Evidence map›Paper›PMID 28484464›Full record

ArticleFrontiers in immunology2017

Altered Natural Killer Cell Function in HIV-Exposed Uninfected Infants.

Christiana Smith, Emilie Jalbert, Volia de Almeida, Jennifer Canniff, Laurel L Lenz, Marisa M Mussi-Pinhata, Rachel A Cohen, Qilu Yu, Fabiana R Amaral, Jorge Pinto and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

31 citing papers in PubMed, 37 citations in OpenAlex.

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  11. T-SPOT.TB Reactivity in Southern African Children With and Without in Utero Human Immunodeficiency Virus Exposure.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
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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

13 authors at 7 institutions in 4 countries.

Christiana SmithDepartment of Pediatric Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, USA.
Emilie JalbertDepartment of Pediatric Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, USA.
Volia de AlmeidaFederal University of Sao Carlos Biological and Health Sciences Center, Sao Carlos, Brazil.
Jennifer CanniffDepartment of Pediatric Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, USA.
Laurel L LenzDepartment of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, USA.
Marisa M Mussi-PinhataDepartment of Pediatrics, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
Rachel A CohenWestat, Rockville, MD, USA.
Qilu YuWestat, Rockville, MD, USA.
Fabiana R AmaralDepartment of Pediatrics, Ribeirão Preto School of Medicine, University of São Paulo, São Paulo, Brazil.
Jorge PintoFederal University of Minas Gerais, Belo Horizonte, Brazil.
Jorge O AlarconInstituto de Medicina Tropical "Daniel A. Carrión" de la Universidad Nacional Mayor de San Marcos, Lima, Perú.
George SiberryMaternal and Pediatric Infectious Disease Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA.
Adriana WeinbergDepartment of Pediatric Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, USA.
University of Colorado Denver · USUniversidade de São Paulo · BRWestat (United States) · USEunice Kennedy Shriver National Institute of Child Health and Human Development · USNational University of San Marcos · PEUniversidade Federal de Minas Gerais · BRUniversidade Federal de São Carlos · BR

Funding

Immune Modulation by Bacterial AutolysinsR01AI065638 · NIAID · UNIVERSITY OF COLORADO DENVER · PI LENZ, LAUREL L · 2006 to 2016
$3.8M
NIAID NIH HHS R01 AI065638
6 · The paper itself

Abstract

objectivesHIV-exposed uninfected (HEU) infants have higher rates of severe and fatal infections compared with HIV-unexposed (HUU) infants, likely due to immune perturbations. We hypothesized that alterations in natural killer (NK) cell activity might occur in HEU infants and predispose them to severe infections.

designCase-control study using cryopreserved peripheral blood mononuclear cells (PBMCs) at birth and 6 months from HEU infants enrolled from 2002 to 2009 and HUU infants enrolled from 2011 to 2013.

methodsNK cell phenotype and function were assessed by flow cytometry after 20-h incubation with and without K562 cells.

resultsThe proportion of NK cells among PBMCs was lower at birth in 12 HEU vs. 22 HUU (1.68 vs. 10.30%,

conclusionNK cell proportion, phenotype, and function are altered in HEU infants. NK cell cytotoxicity and degranulation are increased in HEU at birth, but HEU NK cells have reduced IFNγ and perforin production, suggesting an adequate initial response, but decreased functional reserve. NK cell function improved with addition of exogenous IL-12, implicating impaired production of IL-12 by accessory cells. Alterations in NK cell and accessory cell function may contribute to the increased susceptibility to infection in HEU infants.

Indexed as

HIV-1infantinterleukin-12K562 cellsnatural killer cellsrespiratory tract infections

Identifiers

PMID28484464
PMCPMC5403425
OpenAlexW2609621218

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.