Evidence map›Paper›PMID 28119485›Full record

ArticleThe Journal of infectious diseases2017

Plasma Cytokines and Chemokines in Zambian Children With Measles: Innate Responses and Association With HIV-1 Coinfection and In-Hospital Mortality.

Wen-Hsuan W Lin, Ashley N Nelson, Judith J Ryon, William J Moss, Diane E Griffin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2017. 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
1.6field-weighted citation impact, top 18% 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, 20 citations in OpenAlex.

  1. Review
  2. What's going on with measles?Journal of virology · 2024
    Review
  3. Article
  4. TNF-α Limits Serological Memory by Disrupting the Bone Marrow Niche.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  5. Article
  6. Review
  7. Measles Virus Infects and Programs MAIT Cells for Apoptosis.The Journal of infectious diseases · 2021
    Article
  8. Measles immunity and immunosuppression.Current opinion in virology · 2021
    Review
  9. Review
  10. Article
  11. Current genomics · 2019
    Article
  12. Article
  13. Review
  14. 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

5 authors at 1 institution in 1 country.

Wen-Hsuan W LinW. Harry Feinstone Department of Molecular Microbiology and Immunology, Baltimore, Maryland, USA.
Ashley N NelsonW. Harry Feinstone Department of Molecular Microbiology and Immunology, Baltimore, Maryland, USA.
Judith J RyonW. Harry Feinstone Department of Molecular Microbiology and Immunology, Baltimore, Maryland, USA.
William J MossW. Harry Feinstone Department of Molecular Microbiology and Immunology, Baltimore, Maryland, USA.
Diane E GriffinW. Harry Feinstone Department of Molecular Microbiology and Immunology, Baltimore, Maryland, USA.
Johns Hopkins University · US

Funding

Training: Molecular & Cellular Bases of Infectious DiseasesT32AI007417 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Arturo Casadevall · 1994 to 2026
$11.9M
Immune Responses During Measles Virus InfectionR01AI023047 · NIAID · JOHNS HOPKINS UNIVERSITY · PI GRIFFIN, DIANE E · 1986 to 2007
$2.1M
Vitamin A-Mediated Protection in MeaslesR21AI095981 · NIAID · JOHNS HOPKINS UNIVERSITY · PI GRIFFIN, DIANE E · 2013 to 2014
$446k
NIAID NIH HHS R01 AI023047NIAID NIH HHS R21 AI095981NIAID NIH HHS T32 AI007417
6 · The paper itself

Abstract

To identify immune factors present during the acute rash phase of measles and associations with outcome and human immunodeficiency virus type 1 (HIV-1) coinfection, we measured the plasma levels of 22 cytokines and chemokines in Zambian children hospitalized with measles (n = 148) and control children (n = 44). Children with measles had higher levels of innate cytokines tumor necrosis factor (TNF) α, interleukin 1β (IL-1β), interleukin 18, and interleukin 6; chemokines CCL2, CCL4, CCL11, CCL22, CXCL8, and CXCL10; and T-cell cytokines interferon γ, and interleukin 2, 10, and 17. Children who died in the hospital had higher levels of TNF-α, IL-1β, interleukin 12p70; CCL2, CCL4, CCL13, CCL17, CXCL8, CXCL10; and interleukin 2 and interferon γ than children who survived, and lower levels of interleukin 4. Children coinfected with HIV-1 had higher levels of TNF-α and IL-1β than HIV-uninfected children with measles, and lower levels of interleukin 4 and 5. Therefore, acute measles was characterized by activation of macrophages and T cells producing type 1, but not type 2, cytokines, which was more pronounced in fatal disease.

Indexed as

Immunity, InnateChemokinesChild, PreschoolCoinfectionCytokinesFemaleHIV-1HIV InfectionsHospitalizationHospital MortalityHumansInfantMaleMeaslesZambiaChemokinesCytokinesinflammasomeinnate responsesmacrophage activationmeaslesNF-κB

Identifiers

PMID28119485
PMCPMC5388292
OpenAlexW2581608985

What OpenQuestion holds

Textmetadata
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.