Evidence map›Paper›PMID 32639988›Full record

ArticlePloS one2020

Placenta-specific 8 limits IFNγ production by CD4 T cells in vitro and promotes establishment of influenza-specific CD8 T cells in vivo.

Chris D Slade, Katie L Reagin, Hari G Lakshmanan, Kimberly D Klonowski, Wendy T Watford

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. 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
1.4field-weighted citation impact, top 19% 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, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Multifaced roles of PLAC8 in cancer.Biomarker research · 2021
    Review
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.

Chris D SladeDepartment of Infectious Diseases, University of Georgia, Athens, GA, United States of America.
Katie L ReaginDepartment of Cellular Biology, University of Georgia, Athens, GA, United States of America.
Hari G LakshmananDepartment of Cellular Biology, University of Georgia, Athens, GA, United States of America.
Kimberly D KlonowskiDepartment of Infectious Diseases, University of Georgia, Athens, GA, United States of America.
Wendy T WatfordDepartment of Infectious Diseases, University of Georgia, Athens, GA, United States of America.ORCID 0000-0003-4261-5399
University of Georgia · US

Funding

Defining the mechanisms by which Placenta-specific 8 (Plac8) facilitates CD8 memory formationR21AI138027 · NIAID · UNIVERSITY OF GEORGIA · PI KLONOWSKI, KIMBERLY D., WATFORD, WENDY T · 2019 to 2020
$414k
NIAID NIH HHS R21 AI138027
6 · The paper itself

Abstract

During type 1 immune responses, CD4 T helper 1 (Th1) cells and CD8 T cells are activated via IL-12 and contribute to the elimination of intracellular pathogens through interferon gamma (IFNγ) production. In this study, we identified Placenta-specific 8 (Plac8) as a gene that is uniquely expressed in Th1 CD4 T cells relative to other CD4 T cell subsets and hypothesized that Plac8 may represent a novel therapeutic target in Th1 CD4 T cells. First, we determined that Plac8 mRNA in CD4 T cells was induced following IL-12 stimulation via an indirect route that required new protein synthesis. Upon evaluating the functional relevance of Plac8 expression in Th1 CD4 T cells, we discovered that Plac8 was important for suppressing IFNγ mRNA and protein production by CD4 T cells 24 hours after IL-12 stimulation, however Plac8 did not contribute to pathogenic CD4 T cell function during two models of intestinal inflammation. We also noted relatively high basal expression of Plac8 in CD8 T cells which could be further induced following IL-12 stimulation in CD8 T cells. Furthermore, Plac8 expression was important for establishing an optimal CD8 T cell response against influenza A virus via a T cell-intrinsic manner. Altogether, these results implicate Plac8 as a potential regulator of Th1 CD4 and CD8 T cell responses during Th1 T cell-driven inflammation.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesColitisDisease Models, AnimalInterferon-gammaInterleukin-12Leukocyte Common AntigensMiceMice, Inbred C57BLMice, KnockoutOrthomyxoviridae InfectionsProteinsRNA, MessengerUp-RegulationInterferon-gammaInterleukin-12Leukocyte Common AntigensPlac8 protein, mouseProteinsPtprc protein, mouseRNA, Messenger

Identifiers

PMID32639988
PMCPMC7343148
OpenAlexW3041245012

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.