Evidence map›Paper›PMID 41959667›Full record

ArticleiScience2026

Serial intravital microscopy reveals temporal dynamics of autoreactive germinal centers in the spleen.

Layla Pohl, Thomas R Wittenborn, Ali Shahrokhtash, Kristian S Kastberg, Cecilia Fahlquist-Hagert, Lisbeth Jensen, Sofie Andkær Pedersen, Julia Karen Demtröder, Donato Sardella, Alain Pulfer and 4 more

Abstract read
In one paragraph

Article in iScience, 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

14 authors.

Layla PohlDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Thomas R WittenbornDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Ali ShahrokhtashInterdisciplinary Nanoscience Center (iNANO), Aarhus University, 8000 Aarhus C, Denmark.
Kristian S KastbergDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Cecilia Fahlquist-HagertDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Lisbeth JensenDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Sofie Andkær PedersenDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Julia Karen DemtröderDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Donato SardellaDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Alain PulferInstitute for Research in Biomedicine, Faculty of Biomedical Sciences, Università della Svizzera Italiana, 6500 Bellinzona, Ticino, Switzerland.
Duncan SutherlandInterdisciplinary Nanoscience Center (iNANO), Aarhus University, 8000 Aarhus C, Denmark.
Santiago F GonzalezInstitute for Research in Biomedicine, Faculty of Biomedical Sciences, Università della Svizzera Italiana, 6500 Bellinzona, Ticino, Switzerland.
Ina Maria SchiesslDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Søren E DegnDepartment of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spleen plays a key role in clearing blood-borne infections and is involved in autoimmune and hematological disorders. It undergoes extensive remodeling during inflammation and immune reactions, but its localization in the peritoneal cavity has hampered studies of these dynamic changes. We establish a protocol for serial two-photon microscopy of the murine spleen to capture dynamic processes in the living animal over weeks. We elucidate the expansion and contraction of autoreactive germinal centers (GCs) induced by the epicutaneous application of the TLR7 agonist resiquimod. Leveraging a biocompatible abdominal imaging window, intravital labeling, and fluorescent reporters, we follow GCs for >2 weeks up to 180 μm below the capsule by tracking follicular dendritic cell networks. We also demonstrate that we can repeatedly image dynamic cell migration in the same area over a two-week period without appreciable perturbation of normal physiology, enabling a deeper understanding of the spleen and its associated disease states.

Indexed as

biological sciences research methodologiescell biologyimmunologymedical imaging

Identifiers

PMID41959667
PMCPMC13059123

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.