Evidence map›Paper›PMID 36504430›Full record

ArticleClinical and translational medicine2022

Differential expression of CD8 defines phenotypically distinct cytotoxic T cells in cancer and multiple sclerosis.

Tobias Burkard, Martina Herrero San Juan, Caroline Dreis, Anastasiia Kiprina, Dmitry Namgaladze, Kai Siebenbrodt, Sebastian Luger, Christian Foerch, Josef M Pfeilschifter, Andreas Weigert and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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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

11 authors at 1 institution in 1 country.

Tobias BurkardPharmazentrum Frankfurt/ZAFES, Institute of Pharmacology and Toxicology, Hospital of the Goethe University, Frankfurt am Main, Germany.
Martina Herrero San JuanPharmazentrum Frankfurt/ZAFES, Institute of Pharmacology and Toxicology, Hospital of the Goethe University, Frankfurt am Main, Germany.
Caroline DreisPharmazentrum Frankfurt/ZAFES, Institute of Pharmacology and Toxicology, Hospital of the Goethe University, Frankfurt am Main, Germany.
Anastasiia KiprinaFaculty of Medicine, Institute of Biochemistry I, Goethe-University Frankfurt/Main, Frankfurt am Main, Germany.
Dmitry NamgaladzeFaculty of Medicine, Institute of Biochemistry I, Goethe-University Frankfurt/Main, Frankfurt am Main, Germany.
Kai SiebenbrodtDepartment of Neurology, Goethe University Hospital Frankfurt, Frankfurt am Main, Germany.
Sebastian LugerDepartment of Neurology, Goethe University Hospital Frankfurt, Frankfurt am Main, Germany.
Christian FoerchDepartment of Neurology, Goethe University Hospital Frankfurt, Frankfurt am Main, Germany.
Josef M PfeilschifterPharmazentrum Frankfurt/ZAFES, Institute of Pharmacology and Toxicology, Hospital of the Goethe University, Frankfurt am Main, Germany.
Andreas WeigertFaculty of Medicine, Institute of Biochemistry I, Goethe-University Frankfurt/Main, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0002-7529-1952
Heinfried H RadekePharmazentrum Frankfurt/ZAFES, Institute of Pharmacology and Toxicology, Hospital of the Goethe University, Frankfurt am Main, Germany.
Goethe University Frankfurt · DE

Funding

Deutsche Forschungsgemeinschaft B04Deutsche Forschungsgemeinschaft B06Deutsche Forschungsgemeinschaft GRK2336Deutsche Forschungsgemeinschaft SFB1039Deutsche Forschungsgemeinschaft TP01
6 · The paper itself

Abstract

backgroundCytotoxic T lymphocytes take on a leading role in many immune-related diseases. They function as key effector immune cells fighting cancer cells, but they are also considerably involved in autoimmune diseases. Common to both situations, CD8

methodsWe used an in vitro starvation as well as rapamycin treatment protocol mimicking nutrient deprivation to generate CD8

resultsStarvation induced a decreased expression of CD8, yielding a CD8

conclusionsIn summary, our data show that functionally distinct cytotoxic T lymphocytes can be identified based on their expression of CD8. Indicating a more general role in CD8 T cell immunity, these cells may play opposing roles in the TME, and also in the pathophysiology of autoimmune diseases such as multiple sclerosis.

Indexed as

Autoimmune DiseasesMultiple SclerosisCD8-Positive T-LymphocytesHumansNeoplasm Recurrence, LocalT-Lymphocytes, CytotoxicTumor MicroenvironmentCD8+ T cellsmTORmultiple sclerosismultispectral imagingtumour immunity

Identifiers

PMID36504430
PMCPMC9742381
OpenAlexW4311127083

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.