Evidence map›Paper›PMID 30817998›Full record

ArticleClinical immunology (Orlando, Fla.)2019

Aberrant natural killer (NK) cell activation and dysfunction among ART-treated HIV-infected adults in an African cohort.

Rose Nabatanzi, Lois Bayigga, Stephen Cose, Sarah Rowland-Jones, Glenda Canderan, Moses Joloba, Damalie Nakanjako

Open access · hybridAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 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

7 authors at 4 institutions in 3 countries.

Rose NabatanziDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences, Kampala, Uganda.
Lois BayiggaDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences, Kampala, Uganda.
Stephen CoseMRC/UVRI and LSHTM Uganda Research Unit, Entebbe, Uganda; Department of Clinical Research, LSHTM, London, United Kingdom.
Sarah Rowland-JonesNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Glenda CanderanCase Western Reserve University, Cleveland, OH, USA.
Moses JolobaDepartment of Immunology and Molecular Biology, Makerere University College of Health Sciences, Kampala, Uganda.
Damalie NakanjakoDepartment of Medicine, Makerere University College of Health Sciences, Kampala, Uganda; Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda. Electronic address: dnakanjako@gmail.com.
Makerere University · UGCase Western Reserve University · USLondon School of Hygiene & Tropical Medicine · GBUniversity of Oxford · GB

Funding

Wellcome Trust 107743/Z/15/Z
6 · The paper itself

Abstract

backgroundWe examined NK cell phenotypes and functions after seven years of ART and undetectable viral loads (<50 copies/ml) with restored CD4 T-cell counts (≥500 cells/μl) and age-matched healthy-HIV-uninfected individuals from the same community.

methodsUsing flow-cytometry, NK cell phenotypes were described using lineage markers (CD56

resultsCD56 dim and CD56 bright NK cells were lower among ART-treated-HIV-infected than among age-matched-HIV-negative individuals; p = 0.0016 and p = 0.05 respectively. Production of CD107a (P = 0.004) and Granzyme-B (P = 0.005) was lower among ART-treated-HIV-infected relative to the healthy-HIV-uninfected individuals. NKG2D and NKp46 were lower, while CD69 expression was higher among ART-treated-HIV-infected than healthy-HIV-uninfected individuals.

conclusionNK cell activation and dysfunction persisted despite seven years of suppressive ART with "normalization" of peripheral CD4 counts.

Indexed as

AdultAntigens, CDAntigens, Differentiation, T-LymphocyteAnti-Retroviral AgentsBlack PeopleCD69 AntigensFemaleGranzymesHIV InfectionsHumansKiller Cells, NaturalLectins, C-TypeLymphocyte ActivationLysosomal-Associated Membrane Protein 1MaleMiddle AgedAntigens, CDAntigens, Differentiation, T-LymphocyteAnti-Retroviral AgentsCD69 AntigensGranzymesKLRK1 protein, humanLectins, C-TypeLysosomal-Associated Membrane Protein 1Natural Cytotoxicity Triggering Receptor 1NCR1 protein, humanNK Cell Lectin-Like Receptor Subfamily K107aAntiretroviral therapyGranzyme-BInterferon gammaNatural killer cellsNK cell activationNK cell dysfunctionNK Cytolytic functionNK degranulationNKG2DNKp46Sub-Saharan Africa

Identifiers

PMID30817998
PMCPMC6448528
OpenAlexW2916173084

What OpenQuestion holds

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Registered trials

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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.