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衰老免疫系统的高维分析:健康供体中免疫信号反应与年龄相关差异的验证

High-dimensional analysis of the aging immune system: verification of age-associated differences in immune signaling responses in healthy donors.

作者信息

Longo Diane M, Louie Brent, Ptacek Jason, Friedland Greg, Evensen Erik, Putta Santosh, Atallah Michelle, Spellmeyer David, Wang Ena, Pos Zoltan, Marincola Francesco M, Schaeffer Andrea, Lukac Suzanne, Railkar Radha, Beals Chan R, Cesano Alessandra, Carayannopoulos Leonidas N, Hawtin Rachael E

机构信息

Nodality, South San Francisco, CA 94080, USA.

出版信息

J Transl Med. 2014 Jun 21;12:178. doi: 10.1186/1479-5876-12-178.

Abstract

BACKGROUND

Single-cell network profiling (SCNP) is a multiparametric flow cytometry-based approach that simultaneously measures evoked signaling in multiple cell subsets. Previously, using the SCNP approach, age-associated immune signaling responses were identified in a cohort of 60 healthy donors.

METHODS

In the current study, a high-dimensional analysis of intracellular signaling was performed by measuring 24 signaling nodes in 7 distinct immune cell subsets within PBMCs in an independent cohort of 174 healthy donors [144 elderly (>65 yrs); 30 young (25-40 yrs)].

RESULTS

Associations between age and 9 immune signaling responses identified in the previously published 60 donor cohort were confirmed in the current study. Furthermore, within the current study cohort, 48 additional immune signaling responses differed significantly between young and elderly donors. These associations spanned all profiled modulators and immune cell subsets.

CONCLUSIONS

These results demonstrate that SCNP, a systems-based approach, can capture the complexity of the cellular mechanisms underlying immunological aging. Further, the confirmation of age associations in an independent donor cohort supports the use of SCNP as a tool for identifying reproducible predictive biomarkers in areas such as vaccine response and response to cancer immunotherapies.

摘要

背景

单细胞网络分析(SCNP)是一种基于多参数流式细胞术的方法,可同时测量多个细胞亚群中的诱发信号。此前,使用SCNP方法在60名健康供体队列中鉴定出了与年龄相关的免疫信号反应。

方法

在本研究中,通过测量174名健康供体独立队列(144名老年人(>65岁);30名年轻人(25 - 40岁))外周血单核细胞中7个不同免疫细胞亚群的24个信号节点,对细胞内信号进行了高维分析。

结果

本研究证实了先前发表的60名供体队列中鉴定出的年龄与9种免疫信号反应之间的关联。此外,在本研究队列中,年轻和老年供老年供体之间另有48种免疫信号反应存在显著差异。这些关联涵盖了所有分析的调节因子和免疫细胞亚群。

结论

这些结果表明,基于系统的方法SCNP能够捕捉免疫衰老背后细胞机制的复杂性。此外,在独立供体队列中对年龄关联的证实支持将SCNP用作在疫苗反应和癌症免疫治疗反应等领域识别可重复预测生物标志物的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/214e/4229969/e5ed8e6a3a3f/1479-5876-12-178-1.jpg

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