Evidence map›Paper›PMID 36518759›Full record

ArticleFrontiers in immunology2022

Detailed phenotypic and functional characterization of CMV-associated adaptive NK cells in rhesus macaques.

Mohammad Zahidul Hasan, Charlotte Höltermann, Beatrix Petersen, Annette Schrod, Kerstin Mätz-Rensing, Artur Kaul, Gabriela Salinas, Ralf Dressel, Lutz Walter

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

9 authors at 2 institutions in 1 country.

Mohammad Zahidul HasanPrimate Genetics Laboratory, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
Charlotte HöltermannPrimate Genetics Laboratory, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
Beatrix PetersenPrimate Genetics Laboratory, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
Annette SchrodAnimal Husbandry, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
Kerstin Mätz-RensingPathology Unit, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
Artur KaulInfection Biology Unit, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
Gabriela SalinasNGS Core Unit for Integrative Genomics, Institute of Human Genetics, University Medical Center Göttingen, Göttingen, Germany.
Ralf DresselInstitute for Cellular and Molecular Immunology, University Medical Center Göttingen, Göttingen, Germany.
Lutz WalterPrimate Genetics Laboratory, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.
German Primate Center · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous research on adaptive NK cells in rhesus macaques suffered from the lack of specific antibodies to differentiate between inhibitory CD94/NKG2A and stimulatory CD94/NKG2C heterodimeric receptors. Recently we reported an expansion of NKG2C receptor-encoding genes in rhesus macaques, but their expression and functional role on primary NK cells remained unknown due to this deficit. Thus, we established monoclonal antibodies 4A8 and 7B1 which show identical specificities and bind to both NKG2C-1 and NKG2C-2 but neither react with NKG2C-3 nor NKG2A on transfected cells. Using a combination of 4A8 and Z199 antibodies in multicolor flow cytometry we detected broad expression (4-73%) of NKG2C-1 and/or NKG2C-2 (NKG2C-1/2) on primary NK cells in rhesus macaques from our breeding colony. Stratifying our data to CMV-positive and CMV-negative animals, we noticed a higher proportion (23-73%) of primary NK cells expressing NKG2C-1/2 in CMV+ as compared to CMV- macaques (4-5%). These NKG2C-1/2-positive NK cells in CMV+ macaques are characterized by lower expression of

Indexed as

Cytomegalovirus InfectionsNK Cell Lectin-Like Receptor Subfamily CAnimalsKiller Cells, NaturalMacaca mulattaNK Cell Lectin-Like Receptor Subfamily Cadaptive NK cellsCMVMamu-ENKG2ANKG2Crhesus macaque (Macaca mulatta)

Identifiers

PMID36518759
PMCPMC9742600
OpenAlexW4310232740

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.