Cohort
PMID 40945050
Controlled access
eBioMedicine ยท 2025 ยท DOI 10.1016/j.ebiom.2025.105922
๐ฃ CEN 31
offspring 17
ctl 26
scRNA-seq + TCR + CyTOF + flow
Across the Lingao, Rugao and Japan cohorts, ~230k cells show NK cells "rejuvenating" via RUNX3 and building an enhanced NKโT immune defence shield.
Show cohort findings
- NK cells significantly increased; B cells and CD4+ T reduced; offspring show intermediate state.
- NK cells show a 'young' profile (earlier differentiation trajectory, rejuvenated membrane receptors).
- Transcription factor RUNX3 upregulated in NK and CD4+ T (confirmed by flow).
- NKโT immune interaction enhanced via MHC-I antigen presentation, CD99 adhesion and MIF signalling.
Cohort
PMID 36354175
Controlled access
Advanced Science (Weinheim) ยท 2022 ยท DOI 10.1002/advs.202204849
๐ฃ CEN 7
offspring 6
ctl 9
scRNA-seq + TCR
Seven Rugao-living centenarians and their offspring share a consistent longevity immune remodeling: naive T cells recede, GZMB+/CMC1+ cytotoxic T cells accumulate with high TCR clonal expansion.
Show cohort findings
- Centenarians and offspring both show naive T (NPC) decrease and cytotoxic T (CPC) increase, mainly CD8+.
- CPC share enhanced immune signalling and high TCR clonal expansion in both centenarians and offspring.
- Enrichment of GZMB+ and CMC1+ CD8 T cells (rather than age-associated GZMK+ T cells).
- Points to a heritable, longevity-associated immune remodeling pattern for healthy aging.
Cohort
PMID 37005201
GEO TBD
eBioMedicine ยท 2023 ยท DOI 10.1016/j.ebiom.2023.104514
๐ฃ CEN 14
offspring 0
ctl 52
Multi-modal scRNA-seq + flow validation
One of the largest centenarian single-cell datasets, sketching 'elite immunity' โ centenarians retain a highly functional, B-cell-shifted adaptive immune signature after a lifetime of exposure.
Show cohort findings
- Age-related rise in myeloid/lymphoid ratio and in cytotoxic relative to non-cytotoxic cell fractions.
- Centenarians show a marked CD4+ T to B-cell shift, consistent with lifelong antigen exposure and recovery.
- Longevity-specific cell-type signatures incl. DNA-damage-response gene STK17A and centenarian-specific S100A4.
- Proposes an 'elite immunity' concept โ a highly functional immune system honed over a lifetime.
Cohort
PMID 37379396
GSE213516 open; SC not local
Science Advances ยท 2023 ยท DOI 10.1126/sciadv.abq7599
๐ฃ CEN 7
offspring 0
ctl 17
scRNA-seq + single-cell aging clock + ribosome-inhibition assay
A PBMC single-cell aging clock shows supercentenarians' physiological age ~19 y younger than their actual age, driven by a high-ribosome-translation, low-inflammation slow-aging balance.
Show cohort findings
- Supercentenarians' blood biological age 80.43โ102.67 y โ ~18.6 y younger than their ~110 mean actual age ('slow aging').
- More CD8+ naive, fewer cytotoxic T / memory CD4+ T / megakaryocytes; naiveโCTL polarization delayed.
- Core molecular feature: more cells with high ribosome levels โ high translation, low-inflammation state.
- Ribosome/translation inhibition in monocytes validates a 'translation against inflammation' balance.
Cohort
PMID 41784043
Public reuse ยท not local
Aging Cell ยท 2026 ยท DOI 10.1111/acel.70431
๐ฃ CEN โ
offspring โ
ctl โ
scRNA-seq (integrated) + bulk RNA-seq + Scissor + eQTL colocalization
Integrating East-Asian full-lifespan scRNA with Guangxi centenarian bulk, this atlas maps a "longevity molecular tag" โ a cytotoxic immune lineage led by NK, CD8+ and ฮณฮด T balanced by fine inflammatory tuning.
Show cohort findings
- Scissor+ cells (NK, CD8+ T, ฮณฮด T) show enhanced cytotoxic and immunomodulatory function.
- Scissorโ cells (CD4+ T, B, dendritic cells) associate with inflammatory signalling and Th17/Th1 differentiation.
- eQTL colocalization finds 5 longevity-associated loci (e.g. rs3793537โGLIPR2/CD72/TLN1, rs8019902โTRDV2/TRDC).
- Centenarians reshape the cytotoxic immune lineage and finely regulate inflammation to achieve immune balance.