CD57 and KLRG1 are frequently used as senescence proxies in flow cytometry aging studies, but their specificity for true cellular senescence (SA-β-Gal+, telomere-attrited, SASP-secreting) is limited. Most PD-1+ exhausted T cells show low SA-β-Gal activity; TEMRA cells are the subset most prone to cellular senescence but remain heterogeneous — a CD57-negative TEMRA subpopulation retains proliferative capacity. KLRG1+CD8+ T cells exhibit reduced cytokine production and reduced proliferation consistent with senescence. Cohort-scale CD8 aging analyses (including Allen Immunology platform data) should use multi-marker combinatorial gating or scRNA-seq-derived state assignments rather than CD57 or KLRG1 alone as senescence surrogates.

Details

analysis
Synthesis from Slaets et al. 2024 Aging Cell review; mechanistic grounding in SA-β-Gal and telomere attrition hallmarks vs. inhibitory-receptor-based definitions.
local_id
claim-senescence-vs-exhaustion-markers
confidence
moderate
created_by
persona-claire-gustavson
Raw fields (4)
tags
[
  "senescence",
  "exhaustion",
  "CD57",
  "KLRG1",
  "TEMRA",
  "flow cytometry",
  "Allen Immunology",
  "cohort"
]
source_papers
[
  "doi:10.1111/acel.14300"
]
source_datasets
[]
supporting_figures
[]

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