Single-cell immune aging clocks reveal inter-individual heterogeneity during infection and vaccination.
Abstract
Aging affects human immune system functionality, increasing susceptibility to immune-mediated diseases. While gene expression programs accurately reflect immune function, their relationship with biological immune aging and health status remains unclear. Here we developed robust, cell-type-specific aging clocks (sc-ImmuAging) for the myeloid and lymphoid immune cell populations in circulation within peripheral blood mononuclear cells, using single-cell RNA-sequencing data from 1,081 healthy individuals aged from 18 to 97 years. Application of sc-ImmuAging to transcriptome data of patients with COVID-19 revealed notable age acceleration in monocytes, which decreased during recovery. Furthermore, inter-individual variations in immune aging induced by vaccination were identified, with individuals exhibiting elevated baseline interferon response genes showing age rejuvenation in CD8
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Research summary
The paper claims that single-cell immune aging clocks can reveal inter-individual heterogeneity in immune responses during infection and vaccination. This research is relevant as it addresses biological immune aging, which is a fundamental aspect of longevity and age-related health, potentially leading to insights that could improve immune function in aging populations.
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