Evidence map›Paper›PMID 9060839›Full record

ArticleThe American journal of pathology1997

Expression pattern and cellular origin of cytokines in the normal and Toxoplasma gondii-infected murine brain.

D Schlüter, N Kaefer, H Hof, O D Wiestler, M Deckert-Schlüter

Abstract read
In one paragraph

Article in The American journal of pathology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.0field-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

34 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. ThemBio · 2021
    Article
  3. Review
  4. Presence of Toxoplasma gondii infection in brain as a potential cause of risky behavior: a report of 102 autopsy cases.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Article
  5. Article
  6. RecombinantFrontiers in cellular and infection microbiology · 2017
    Article
  7. In vivo effect of anti-TNF agent (etanercept) in reactivation of latent toxoplasmosis.Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2016
    Article
  8. Psychiatric aspects of toxoplasmosis: an Indian perspective.Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2016
    Article
  9. Article
  10. Microglia development and function.Annual review of immunology · 2014
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Microglia in infectious diseases of the central nervous system.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2009
    Review
  18. Review
  19. Article
  20. 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.

D SchlüterInstitut für Medizinische Mikrobiologie und Hygiene, Universität Heidelberg, Mannheim, Germany.
N Kaefer
H Hof
O D Wiestler
M Deckert-Schlüter
Heidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the normal brain, low levels of cytokines are observed, whereas inflammatory disorders of the central nervous system are characterized by an up-regulation of cytokine production. The cellular sources for cytokines in the central nervous system are largely undefined. In the present study, we have analyzed intracerebral cytokine production in normal and Toxoplasma gondii-infected mice using immunohistochemistry, in situ hybridization, flow cytometry of brain-derived leukocytes, and reverse transcriptase polymerase chain reaction detection in various subpopulations of inflammatory cells. In the normal brain, neurons and choroid plexus epithelia expressed interleukin (IL)-1 beta and IL-10. Microglia/macrophages produced IL-1 beta, IL-10, and tumor necrosis factor-alpha In Toxoplasma encephalitis, these cell types exhibited increased levels of the respective cytokines. In addition, microglia/macrophages showed a de novo expression of inducible nitric oxide synthase. CD4+ and CD8+ T cells, which were recruited to the brain, produced IL-2, IL-10, tumor necrosis factor-alpha, and interferon-gamma. IL-4 was exclusively detectable in CD4+ T cells, whereas CD8+ T cells showed expression of IL-1 beta. As chronic Toxoplasma encephalitis was not associated with neuronal degeneration and an up-regulation of neurotrophic factors, some cytokines may also exert neurotrophic and/or neuroprotective properties.

Indexed as

AnimalsBase SequenceBrainCytokinesEncephalitisFemaleFlow CytometryImmunohistochemistryImmunomagnetic SeparationImmunophenotypingIn Situ HybridizationLymphocyte SubsetsMiceMice, Inbred BALB CNerve Growth FactorsPolymerase Chain ReactionCytokinesNerve Growth FactorsRNA, Messenger

Identifiers

PMID9060839
PMCPMC1857868
OpenAlexW1528893442

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.