Evidence map›Paper›PMID 15271900›Full record

ArticleInfection and immunity2004

Gamma interferon production, but not perforin-mediated cytolytic activity, of T cells is required for prevention of toxoplasmic encephalitis in BALB/c mice genetically resistant to the disease.

Xisheng Wang, Hoil Kang, Takane Kikuchi, Yasuhiro Suzuki

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Variation in CD8 T cell IFNγ differentiation to strains ofFrontiers in cellular and infection microbiology · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Behavioral and Neuropathological Changes AfterFrontiers in cellular and infection microbiology · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Influence of the Host and Parasite Strain on the Immune Response DuringFrontiers in cellular and infection microbiology · 2020
    Review
  15. Penetration of CD8The American journal of pathology · 2019
    Article
  16. Article
  17. Article
  18. Frontiers in microbiology · 2018
    Article
  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

4 authors at 3 institutions in 1 country.

Xisheng WangCenter for Molecular Medicine and Infectious Diseases, Department of Biomedical Sciences and Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Hoil Kang
Takane Kikuchi
Yasuhiro Suzuki
Virginia–Maryland College of Veterinary Medicine · USStanford University · USVirginia Tech · US

Funding

Molecular immunopathogenesis of cerebral toxoplasmosisR01AI047730 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI SUZUKI, YASUHIRO · 2001 to 2005
$1.4M
TOXOPLASMOSIS: NATURE OF INFECTION AND IMMUNE RESPONSER01AI004717 · NIAID · PALO ALTO MEDICAL FOUNDATION RES INST · PI REMINGTON, JACK S · 1985 to 2001
$1.1M
TOXOPLASMOSIS: NATURE OF INFECTION AND IMMUNE RESPONSER37AI004717 · NIAID · PALO ALTO MEDICAL FOUNDATION RES INST · PI REMINGTON, JACK S · 1987 to 1996
–
NIAID NIH HHS AI04717NIAID NIH HHS AI 47730NIAID NIH HHS R01 AI047730
6 · The paper itself

Abstract

We previously showed the requirement of both T cells and gamma interferon (IFN-gamma)-producing non-T cells for the genetic resistance of BALB/c mice to the development of toxoplasmic encephalitis (TE). In order to define the role of IFN-gamma production and the perforin-mediated cytotoxicity of T cells in this resistance, we obtained immune T cells from spleens of infected IFN-gamma knockout (IFN-gamma(-/-)), perforin knockout (PO), and wild-type BALB/c mice and transferred them into infected and sulfadiazine-treated athymic nude mice, which lack T cells but have IFN-gamma-producing non-T cells. Control nude mice that had not received any T cells developed severe TE and died after discontinuation of sulfadiazine treatment due to the reactivation of infection. Animals that had received immune T cells from either wild-type or PO mice did not develop TE and survived. In contrast, nude mice that had received immune T cells from IFN-gamma(-/-) mice developed severe TE and died as early as control nude mice. T cells obtained from the spleens of animals that had received either PO or wild-type T cells produced large amounts of IFN-gamma after stimulation with Toxoplasma gondii antigens in vitro. In addition, the amounts of IFN-gamma mRNA expressed in the brains of PO T-cell recipients did not differ from those in wild-type T-cell recipients. Furthermore, PO mice did not develop TE after infection, and their IFN-gamma production was equivalent to or higher than that of wild-type animals. These results indicate that IFN-gamma production, but not perforin-mediated cytotoxic activity, by T cells is required for the prevention of TE in genetically resistant BALB/c mice.

Indexed as

Adoptive TransferAnimalsBrainEncephalitisFemaleHumansImmunity, InnateInterferon-gammaMembrane GlycoproteinsMiceMice, Inbred BALB CMice, NudePerforinPore Forming Cytotoxic ProteinsT-LymphocytesToxoplasmaInterferon-gammaMembrane GlycoproteinsPerforinPore Forming Cytotoxic Proteins

Identifiers

PMID15271900
PMCPMC470633
OpenAlexW2134957541

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.