Evidence map›Paper›PMID 27718327›Full record

ArticleCytometry. Part B, Clinical cytometry2017

The newborn human NK cell repertoire is phenotypically formed but functionally reduced.

Dara M Strauss-Albee, Emily C Liang, Thanmayi Ranganath, Natali Aziz, Catherine A Blish

Abstract read
In one paragraph

Article in Cytometry. Part B, Clinical cytometry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  8. Review
  9. Article
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  13. COVID-19 in babies: Knowledge for neonatal care.Journal of neonatal nursing : JNN · 2020
    Review
  14. Article
  15. CXCR6Frontiers in immunology · 2019
    Article
  16. Review
  17. Review
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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.

Dara M Strauss-AlbeeImmunology Program, Stanford University School of Medicine, Stanford, California, 94305.
Emily C LiangDepartment of Medicine, Stanford University School of Medicine, Stanford, California, 94305.
Thanmayi RanganathDepartment of Medicine, Stanford University School of Medicine, Stanford, California, 94305.
Natali AzizDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, California, 94305.
Catherine A BlishImmunology Program, Stanford University School of Medicine, Stanford, California, 94305.

Funding

Modeling the influence of sex on natural killer cell networksDP2AI112193 · NIAID · STANFORD UNIVERSITY · PI BLISH, CATHERINE A · 2013 to 2015
$2.5M
Defining the Natural Killer Cell Response to HIVF31AI118469 · NIAID · STANFORD UNIVERSITY · PI STRAUSS-ALBEE, DARA · 2015 to 2015
$43k
NIAID NIH HHS DP2 AI112193NIAID NIH HHS F31 AI118469
6 · The paper itself

Abstract

backgroundInfection is a leading cause of death worldwide in babies under 1 month of age. Better vaccines and therapeutics are desperately needed for this vulnerable population.

methodsBecause newborns rely heavily on the innate immune system, we evaluated cell phenotype and function of some of the earliest cellular responders during infection, natural killer (NK) cells. We used mass cytometry to provide a comprehensive comparison of NK cells from umbilical cord blood and adult peripheral blood.

resultsIn unsupervised analyses, including viSNE and principal component analysis, the structure of the cord blood and adult NK cell repertoires are highly similar, distinguishable mainly by maturity-related markers expressed on rare subpopulations of cells. However, in functional analyses, cord blood NK cells show reduced degranulation and cytokine production following target recognition, as well as antibody-dependent cell-mediated cytotoxicity and apoptosis induction in targets.

conclusionsThese findings show that the structure of the NK cell repertoire is intact at birth, suggesting great potential for vaccine and therapeutic strategies targeting this cell population. © 2016 International Clinical Cytometry Society.

Indexed as

Flow CytometryAdultAntigens, CDCytotoxicity, ImmunologicFemaleFetal BloodHumansInfant, NewbornInterferon-gammaKiller Cells, NaturalMaleMiddle AgedYoung AdultAntigens, CDInterferon-gammamass cytometrynatural killer cellsumbilical cord bloodviSNE

Identifiers

PMID27718327
PMCPMC5300060

What OpenQuestion holds

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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.