Evidence map›Paper›PMID 26850637›Full record

ReviewCancer immunology, immunotherapy : CII2016

CD57 in human natural killer cells and T-lymphocytes.

Hassen Kared, Serena Martelli, Tze Pin Ng, Sylvia L F Pender, Anis Larbi

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers.

0numbers the graph read from it
0cells of the map it votes in
183citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

183 citing papers in PubMed, 314 citations in OpenAlex.

  1. Trial
  2. A Phase II Window of Opportunity Study of Neoadjuvant PD-L1 versus PD-L1 plus CTLA-4 Blockade for Patients with Malignant Pleural Mesothelioma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Trial
  3. Trial
  4. Trial
  5. βBrain, behavior, and immunity · 2018
    Trial
  6. Co-inhibitory profile and cytotoxicity of CD57Clinical and experimental immunology · 2018
    Trial
  7. Trial
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
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  17. Article
  18. Article
  19. Article
  20. Cytotoxic CD4Signal transduction and targeted therapy · 2026
    Review

123 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 2 countries.

Hassen KaredSingapore Immunology Network (SIgN), Aging and Immunity Program, Agency for Science Technology and Research (A*STAR), 8A Biomedical Grove #3 Immunos, Singapore, 138648, Republic of Singapore. hassen_kared@immunol.a-star.edu.sg.
Serena MartelliSingapore Immunology Network (SIgN), Aging and Immunity Program, Agency for Science Technology and Research (A*STAR), 8A Biomedical Grove #3 Immunos, Singapore, 138648, Republic of Singapore.
Tze Pin NgGerontological Program, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Republic of Singapore.
Sylvia L F PenderAcademic Unit of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Anis LarbiSingapore Immunology Network (SIgN), Aging and Immunity Program, Agency for Science Technology and Research (A*STAR), 8A Biomedical Grove #3 Immunos, Singapore, 138648, Republic of Singapore.
Agency for Science, Technology and Research · SGNational University of Singapore · SGSingapore Immunology Network · SGUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD57 antigen (alternatively HNK-1, LEU-7, or L2) is routinely used to identify terminally differentiated 'senescent' cells with reduced proliferative capacity and altered functional properties. In this article, we review current understanding of the attributes of CD57-expressing T-cells and NK cells in both health and disease and discuss how this marker can inform researchers about their likely functions in human blood and tissues in vivo. While CD57 expression on human lymphocytes indicates an inability to proliferate, these cells also display high cytotoxic potential, and CD57(pos) NK cells exhibit both memory-like features and potent effector functions. Accordingly, frequencies of CD57-expressing cells in blood and tissues have been correlated with clinical prognosis in chronic infections or various cancers and with human aging. Functional modulation of senescent CD57(pos) T-cells and mature CD57(pos) NK cells may therefore represent innovative strategies for protection against human immunological aging and/or various chronic diseases.

Indexed as

Arthritis, RheumatoidAutoimmune DiseasesCD57 AntigensCD8-Positive T-LymphocytesCell DifferentiationCytotoxicity, ImmunologicHumansKiller Cells, NaturalModels, ImmunologicalNeoplasmsCD57 AntigensCD57KLRG1Memory NK cellsNKG2CNK maturationSenescence

Identifiers

PMID26850637
PMCPMC11029668
OpenAlexW2267395364

What OpenQuestion holds

Textmetadata
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.