Evidence map›Paper›PMID 41988691›Full record

ArticleAdvanced healthcare materials2026

Enhanced Human Antigen-Specific B Cell Responses Using In Vitro 3D Tonsil Cultures Containing Stromal Cells.

Maaike V J Braham, Marlon de Gast, Liubov Babii, Sabine Kruijer, Theo M Bestebroer, Mathilde Richard, Mathieu Claireaux, S Marieke van Ham, Jelle de Wit, Cécile A C M van Els and 2 more

Abstract read
In one paragraph

Article in Advanced healthcare materials, 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

12 authors.

Maaike V J BrahamSanquin, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-0235-0632
Marlon de GastAmsterdam Institute for Immunology and Infectious Diseases, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-3976-8183
Liubov BabiiSanquin, Amsterdam, The Netherlands.
Sabine KruijerAmsterdam Institute for Immunology and Infectious Diseases, Amsterdam, The Netherlands.
Theo M BestebroerDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.
Mathilde RichardDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0003-0240-9312
Mathieu ClaireauxAmsterdam Institute for Immunology and Infectious Diseases, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-1890-9493
S Marieke van HamSanquin, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-1999-9494
Jelle de WitCentre For Immunology of Infectious Diseases and Vaccines, Department of Immune Mechanisms, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID https://orcid.org/0000-0003-2444-6050
Cécile A C M van ElsCentre For Immunology of Infectious Diseases and Vaccines, Department of Immune Mechanisms, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.ORCID https://orcid.org/0000-0003-1995-8641
Anja Ten BrinkeSanquin, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-0135-7496
Marit J van GilsAmsterdam Institute for Immunology and Infectious Diseases, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-3422-8161

Funding

Amsterdam University Medical Centers Fellowship2027Netherlands Organization for Scientific Research Aspasia-015.014.070Netherlands Organization for Scientific Research OCENW.KLEIN.479
6 · The paper itself

Abstract

Germinal centers (GCs) are specialized sites within secondary lymphoid organs where B cells expand, are selected, and mature to produce high-quality antibodies. Their structural complexity makes them difficult to model in vitro. Here, we developed a human 3D lymphoid culture system combining lymphoid and stromal cells to better mimic GC environments than conventional 2D cultures. Tonsil cells were cultured with or without fibroblastic reticular cells (FRCs) in 2D or 3D hydrogels and stimulated with viral antigens or vaccines. FRC-supported 3D cultures significantly improved B and T cell survival and promoted reaggregation into follicle-like structures with. 3D FRC-supported co-cultures higher levels of antigen-specific antibodies, increased frequencies of S- or HA-specific B cells, and enhanced differentiation into antibody-secreting cells. Importantly, these cultures also showed reduced cell death and lower bystander activation and CXCR4 and CXCR5 expression on CD27

Indexed as

AntigensB-LymphocytesCell Culture Techniques, Three DimensionalPalatine TonsilStromal CellsCell Culture TechniquesCell DifferentiationCells, CulturedCoculture TechniquesGerminal CenterHumansT-LymphocytesAntigens3D culture systemantibody‐secreting cellsfibroblastic reticular cellsgerminal center responsehydrogelorganoidvaccine

Identifiers

PMID41988691
PMCPMC13279853

What OpenQuestion holds

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Registered trials

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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.