Evidence map›Paper›PMID 21329693›Full record

ArticleInternational journal for parasitology2011

Toxoplasma gondii inhibits granzyme B-mediated apoptosis by the inhibition of granzyme B function in host cells.

Tatsuya Yamada, Tadakimi Tomita, Louis M Weiss, Amos Orlofsky

Open access · greenAbstract read
In one paragraph

Article in International journal for parasitology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Vaccines · 2025
    Review
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  4. Heliyon · 2023
    Review
  5. Review
  6. Article
  7. Article
  8. BioMed research international · 2019
    Review
  9. Mechanisms of Human Innate Immune Evasion byFrontiers in cellular and infection microbiology · 2019
    Review
  10. Host-Frontiers in immunology · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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 1 institution in 1 country.

Tatsuya YamadaDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Tadakimi Tomita
Louis M Weiss
Amos Orlofsky
Albert Einstein College of Medicine · US

Funding

Immunology/Pathology CoreP30AI051519 · NIAID · YESHIVA UNIVERSITY · PI GOLDSTEIN, HARRIS · 2003 to 2013
$18.6M
Toxoplasma encephalitis in AIDS:Bradyzoite RegulationsR01AI039454 · NIAID · YESHIVA UNIVERSITY · PI WEISS, LOUIS M. · 1996 to 2009
$3.1M
Regulation of Macrophage Cell Death by Toxoplasma gondiiR01AI055358 · NIAID · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI ORLOFSKY, AMOS Z · 2004 to 2008
$2.0M
NIAID NIH HHS AI-39454NIAID NIH HHS AI-51519NIAID NIH HHS AI-55358NIAID NIH HHS P30 AI051519NIAID NIH HHS R01 AI039454NIAID NIH HHS R01 AI055358
6 · The paper itself

Abstract

Host defense to the apicomplexan parasite Toxoplasma gondii is critically dependent on CD8(+) T cells, whose effector functions include the induction of apoptosis in target cells following the secretion of granzyme proteases. Here we demonstrate that T. gondii induces resistance of host cells to apoptosis induced by recombinant granzyme B. Granzyme B induction of caspase-independent cytochrome c release was blocked in T. gondii-infected cells. Prevention of apoptosis could not be attributed to altered expression of the Bcl-2 family of apoptotic regulatory proteins, but was instead associated with reduced granzyme B-mediated, caspase-independent cleavage of procaspase 3 to the p20 form in T. gondii-infected cells, as well as reduced granzyme B-mediated cleavage of the artificial granzyme B substrate, GranToxiLux. The reduction in granzyme B proteolytic function in T. gondii-infected cells could not be attributed to altered granzyme B uptake or reduced trafficking of granzyme B to the cytosol, implying a T. gondii-mediated inhibition of granzyme B activity. Apoptosis and GranToxiLux cleavage were similarly inhibited in T. gondii-infected cells exposed to the natural killer-like cell line YT-1. The endogenous granzyme B inhibitor PI-9 was not up-regulated in infected cells. We believe these findings represent the first demonstration of granzyme B inhibition by a cellular pathogen and indicate a new modality for host cell protection by T. gondii that may contribute to parasite immune evasion.

Indexed as

ApoptosisAnimalsCaspase 3CD8-Positive T-LymphocytesCell LineGranzymesHumansImmune EvasionToxoplasmaCaspase 3Granzymes

Identifiers

PMID21329693
PMCPMC3116727
OpenAlexW2018932831

What OpenQuestion holds

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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.