ReviewBioMed research international2026
Advances in Human and Animal Germinal Center Models In Vitro: New Approaches to Studying Immune Responses.
Review in BioMed research international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Germinal centers (GCs) are dynamic structures in secondary lymphoid organs where B cells undergo antigen-driven clonal selection, affinity maturation by somatic hypermutation (SHM), and class switch recombination (CSR), resulting in the generation of high-affinity antigen-specific long-lived plasma cells and memory B cells. Reconstructing these processes in vitro is critical for mechanistic studies and for advancing translational applications in vaccinology and immunotherapy. This review examines human and murine approaches to in vitro models of GC-like reactions, including conventional cultures, three-dimensional (3D) scaffolds, organoids, and microfluidic systems. We summarize the stimuli and culture conditions used across studies, highlighting common requirements, as well as model-specific strategies. Most models effectively induced B cell proliferation, CSR, and plasma cell differentiation. In contrast, SHM and clonal selection, key features of the GC, were less frequently shown, reflecting the technical complexity of reproducing these events in vitro. Finally, we outline the main challenges in recreating a fully functional GC and suggest future directions for refining these models to more closely mimic the secondary lymphoid organ environment.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.