Evidence map›Paper›PMID 40661537›Full record

ArticlebioRxiv : the preprint server for biology2025

Accumulation of SA-βGal-High Cells in Human Naïve T Cell Compartments Reveals a Stress-Adapted, Senescent-Like State.

Andreea Cristina Alexandru, Genesis Vega Hormazabal, Hiroyuki Matsui, Herbert Kasler, Sierra Lore, Carlos Galicia Aguirre, Andrea Roberts, Indra John Heckenbach, Ritesh Tiwari, Ryan Kwok and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Andreea Cristina AlexandruBuck Institute for Research on Aging.ORCID 0000-0002-9300-6246
Genesis Vega HormazabalBuck Institute for Research on Aging.
Hiroyuki MatsuiBuck Institute for Research on Aging.
Herbert KaslerBuck Institute for Research on Aging.
Sierra LoreBuck Institute for Research on Aging.ORCID 0009-0002-8446-8411
Carlos Galicia AguirreBuck Institute for Research on Aging.ORCID 0009-0002-9257-9576
Andrea RobertsBuck Institute for Research on Aging.
Indra John HeckenbachUniversity of Copenhagen.
Ritesh TiwariBuck Institute for Research on Aging.
Ryan KwokBuck Institute for Research on Aging.
Sydney BeckerBuck Institute for Research on Aging; University of California, Davis.
Eric VerdinBuck Institute for Research on Aging, Novato, CA, USA.ORCID 0000-0003-3703-3183

Funding

Cellular senescence and Associated Lysosomal Dysfunction in Immune AgingU01AI180158 · NIAID · BUCK INSTITUTE FOR RESEARCH ON AGING · PI Birgit Schilling, Eric M. Verdin · 2024 to 2026
$2.1M
NIAID NIH HHS U01 AI180158
6 · The paper itself

Abstract

Aging is associated with a decline in immune function termed immunosenescence, characterized by accumulation of senescent-like immune cells and chronic inflammation, known as inflammaging. While senescence-associated β-galactosidase (SA-βGal) activity is a well-established senescence marker, its functional significance and the precise cellular subsets affected within the T cell compartment remain unclear. Here, we identify and characterize a previously unrecognized subset of naïve CD4

Identifiers

PMID40661537
PMCPMC12259081

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.