Evidence map›Paper›PMID 27170644›Full record

ArticleClinical and vaccine immunology : CVI2016

Cytokine Profiles during Invasive Nontyphoidal Salmonella Disease Predict Outcome in African Children.

James J Gilchrist, Jennifer N Heath, Chisomo L Msefula, Esther N Gondwe, Vivek Naranbhai, Wilson Mandala, Jenny M MacLennan, Elizabeth M Molyneux, Stephen M Graham, Mark T Drayson and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. AlteredFrontiers in immunology · 2021
    Article
  3. Article
  4. Invasive NontyphoidalEcoSal Plus · 2019
    Review
  5. Review
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

12 authors at 7 institutions in 3 countries.

James J GilchristWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom Department of Paediatrics, University of Oxford, Oxford, United Kingdom.
Jennifer N HeathSchool of Immunity and Infection, College of Medicine and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Chisomo L MsefulaMalawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi Department of Microbiology, College of Medicine, University of Malawi, Blantyre, Malawi Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, United Kingdom.
Esther N GondweSchool of Immunity and Infection, College of Medicine and Dental Sciences, University of Birmingham, Birmingham, United Kingdom Malawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi Department of Microbiology, College of Medicine, University of Malawi, Blantyre, Malawi Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, United Kingdom.
Vivek NaranbhaiWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Wilson MandalaMalawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, United Kingdom.
Jenny M MacLennanMalawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi Department of Zoology, University of Oxford, Oxford, United Kingdom.
Elizabeth M MolyneuxDepartment of Paediatrics, College of Medicine, University of Malawi, Blantyre, Malawi.
Stephen M GrahamMalawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi Department of Paediatrics, College of Medicine, University of Malawi, Blantyre, Malawi Centre for International Child Health, University of Melbourne and Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Australia.
Mark T DraysonSchool of Immunity and Infection, College of Medicine and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Malcolm E MolyneuxMalawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, United Kingdom Department of Medicine, College of Medicine, University of Malawi, Blantyre, Malawi.
Calman A MacLennanSchool of Immunity and Infection, College of Medicine and Dental Sciences, University of Birmingham, Birmingham, United Kingdom Malawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, University of Malawi, Blantyre, Malawi Jenner Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom calman.maclennan@ndm.ox.ac.uk.
Malawi-Liverpool-Wellcome Trust Clinical Research Programme · MWUniversity of Birmingham · GBUniversity of Liverpool · GBUniversity of Malawi · MWUniversity of Oxford · GBCentre for Human Genetics · GBLiverpool School of Tropical Medicine · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Nontyphoidal Salmonella is a leading cause of sepsis in African children. Cytokine responses are central to the pathophysiology of sepsis and predict sepsis outcome in other settings. In this study, we investigated cytokine responses to invasive nontyphoidal Salmonella (iNTS) disease in Malawian children. We determined serum concentrations of 48 cytokines with multiplexed immunoassays in Malawian children during acute iNTS disease (n = 111) and in convalescence (n = 77). Principal component analysis and logistic regression were used to identify cytokine signatures of acute iNTS disease. We further investigated whether these responses are altered by HIV coinfection or severe malnutrition and whether cytokine responses predict inpatient mortality. Cytokine changes in acute iNTS disease were associated with two distinct cytokine signatures. The first is characterized by increased concentrations of mediators known to be associated with macrophage function, and the second is characterized by raised pro- and anti-inflammatory cytokines typical of responses reported in sepsis secondary to diverse pathogens. These cytokine responses were largely unaltered by either severe malnutrition or HIV coinfection. Children with fatal disease had a distinctive cytokine profile, characterized by raised mediators known to be associated with neutrophil function. In conclusion, cytokine responses to acute iNTS infection in Malawian children are reflective of both the cytokine storm typical of sepsis secondary to diverse pathogens and the intramacrophage replicative niche of NTS. The cytokine profile predictive of fatal disease supports a key role of neutrophils in the pathogenesis of NTS sepsis.

Indexed as

AdolescentChildChild, PreschoolCytokinesFemaleHIV InfectionsHumansInfantInfant, NewbornMacrophagesMalawiMaleMalnutritionNeutrophilsSalmonella InfectionsSepsisCytokines

Identifiers

PMID27170644
PMCPMC4933780
OpenAlexW2377270330

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.