Evidence map›Paper›PMID 36211403›Full record

SynthesisFrontiers in immunology2022

CD56-negative NK cells: Frequency in peripheral blood, expansion during HIV-1 infection, functional capacity, and KIR expression.

Alexander T H Cocker, Fuguo Liu, Zakia Djaoud, Lisbeth A Guethlein, Peter Parham

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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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 at 2 institutions in 2 countries.

Alexander T H CockerDepartment of Structural Biology and Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, United States.
Fuguo LiuDepartment of Structural Biology and Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, United States.
Zakia DjaoudDepartment of Structural Biology and Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, United States.
Lisbeth A GuethleinDepartment of Structural Biology and Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, United States.
Peter ParhamDepartment of Structural Biology and Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, United States.
Stanford University · USUniversity of Ottawa · CA

Funding

Functional genetics of human innate immunity in the bimodal gamma delta T cell response to Epstein-Barr Virus and in education of NK cells and their re-education to respond to autologous cellsR01AI136952 · NIAID · STANFORD UNIVERSITY · PI PARHAM, PETER R · 2019 to 2023
$2.0M
NIAID NIH HHS R01 AI136952
6 · The paper itself

Abstract

Human NK cells are usually defined as CD3

Indexed as

HIV-1HIV InfectionsCD56 AntigenHumansKiller Cells, NaturalPerforinReceptors, KIRCD56 AntigenPerforinReceptors, KIRCD56negchronic infectioninnate immunitymeta-analysisNK cells

Identifiers

PMID36211403
PMCPMC9539804
OpenAlexW4296995231

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.