytokine release in the un-stimulated wells and then, based on this threshold, we counted the inactive/active wells within the antigen-stimulated wells. This number, along with the number of cells per well, allowed the point and interval estimates of frequencies. A ready-to-use Excel worksheet template with automatic calculations for frequencies estimate was developed and is provided as a supplemental file (Table S9).

CONCLUSIONS/SIGNIFICANCE: We report a simple experimental procedure combining short term in vitro cell culture with statistical analysis to calculate the frequency of antigen-specific CD4(+) T cells. The detailed experimental procedure along with the Excel applicative are a valuable tool for monitoring immune responses in the clinical practice.

摘要

背景

对抗原特异性 CD4(+) T 细胞频率的了解对于选择用于抗病毒和抗肿瘤疫苗接种程序的抗原以及监测免疫反应至关重要。那些采用来自患者样本的少量细胞、易于操作且不需要复杂技术/仪器的方法,因此理想情况下需要进行标准化。

方法

从健康供体中纯化血液 CD4(+) T 细胞,在多个重复孔中以相等数量与自体抗原呈递细胞共培养,在不存在(未刺激孔)或存在对应于病毒抗原的合成肽(抗原刺激孔)的情况下。在培养的第 7 天添加低剂量 IL-2,在第 14 天测量上清液中 IFN-γ和 IL-5 的释放。然后实施基于泊松分布的统计分析方法来计算病毒特异性 CD4(+) T 细胞的频率。我们首先确定了未刺激孔中细胞因子释放的患者特异性异常阈值,然后基于该阈值,我们计算了抗原刺激孔内的非活性/活性孔数。这个数字,以及每个孔中的细胞数量,允许对频率进行点估计和区间估计。我们开发了一个带有自动计算功能的现成 Excel 工作表模板,用于估计频率,并作为补充文件提供(表 S9)。

结论

我们报告了一种简单的实验程序,将短期体外细胞培养与统计分析相结合,以计算抗原特异性 CD4(+) T 细胞的频率。详细的实验程序以及 Excel 应用程序是在临床实践中监测免疫反应的有价值的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e95/3413706/f71d7532c7e6/pone.0042340.g001.jpg

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