Evidence map›Paper›PMID 34885056›Full record

ReviewCancers2021

The Serine Protease CD26/DPP4 in Non-Transformed and Malignant T Cells.

Guranda Chitadze, Ulrike Wehkamp, Ottmar Janssen, Monika Brüggemann, Marcus Lettau

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Bone Loss in Diabetes Mellitus: Diaporosis.International journal of molecular sciences · 2024
    Review
  6. Review
  7. Review
  8. Depletion of polyfunctional CD26Experimental hematology & oncology · 2023
    Article
  9. CD26 and Cancer.Cancers · 2022
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. 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 2 institutions in 1 country.

Guranda ChitadzeUnit for Hematological Diagnostics, Department of Internal Medicine II, University Hospital Schleswig-Holstein, Langer Segen 8-10, D-24105 Kiel, Germany.
Ulrike WehkampDepartment of Dermatology, University Hospital Schleswig-Holstein, Arnold-Heller-Str. 3, Bldg. C, D-24105 Kiel, Germany.
Ottmar JanssenInstitute of Immunology, University Hospital Schleswig-Holstein, Christian-Albrechts University Kiel, Arnold-Heller-Str. 3, Bldg. U30, D-24105 Kiel, Germany.ORCID 0000-0002-9612-8900
Monika BrüggemannUnit for Hematological Diagnostics, Department of Internal Medicine II, University Hospital Schleswig-Holstein, Langer Segen 8-10, D-24105 Kiel, Germany.
Marcus LettauUnit for Hematological Diagnostics, Department of Internal Medicine II, University Hospital Schleswig-Holstein, Langer Segen 8-10, D-24105 Kiel, Germany.ORCID 0000-0002-3824-9923
University Hospital Schleswig-Holstein · DEChristian-Albrechts-Universität zu Kiel · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD26/Dipeptidylpeptidase 4 is a transmembrane serine protease that cleaves off N-terminal dipeptides. CD26/DPP4 is expressed on several immune cell types including T and NK cells, dendritic cells, and activated B cells. A catalytically active soluble form of CD26/DPP4 can be released from the plasma membrane. Given its wide array of substrates and interaction partners CD26/DPP4 has been implicated in numerous biological processes and effects can be dependent or independent of its enzymatic activity and are exerted by the transmembrane protein and/or the soluble form. CD26/DPP4 has been implicated in the modulation of T-cell activation and proliferation and CD26/DPP4-positive T cells are characterized by remarkable anti-tumor properties rendering them interesting candidates for T cell-based immunotherapies. Moreover, especially in cutaneous T-cell lymphoma CD26/DPP4 expression patterns emerged as an established marker for diagnosis and treatment monitoring. Surprisingly, besides a profound knowledge on substrates, interaction partners, and associated signal transduction pathways, the precise role of CD26/DPP4 for T cell-based immune responses is only partially understood.

Indexed as

CD26cutaneous T-cell lymphomacytotoxic granulesdipeptidyl peptidase 4DPP4mycosis fungoidesSézary syndromeT cells

Identifiers

PMID34885056
PMCPMC8657226
OpenAlexW3215018281

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.