Evidence map›Paper›PMID 10603404›Full record

ArticleInfection and immunity2000

Intracellular and extracellular cytokine production by human mixed mononuclear cells in response to group B streptococci.

D J Kwak, N H Augustine, W G Borges, J L Joyner, W F Green, H R Hill

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.2field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
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  10. World journal of transplantation · 2018
    Article
  11. Pneumonia.Seminars in fetal & neonatal medicine · 2017
    Review
  12. Article
  13. Article
  14. Article
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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

6 authors at 3 institutions in 2 countries.

D J KwakDepartment of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah 84132, USA.
N H Augustine
W G Borges
J L Joyner
W F Green
H R Hill
Pediatrics and Genetics · USHuntsman Cancer Institute · USUniversity of Utah · US

Funding

MECHANISMS OF HOST RESISTANCE TO GROUP B STREPTOCOCCIR01AI013150 · NIAID · UNIVERSITY OF UTAH · PI HILL, HARRY R · 1985 to 1999
–
NIAID NIH HHS AI 13150
6 · The paper itself

Abstract

Group B streptococci (GBS) are a major cause of severe infection in newborns, pregnant females, and other immunocompromised hosts. Infection often includes septicemia, shock, pneumonia, and respiratory failure. In previous studies, we have reported that GBS induce marked production of tumor necrosis factor alpha (TNF-alpha) by human mononuclear cells. The present study was designed to measure the production of TNF-alpha as well as additional cytokines, including interleukin 1beta (IL-1beta), IL-6, IL-8, IL-12, and gamma interferon (IFN-gamma) but also to determine from what cells and at what time point during incubation with GBS that these cytokines are produced. Mixed mononuclear cells were incubated with heat-killed GBS, media alone, or 1 microg of Escherichia coli lipopolysaccharide (LPS). Brefeldin A was added to each sample prior to staining, which prevented the export of cytokines by the Golgi apparatus. The cells were then stained with the appropriate conjugated antibodies and analyzed by using a flow cytometer. Results indicate that intracellular cytokines appear, in almost all cases, simultaneous to or before secreted proteins are detected. In contrast to the response to LPS, where TNF-alpha, IL-1beta, IL-6, and IL-8 appear almost simultaneously, the human monocyte response to GBS results in the production of TNF-alpha but delayed appearance of IL-1beta, IL-6, and IL-8. The lymphocyte response to GBS was also strikingly different from that to LPS in that both secreted IFN-gamma and IL-12 was detected, while LPS failed to induce production of these critical cytokines. This suggests an important role for TNF-alpha, IFN-gamma, and IL-12 in GBS pathogenesis and/or immunity.

Indexed as

AdultCytokinesExtracellular SpaceFemaleHumansImmunocompromised HostInfant, NewbornInterferon-gammaInterleukin-1Interleukin-12Interleukin-6Interleukin-8Intracellular FluidIn Vitro TechniquesLeukocytes, MononuclearLipopolysaccharidesCytokinesInterferon-gammaInterleukin-1Interleukin-12Interleukin-6Interleukin-8LipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID10603404
PMCPMC97137
OpenAlexW2159014182

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.