Evidence map›Paper›PMID 41686816›Full record

ArticlePLOS digital health2026

The three-dimensional landscape of tumor-associated macrophages in reactive and neoplastic human lymph nodes.

Aleksandar Vladisavljevic, Sonja Scharf, Hendrik Schäfer, Jörg Ackermann, Sylvia Hartmann, Ina Koch, Martin-Leo Hansmann, Patrick Wurzel

Abstract read
In one paragraph

Article in PLOS digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Aleksandar VladisavljevicInstitute of General Pharmacology and Toxicology, Goethe-University Frankfurt, Frankfurt, Germany.ORCID https://orcid.org/0009-0008-7868-9158
Sonja ScharfInstitute of General Pharmacology and Toxicology, Goethe-University Frankfurt, Frankfurt, Germany.ORCID https://orcid.org/0000-0002-0300-7027
Hendrik SchäferInstitute of General Pharmacology and Toxicology, Goethe-University Frankfurt, Frankfurt, Germany.ORCID https://orcid.org/0000-0002-5859-250X
Jörg AckermannMolecular Bioinformatics, Goethe-University Frankfurt, Frankfurt, Germany.
Sylvia HartmannDr. Senckenberg Institute of Pathology, Goethe-University Frankfurt, Frankfurt, Germany.
Ina KochMolecular Bioinformatics, Goethe-University Frankfurt, Frankfurt, Germany.
Martin-Leo HansmannInstitute of General Pharmacology and Toxicology, Goethe-University Frankfurt, Frankfurt, Germany.
Patrick WurzelInstitute of General Pharmacology and Toxicology, Goethe-University Frankfurt, Frankfurt, Germany.ORCID https://orcid.org/0000-0002-2366-9124

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages play a crucial role in the homeostasis of lymph nodes. Their phenotypes and functions are dictated by the molecular composition of the microenvironment. The presence of tumor cells can influence the microenvironment, leading to changes in the cellular functions of tumor-associated macrophages (TAMs). Cellular alterations often correlate with histomorphometric and distributional changes. This study aims to characterize these pathomic modifications resulting from tumor cell infiltration by comparing them to reactive conditions. We assessed CD68+ and CD163+ TAMs in 160 three-dimensional (3D) images of human lymphoid tissue sections derived from 82 cases comprising six different diagnoses. To investigate TAM profiles, we employed a hybrid approach involving computer vision and graph theoretical algorithms. For calculating the histomorphometric features of TAMs, we utilized an image analysis pipeline with IMARIS Advanced Tracking Software. The distributions of TAMs were characterized using cell graphs. The incorporation of 3D tissue analysis in targeted areas of thick tissue sections revealed specific patterns of histomorphometric and distributional changes in TAMs. In chronic lymphocytic leukemia and diffuse large B-cell lymphoma, these distinctive alteration patterns demonstrated entity specificity. Furthermore, pathomic alterations displayed possible correlations with established functional aberrations in lymphomas. These findings imply that the pathomic properties of TAMs mirror their functional aberrations. Through validation and generalization via molecular pathological examinations, this approach has the potential to unveil and understand functional aberrations in histopathological assessments.

Identifiers

PMID41686816
PMCPMC12904395

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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.