Evidence map›Paper›PMID 32726880›Full record

ReviewJournal of leukocyte biology2020

Unraveling exhaustion in adaptive and conventional NK cells.

Aimee M Merino, Hansol Kim, Jeffrey S Miller, Frank Cichocki

Open access · greenAbstract readReview
In one paragraph

Review in Journal of leukocyte biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

43 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Single-cell RNA sequencing reveals anti-tumor potency of CD56Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  20. Article
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

4 authors at 1 institution in 1 country.

Aimee M MerinoDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0003-4433-0127
Hansol KimDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Jeffrey S MillerDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Frank CichockiDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
University of Minnesota · US

Funding

Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI John E. Wagner · 1995 to 2026
$48.2M
Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MILLER, JEFFREY S. · 2005 to 2025
$38.2M
TRAINING IN HEMOGLOBIN &CELL MEMBRANE RESEARCHT32HL007062 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller, Gregory M Vercellotti · 1985 to 2026
$10.3M
Viral priming and targeting NK cells against solid tumor malignanciesR35CA197292 · NCI · UNIVERSITY OF MINNESOTA · PI MILLER, JEFFREY S. · 2015 to 2021
$6.2M
Understanding and improving responses to adaptive NK cell therapy for leukemia and multiple myelomaK08CA255426 · NCI · UNIVERSITY OF MINNESOTA · PI MERINO, AIMEE · 2021 to 2025
$744k
Molecular Programming of Immunological Memory in Human Natural Killer CellsR00HL123638 · NHLBI · UNIVERSITY OF MINNESOTA · PI CICHOCKI, FRANK · 2017 to 2019
$736k
Molecular Programming of Immunological Memory in Human Natural Killer CellsK99HL123638 · NHLBI · UNIVERSITY OF MINNESOTA · PI CICHOCKI, FRANK · 2015 to 2016
$190k
NCI NIH HHS K08 CA255426NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412NCI NIH HHS R35 CA197292NHLBI NIH HHS K99 HL123638NHLBI NIH HHS R00 HL123638NHLBI NIH HHS T32 HL007062NIH HHS K99/R00 HL123638NIH HHS P01 CA111412NIH HHS P01 CA65493NIH HHS T32 2T32HL007062
6 · The paper itself

Abstract

Immune exhaustion in T cells significantly impacts their ability to control malignancies and infections, and its discovery has led to revolutionary therapies for cancer in the form of checkpoint blockade. NK cells, like T cells, are lymphocytes that recognize virally infected and malignantly transformed cells. However, it remains unclear if NK cells are similarly susceptible to exhaustion. In this review, the aims are to summarize what is currently known and to identify key areas of variability that skew the scientific literature on NK cell exhaustion. A lack of consensus on the defining features of NK cell dysfunctional states such as senescence, suppression, and exhaustion has made a comparison between studies difficult. There are also significant differences in the biology of NK cell subsets with long-lived, adaptive NK cells sharing an epigenetic signature closer to memory CD8

Indexed as

Adaptive ImmunityImmunologic MemoryCD8-Positive T-LymphocytesCellular SenescenceChronic DiseaseCytomegalovirusCytomegalovirus InfectionsHumansKiller Cells, Naturaladaptivecheckpoint receptorExhaustionLAG-3Natural KillerPD-1

Identifiers

PMID32726880
PMCPMC7722010
OpenAlexW3045781597

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.