Evidence map›Paper›PMID 20932941›Full record

ReviewAgeing research reviews2011

Expansions of NK-like αβT cells with chronologic aging: novel lymphocyte effectors that compensate for functional deficits of conventional NK cells and T cells.

Abbe N Vallejo, Robert G Mueller, David L Hamel, Amanda Way, Jeffrey A Dvergsten, Patricia Griffin, Anne B Newman

Open access · greenAbstract readReview
In one paragraph

Review in Ageing research reviews, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
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

26 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Divide, Conquer, and Sense: CD8Frontiers in immunology · 2016
    Article
  20. Adaptive Memory of Human NK-like CD8Frontiers in immunology · 2016
    Review
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

7 authors at 3 institutions in 1 country.

Abbe N VallejoChildren's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA 15224, USA. andv26@pitt.edu
Robert G Mueller
David L Hamel
Amanda Way
Jeffrey A Dvergsten
Patricia Griffin
Anne B Newman
University of Pittsburgh · USChildren's Hospital of Pittsburgh · USMcGowan Institute for Regenerative Medicine · US

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JENNIFER S BRACH · 2004 to 2026
$28.6M
Pathways of T cell SenescenceR01AG022379 · NIA · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI DE VALLEJO, ABBE N · 2003 to 2009
$1.8M
Immunity and Healthy AgingR01AG030734 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DE VALLEJO, ABBE N · 2009 to 2010
$1.8M
NCATS NIH HHS UL1 TR000005NIA NIH HHS P30 AG024827NIA NIH HHS R01 AG022379NIA NIH HHS R01 AG030734
6 · The paper itself

Abstract

As the repertoire of αβT cell receptors (TCR) contracts with advancing age, there is an associated age-dependent accumulation of oligoclonal T cells expressing of a variety of receptors (NKR), normally expressed on natural killer (NK) cells. Evidences for differential regulation of expression of particular NKRs between T cells and NK cells suggest that NKR expression on T cells is physiologically programmed rather than a random event of the aging process. Experimental studies show NKRs on aged αβT cells may function either as independent receptors, and/or as costimulatory receptors to the TCR. Considering the reported deficits of conventional αβTCR-driven activation and also functional deficits of classical NK cells, NKR(+) αβT cells likely represent novel immune effectors that are capable of combining innate and adaptive functions. Inasmuch as immunity is a determinant of individual fitness, the type and density of NKRs could be important contributing factors to the wide heterogeneity of health characteristics of older adults, ranging from institutionalized frail elders who are unable to mount immune responses to functionally independent community-dwelling elders who exhibit protective immunity. Understanding the biology of NKR(+) αβT cells could lead to new avenues for age-specific intervention to improve protective immunity.

Indexed as

Adaptive ImmunityAgedAged, 80 and overAgingHumansImmunity, InnateKiller Cells, NaturalReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID20932941
PMCPMC3039714
OpenAlexW2070991725

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.