ReviewImmunological reviews2026
Dendritic Cell Organization and Function in Innate and Adaptive Immune Defense Within Lymph Nodes.
Review in Immunological reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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
2 citing papers in PubMed.
- 25 Years of Cancer Immunoediting: Dendritic Cells and Macrophages Filled the Missing Gap.Cancers · 2026Review
- Beyond BMI: visceral adiposity assessed by the lipid accumulation product index shows independent associations with IL-5 and TNF-β in older adults.Aging clinical and experimental research · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Lymph nodes (LNs) are highly organized secondary lymphoid organs that serve as critical hubs for immune defense. They filter lymph and enable efficient immune surveillance, elicit potent innate responses to prevent systemic pathogen spread, and generate adaptive immunity for long-lived protection. It has now been established that conventional dendritic cells (DCs), canonically recognized as professional antigen-presenting cells that instruct T cell responses, play foundational roles in coordinating all these functions of the LN. DCs are the most abundant innate cell type in the LN parenchyma, and their ability to mediate these processes is intimately tied to their spatial organization. Rather than being randomly dispersed, different DC subsets preferentially occupy distinct niches within the tissue. This positioning regulates their homeostatic maintenance, access to different types of antigens, and interactions with other immune cells, which collectively shape the ensuing immune response. In this review, we summarize the current understanding of how the spatiotemporal dynamics and functional cooperation of DC subsets, and other innate populations, underpin diverse immunological functions of the LN, ranging from steady-state surveillance to the development of synchronized and tailored innate and adaptive responses to pathogens or following vaccination.
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Registered trials
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