Evidence map›Paper›PMID 10899844›Full record

ArticleInfection and immunity2000

Adaptive immunity against Listeria monocytogenes in the absence of type I tumor necrosis factor receptor p55.

D W White, V P Badovinac, X Fan, J T Harty

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Mechanisms of Memory T Cell Activation and Effective Immunity.Advances in experimental medicine and biology · 2015
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Listeria meningitis complicating infliximab treatment for Crohn's disease.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2005
    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 2 institutions in 1 country.

D W WhiteInterdisciplinary Graduate Program in Immunology, University of Iowa, Iowa City, Iowa 52242, USA.
V P Badovinac
X Fan
J T Harty
University of Iowa · USUniversity of Pennsylvania · US

Funding

Regulation of primary and secondary CD4 and CD8 T cell memoryR37AI042767 · NIAID · UNIVERSITY OF IOWA · PI HARTY, JOHN T · 2008 to 2017
$4.7M
T resident memory in the lungR01AI042767 · NIAID · UNIVERSITY OF IOWA · PI HARTY, JOHN T · 1998 to 2023
$4.4M
CD8+ T Cell effector mechanisms against L. monocytogenesR21AI042767 · NIAID · UNIVERSITY OF IOWA · PI HARTY, JOHN T. · 2002 to 2002
$331k
SPECIFICITY OF CD8 T CELLS AGAINST L MONOCYTOGENESR29AI036864 · NIAID · UNIVERSITY OF IOWA · PI HARTY, JOHN T. · 1995 to 1999
–
NIAID NIH HHS AI36864NIAID NIH HHS AI42767NIAID NIH HHS R01 AI042767NIAID NIH HHS R21 AI042767NIAID NIH HHS R37 AI042767
6 · The paper itself

Abstract

Tumor necrosis factor (TNF) and the type I TNF receptor (TNFRI), p55, are critical for resistance against primary infections with the intracellular bacterial pathogen Listeria monocytogenes. Importantly, however, susceptibility to primary listeriosis in cytokine-deficient mice does not preclude the development or expression of effective adaptive immunity against virulent L. monocytogenes. We used TNFRI(-/-) mice to study adaptive antilisterial immunity in the absence of interactions between TNF and TNFRI. Our experiments indicate that TNFRI(-/-) mice survive and clear high-dose challenges with an attenuated strain of L. monocytogenes that is incapable of cell-to-cell spread. Furthermore, TNFRI(-/-) mice immunized with attenuated L. monocytogenes go on to develop potent adaptive immunity to subsequent high-dose challenges with virulent L. monocytogenes. Interestingly, CD8(+) T-cell depletion in vivo inhibits immunity to L. monocytogenes in the spleen but not in the liver of TNFRI(-/-) mice. The adaptive immune response in these animals is characterized by activation of listeriolysin O-specific CD8(+) T cells, which are capable of transferring antilisterial immunity to naive wild-type C57BL/6 host mice. These experiments demonstrate the development and expression of potent CD8(+) T-cell-mediated antilisterial immunity in the absence of TNFRI.

Indexed as

Adaptation, BiologicalBacterial ToxinsVaccinationAdoptive TransferAnimalsAntigens, CDBacterial VaccinesCD8-Positive T-LymphocytesHeat-Shock ProteinsHemolysin ProteinsImmunity, CellularListeriosisLiverMiceMice, Inbred C57BLMice, Mutant StrainsAntigens, CDBacterial ToxinsBacterial VaccinesHeat-Shock ProteinsHemolysin ProteinshlyA protein, Listeria monocytogenesReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factor, Type I

Identifiers

PMID10899844
PMCPMC98351
OpenAlexW2101819101

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.