Evidence map›Paper›PMID 31916677›Full record

ArticleEMBO molecular medicine2020

"Designer cytokines" targeting the tumor vasculature-think global and act local.

Thomas Kammertoens, Josephine Kemna, Matthias Leisegang

Open access · goldAbstract readComment
In one paragraph

Article in EMBO molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 58% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. CD4Science (New York, N.Y.) · 2026
    Article
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Thomas KammertoensInstitute of Immunology, Charité-Universitätsmedizin Berlin, Campus Buch, Berlin, Germany.ORCID 0000-0003-3309-5141
Josephine KemnaMax-Delbrück-Center for Molecular Medicine, Berlin, Germany.ORCID 0000-0002-2172-4441
Matthias LeisegangInstitute of Immunology, Charité-Universitätsmedizin Berlin, Campus Buch, Berlin, Germany.ORCID 0000-0003-3692-7142
Charité - Universitätsmedizin Berlin · DEMax Delbrück Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor (TNF) was discovered in 1975 as a lipopolysaccharide-induced serum factor that causes necrosis of tumors (Carswell et al, 1975). It was later found that TNF and cachectin, a factor causing wasting disease, were one and the same molecule (Beutler et al, 1985). Studies on the inflammatory activity of TNF have been translated into clinical success, namely blocking antibodies used to suppress autoimmune diseases. Research on TNF anti-tumor activity, in contrast, has not yet resulted in a therapeutic breakthrough. This may change, based on a study by Huyghe et al (2020) describing novel "designer cytokines" (TNF and interferon-γ) that increase local activity by targeting the CD13-positive tumor vasculature, while simultaneously lowering the binding affinity to the respective cytokine receptor, thereby reducing off-target effects on normal cells.

Indexed as

CytokinesTumor Necrosis Factor-alphaImmunotherapyInterferon-gammaLipopolysaccharidesCytokinesInterferon-gammaLipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID31916677
PMCPMC7005528
OpenAlexW3000433841

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.