Evidence map›Paper›PMID 32765505›Full record

ArticleFrontiers in immunology2020

Efficient Induction of Cytotoxic T Cells by Viral Vector Vaccination Requires STING-Dependent DC Functions.

Cornelia Barnowski, Gregor Ciupka, Ronny Tao, Lei Jin, Dirk H Busch, Sha Tao, Ingo Drexler

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Viral Vector-BasedVaccines · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

7 authors at 4 institutions in 2 countries.

Cornelia BarnowskiInstitute for Virology, Düsseldorf University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.
Gregor CiupkaInstitute for Virology, Düsseldorf University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.
Ronny TaoInstitute for Virology, Düsseldorf University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.
Lei JinDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Florida, Gainesville, FL, United States.
Dirk H BuschInstitute of Microbiology, Immunology and Hygiene, Technical University Munich, Munich, Germany.
Sha TaoInstitute for Virology, Düsseldorf University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.
Ingo DrexlerInstitute for Virology, Düsseldorf University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.
Heinrich Heine University Düsseldorf · DEDüsseldorf University Hospital · DEInstitute of Medical Microbiology and Hygiene · DEUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modified Vaccinia virus Ankara (MVA) is an attenuated strain of vaccinia virus and currently under investigation as a promising vaccine vector against infectious diseases and cancer. MVA acquired mutations in host range and immunomodulatory genes, rendering the virus deficient for replication in most mammalian cells. MVA has a high safety profile and induces robust immune responses. However, the role of innate immune triggers for the induction of cytotoxic T cell responses after vaccination is incompletely understood. Stimulator of interferon genes (STING) is an adaptor protein which integrates signaling downstream of several DNA sensors and therefore mediates the induction of type I interferons and other cytokines or chemokines in response to various dsDNA viruses. Since the type I interferon response was entirely STING-dependent during MVA infection, we studied the effect of STING on primary and secondary cytotoxic T cell responses and memory T cell formation after MVA vaccination in STING KO mice. Moreover, we analyzed the impact of STING on the maturation of bone marrow-derived dendritic cells (BMDCs) and their functionality as antigen presenting cells for cytotoxic T cells during MVA infection

Indexed as

AnimalsAntigen PresentationCells, CulturedDendritic CellsFemaleGenetic VectorsHumansInterferon Type IMembrane ProteinsMiceMice, KnockoutSTING ProteinT-Lymphocytes, CytotoxicVaccinationVacciniaVaccinia virusInterferon Type IMembrane ProteinsSting1 protein, mouseSTING Proteincytotoxic T cellsdendritic cellsmodified vaccinia virus Ankara MVASTINGtype I interferonviral vector vaccine

Identifiers

PMID32765505
PMCPMC7381110
OpenAlexW3042537796

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.