Evidence map›Paper›PMID 28767726›Full record

ArticlePloS one2017

High-resolution phenotyping identifies NK cell subsets that distinguish healthy children from adults.

Sanjana Mahapatra, Emily M Mace, Charles G Minard, Lisa R Forbes, Alexander Vargas-Hernandez, Teresa K Duryea, George Makedonas, Pinaki P Banerjee, William T Shearer, Jordan S Orange

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 69 citations in OpenAlex.

  1. Trial
  2. The HIV Reservoir and Immune Landscape Across the Life Course of Women: Implications for Cure Strategies.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
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  17. Human CD8Immune network · 2023
    Review
  18. Article
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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

10 authors at 2 institutions in 1 country.

Sanjana MahapatraDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, Texas, United States of America.
Emily M MaceDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, Texas, United States of America.
Charles G MinardDepartment of Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
Lisa R ForbesCenter for Human Immunobiology, Texas Children's Hospital, Houston, Texas, United States of America.
Alexander Vargas-HernandezDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, Texas, United States of America.
Teresa K DuryeaDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, United States of America.
George MakedonasDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, Texas, United States of America.
Pinaki P BanerjeeCenter for Human Immunobiology, Texas Children's Hospital, Houston, Texas, United States of America.
William T ShearerCenter for Human Immunobiology, Texas Children's Hospital, Houston, Texas, United States of America.
Jordan S OrangeDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, Texas, United States of America.ORCID http://orcid.org/0000-0001-7117-7725
Baylor College of Medicine · USTexas Children's Hospital · US

Funding

GENETIC, IMMUNOLOGIC AND MECHANISTIC BASIS OF HUMAN NK CELL DEFICIENCYR01AI120989 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ORANGE, JORDAN SCOTT · 2016 to 2025
$7.7M
Directing Function at the Natural Killer Cell Secretory Immunological SynapseR37AI067946 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Jordan Scott Orange · 2024 to 2026
$1.5M
NIAID NIH HHS R01 AI120989NIAID NIH HHS R37 AI067946
6 · The paper itself

Abstract

Natural killer (NK) cells are critical in immune defense against infected, stressed or transformed cells. Their function is regulated by the heterogeneous expression of a wide array of surface receptors that shape its phenotypic diversity. Although NK cells develop in the bone marrow and secondary lymphoid tissues, substantive differentiation is apparent in the peripheral blood including known age-related variation. In order to gain greater insight into phenotypic and functional variation within peripheral blood NK cells across age groups, we used multi-parametric, polyfunctional flow cytometry to interrogate the NK cell variability in 20 healthy adults and 15 5-10, 11-15 and 16-20 year-old children. We found that the normative ranges in both adults and children displayed great inter-individual variation for most markers. While the expression of several receptors did not differ, among those that did, the majority of the differences existed between adults and the three pediatric groups, rather than among children of different ages. Interestingly, we also identified variation in the individual expression of some markers by sex and ethnicity. Combinatorial analysis of NK cell receptors revealed intermediate subsets between the CD56bright and CD56dim NK cells. Furthermore, on examining the NK cell diversity by age, adults were discovered to have the lowest developmental diversity. Thus, our findings identify previously unappreciated NK cell subsets potentially distinguishing children from adults and suggest functional correlates that may have relevance in age-specific host defense.

Indexed as

ImmunophenotypingAdolescentAdultAge FactorsCD56 AntigenChildCluster AnalysisFemaleFlow CytometryHumansKiller Cells, NaturalLeukocytes, MononuclearMiddle AgedReceptors, Natural Killer CellYoung AdultCD56 AntigenReceptors, Natural Killer Cell

Identifiers

PMID28767726
PMCPMC5540415
OpenAlexW2739723356

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.