Multi-omic profiling reveals age-related immune dynamics in healthy adults

The generation and maintenance of immunity is a dynamic process that is dependent on age<sup>1-3</sup>. Here, to better understand its progression, we profiled peripheral immunity in more than 300 healthy adults (25 to 90 years of age) using single-cell RNA sequencing, proteomics and flow cytometry, following 96 adults longitudinally across 2 years with seasonal influenza vaccination. The resulting resource generated a single-cell RNA-sequencing dataset of more than 16 million peripheral blood mononuclear cells with 71 immune cell subsets from our Human Immune Health Atlas and enabled us to interrogate how immune cell composition and states shift with age, chronic viral infection and vaccination. From these data, we demonstrate robust, non-linear transcriptional reprogramming in T cell subsets with age that is not driven by systemic inflammation or chronic cytomegalovirus infection. This age-related reprogramming led to a functional T helper 2 (T<sub>H</sub>2) cell bias in memory T cells that is linked to dysregulated B cell responses against highly boosted antigens in influenza vaccines. Collectively, this study reveals unique features of the immune ageing process that occur prior to advanced age and provides novel targets for age-related immune modulation. We provide interactive tools for exploring this extensive human immune health resource at https://apps.allenimmunology.org/aifi/insights/dynamics-imm-health-age/ .

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Publication Details

Journal
Nature
Published
2025-10-29
DOI
https://doi.org/10.1038/s41586-025-09686-5
Citations
16
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
12.90
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article

Multi-omic profiling reveals age-related immune dynamics in healthy adults

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16 citations
Nature
Single-cell and spatial transcriptomics
12.90
article

Multi-omic profiling reveals age-related immune dynamics in healthy adults

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article en
16 citations

Abstract

The generation and maintenance of immunity is a dynamic process that is dependent on age<sup>1-3</sup>. Here, to better understand its progression, we profiled peripheral immunity in more than 300 healthy adults (25 to 90 years of age) using single-cell RNA sequencing, proteomics and flow cytometry, following 96 adults longitudinally across 2 years with seasonal influenza vaccination. The resulting resource generated a single-cell RNA-sequencing dataset of more than 16 million peripheral blood mononuclear cells with 71 immune cell subsets from our Human Immune Health Atlas and enabled us to interrogate how immune cell composition and states shift with age, chronic viral infection and vaccination. From these data, we demonstrate robust, non-linear transcriptional reprogramming in T cell subsets with age that is not driven by systemic inflammation or chronic cytomegalovirus infection. This age-related reprogramming led to a functional T helper 2 (T<sub>H</sub>2) cell bias in memory T cells that is linked to dysregulated B cell responses against highly boosted antigens in influenza vaccines. Collectively, this study reveals unique features of the immune ageing process that occur prior to advanced age and provides novel targets for age-related immune modulation. We provide interactive tools for exploring this extensive human immune health resource at https://apps.allenimmunology.org/aifi/insights/dynamics-imm-health-age/ .

NatureVol. 648(8094)
Virginia Mason Medical Center (US), Children's Hospital of Philadelphia (US), Allen Institute for Immunology (US), Translational Therapeutics (United States) (US), Allen Institute (US), Benaroya Research Institute, University of Pennsylvania (US), Stanford University (US)
Openalex Percentile: Top 1%
Single-cell and spatial transcriptomics
12.90
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