Evidence map›Paper›PMID 9712760›Full record

ArticleInfection and immunity1998

Fas (CD95)-dependent cell-mediated immunity to Listeria monocytogenes.

E R Jensen, A A Glass, W R Clark, E J Wing, J F Miller, S H Gregory

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Review
  3. CTLs: Killers of intracellular bacteria.Frontiers in cellular and infection microbiology · 2022
    Review
  4. Innate and Adaptive Immune Responses duringMicrobiology spectrum · 2019
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. From hot dogs to CD8+ T cells: Listeria monocytogenes.Transactions of the American Clinical and Climatological Association · 2000
    Review
  18. 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

6 authors at 3 institutions in 2 countries.

E R JensenDepartments of Microbiology and Immunology, University of California at Los Angeles, Los Angeles, California 90095, USA.
A A Glass
W R Clark
E J Wing
J F Miller
S H Gregory
University of California, Los Angeles · USUniversity of Pittsburgh Medical Center · USBipar · FR

Funding

MULTIDISCIPLINARY TRAINING IN MICROBIAL PATHOGENESIST32AI007323 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Peter John Bradley · 1988 to 2026
$8.6M
CLINICAL AND FUNDAMENTAL IMMUNOLOGYT32AI007126 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAXON, ANDREW · 1985 to 2006
$1.5M
FACTORS EFFECTING HEPATOCYTE RESISTANCE TO INFECTIONR01DK044367 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GREGORY, STEPHEN H. · 1994 to 1996
–
L MONOCYTOGENES AS A LIVE VACCINE VEHICLER21AI038955 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MILLER, JEFFERY F. · 1996 to 1996
–
NIAID NIH HHS AI32512-03NIAID NIH HHS AI38955NIAID NIH HHS T32 AI007126NIAID NIH HHS T32 AI007323NIDDK NIH HHS DK44367
6 · The paper itself

Abstract

Two distinct and complementary pathways, one mediated by perforin and the other dependent upon CD95 (Fas), effect cell-mediated cytotoxicity. We examined the relative roles of these pathways in host defenses against the intracellular bacterial pathogen Listeria monocytogenes by using murine listeriosis as a model system. Mice which lacked both perforin and Fas (P0L0) were generated, and their responses to primary and secondary listeriosis were compared to those of wild-type (WT), Fas-deficient (L0), and perforin knockout (P0) mice. Relative to WT mice during primary listeriosis, P0 mice exhibited a reduced capacity to clear the infection from their spleens but not their livers whereas L0 mice had elevated bacterial titers in their livers and a modestly increased titer in their spleens. In contrast, bacterial titers in P0L0 mice were increased approximately 50- to 560-fold in their spleens and 230- to 1, 000-fold in their livers; eventual clearance of listeriae from both organs was significantly delayed. Furthermore, the resistance of P0L0 mice to secondary listeriosis was significantly reduced in their spleens and livers compared to that of WT, P0, or L0 mice. In vitro experiments indicated that immune cytotoxic T lymphocytes (CTL) lysed L. monocytogenes-infected hepatocytes primarily via a Fas-dependent, perforin-independent mechanism. The absence of Fas severely abrogated the lysis of infected hepatocytes by immune CD8(+) CTL. Taken together, these results provide the first evidence for Fas-dependent CTL-mediated lysis of L. monocytogenes-infected hepatocytes and demonstrate complementary roles for Fas and perforin in host defenses against an intracellular bacterial pathogen.

Indexed as

AnimalsCells, Culturedfas ReceptorFemaleImmunity, CellularListeria monocytogenesListeriosisLiverMaleMembrane GlycoproteinsMiceMice, Inbred C57BLMice, KnockoutPerforinPore Forming Cytotoxic ProteinsT-Lymphocytes, Cytotoxicfas ReceptorMembrane GlycoproteinsPerforinPore Forming Cytotoxic Proteins

Identifiers

PMID9712760
PMCPMC108498
OpenAlexW2160935794

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.