Evidence map›Paper›PMID 42707683›Full record

ReviewFrontiers in immunology2026

The 3D landscape of infection: spatial organization and

Oliver Goldmann, Eva Medina

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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

2 authors.

Oliver GoldmannInfection Immunology Research Group, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Eva MedinaInfection Immunology Research Group, Helmholtz Centre for Infection Research, Braunschweig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbial infections rarely consist of free-floating cells. Instead, pathogens and immune cells are typically organized into complex three-dimensional (3D) structures, including biofilms, abscesses, and granulomas, which can serve to constrain pathogen dissemination. At the same time, these architectures create protective microenvironments that promote microbial persistence, immune evasion, and increased resistance to antimicrobial therapies. A mechanistic understanding of how spatially organized tissue structures and local microenvironmental cues shape host-pathogen dynamics may open new avenues for therapeutic interventions, for example by improving targeted drug delivery, enhancing antibiotic penetration, or disrupting protective microbial niches. In this review, we summarize emerging insights into the 3D landscape of infections and highlight advances in experimental platforms that more faithfully recapitulate tissue architecture, including 3D cell culture systems, bioprinted tissue, organoids, and organ-on-chip technologies. Finally, we discuss how integrating spatial parameters into infection models reshapes our understanding of pathogenesis and opens new conceptual and therapeutic avenues for combating infections.

Indexed as

InfectionsAbscessAnimalsBiofilmsBioprintingCell Culture Techniques, Three DimensionalCellular MicroenvironmentGranulomaHost-Pathogen InteractionsHumansMicrophysiological SystemsModels, BiologicalOrganoidsabscessbiofilmbioprintingbioreactorgranulomaorganoidsorgan-on-chipspheroids

Identifiers

PMID42707683
PMCPMC13548045

What OpenQuestion holds

Textmetadata
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.