Evidence map›Paper›PMID 34680356›Full record

ArticleCancers2021

Landscape of 4D Cell Interaction in Hodgkin and Non-Hodgkin Lymphomas.

Sylvia Hartmann, Sonja Scharf, Yvonne Steiner, Andreas G Loth, Emmanuel Donnadieu, Nadine Flinner, Viola Poeschel, Stephanie Angel, Moritz Bewarder, Julia Bein and 7 more

Open access · goldAbstract read
In one paragraph

Article 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
2.3field-weighted citation impact, top 12% 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, 19 citations in OpenAlex.

  1. Review
  2. [Diffuse large B-cell lymphoma and Hodgkin lymphoma].Pathologie (Heidelberg, Germany) · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Imaging bridges pathology and radiology.Journal of pathology informatics · 2023
    Review
  13. 3D analyses reveal T cells with activated nuclear features in T-cell/histiocyte-rich large B-cell lymphoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  14. Article
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

17 authors at 4 institutions in 2 countries.

Sylvia HartmannDr. Senckenberg Institute of Pathology, Goethe University Frankfurt am Main, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.ORCID 0000-0003-3424-1091
Sonja ScharfFrankfurt Institute of Advanced Studies, 60438 Frankfurt am Main, Germany.ORCID 0000-0002-0300-7027
Yvonne SteinerDr. Senckenberg Institute of Pathology, Goethe University Frankfurt am Main, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
Andreas G LothDepartment of Otolaryngology, Head and Neck Surgery, University Hospital Frankfurt, 60590 Frankfurt am Main, Germany.ORCID 0000-0001-5221-6565
Emmanuel DonnadieuInstitut Cochin, INSERM U1016/CNRS UMR 8104, Université de Paris, 75014 Paris, France.ORCID 0000-0002-4985-7254
Nadine FlinnerDr. Senckenberg Institute of Pathology, Goethe University Frankfurt am Main, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
Viola PoeschelInternal Medicine I, Saarland University Medical School, 66421 Homburg, Germany.
Stephanie AngelInternal Medicine I, Saarland University Medical School, 66421 Homburg, Germany.
Moritz BewarderInternal Medicine I, Saarland University Medical School, 66421 Homburg, Germany.
Julia BeinDr. Senckenberg Institute of Pathology, Goethe University Frankfurt am Main, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
Uta BrunnbergDepartment of Internal Medicine 2, Goethe University Hospital, 60590 Frankfurt am Main, Germany.
Alessandro BozzatoDepartment of Otorhinolaryngology, Head and Neck Surgery, Saarland University Medical Center, 66421 Homburg, Germany.ORCID 0000-0002-9648-8834
Bernhard SchickDepartment of Otorhinolaryngology, Head and Neck Surgery, Saarland University Medical Center, 66421 Homburg, Germany.
Stephan StilgenbauerInternal Medicine I, Saarland University Medical School, 66421 Homburg, Germany.
Rainer M BohleInstitute of Pathology, Saarland University Medical School, 66421 Homburg, Germany.
Lorenz ThurnerInternal Medicine I, Saarland University Medical School, 66421 Homburg, Germany.
Martin-Leo HansmannFrankfurt Institute of Advanced Studies, 60438 Frankfurt am Main, Germany.
Goethe University Frankfurt · DESaarland University · DECentre National de la Recherche Scientifique · FRUniversity Hospital Ulm · DE

Funding

BMBF COMPLS2-087-Patho234Deutsche Forschungsgemeinschaft HA6145/2-1 and HA6145/6-1
6 · The paper itself

Abstract

Profound knowledge exists about the clinical, morphologic, genomic, and transcriptomic characteristics of most lymphoma entities. However, information is currently lacking on the dynamic behavior of malignant lymphomas. This pilot study aimed to gain insight into the motility of malignant lymphomas and bystander cells in 20 human lymph nodes. Generally, B cells were faster under reactive conditions compared with B cells in malignant lymphomas. In contrast, PD1-positive T cells did not show systematic differences in velocity between reactive and neoplastic conditions in general. However, lymphomas could be divided into two groups: one with fast PD1-positive T cells (e.g., Hodgkin lymphoma and mantle cell lymphoma; means 8.4 and 7.8 µm/min) and another with slower PD1-positive T cells (e.g., mediastinal grey zone lymphoma; mean 3.5 µm/min). Although the number of contacts between lymphoma cells and PD1-positive T cells was similar in different lymphoma types, important differences were observed in the duration of these contacts. Among the lymphomas with fast PD1-positive T cells, contacts were particularly short in mantle cell lymphoma (mean 54 s), whereas nodular lymphocyte-predominant Hodgkin lymphoma presented prolonged contact times (mean 6.1 min). Short contact times in mantle cell lymphoma were associated with the largest spatial displacement of PD1-positive cells (mean 12.3 µm). Although PD1-positive T cells in nodular lymphocyte-predominant Hodgkin lymphoma were fast, they remained in close contact with the lymphoma cells, in line with a dynamic immunological synapse. This pilot study shows for the first time systematic differences in the dynamic behavior of lymphoma and bystander cells between different lymphoma types.

Indexed as

cell contactscell motilityHodgkin lymphomamigrationnon-Hodgkin lymphoma

Identifiers

PMID34680356
PMCPMC8534096
OpenAlexW3207284080

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.