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The liver contains distinct interconnected networks of CX3CR1 + macrophages, XCR1 + type 1 and CD301a + type 2 conventional dendritic cells embedded within portal tracts

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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cphy.c120018openalex-snapshot
Hepatic Nervous System and Neurobiology of the Liver
inferredcites →https://doi.org/10.1002/dvg.20335openalex-snapshot
A global double‐fluorescent Cre reporter mouse
inferredcites →https://doi.org/10.1002/hep.1840150403openalex-snapshot
The Histological Features of Chronic Hepatitis C and Autoimmune Chronic Hepatitis: A Comparative Analysis
inferredcites →https://doi.org/10.1002/hep.1840220203openalex-snapshot
Focal lymphocytic aggregates in chronic hepatitis C: Occurrence, immunohistochemical characterization, and relation to markers of autoimmunity
inferredcites →https://doi.org/10.1002/hep.29494openalex-snapshot
Viral persistence, liver disease, and host response in a hepatitis C–like virus rat model
inferredcites →https://doi.org/10.1016/0022-1759(82)90035-7openalex-snapshot
Fading of immunofluorescence during microscopy: a study of the phenomenon and its remedy
inferredcites →https://doi.org/10.1016/j.cell.2015.08.004openalex-snapshot
Robust Anti-viral Immunity Requires Multiple Distinct T Cell-Dendritic Cell Interactions
inferredcites →https://doi.org/10.1016/j.cell.2019.09.035openalex-snapshot
Transcriptional Basis of Mouse and Human Dendritic Cell Heterogeneity
inferredcites →https://doi.org/10.1016/j.cell.2021.12.018openalex-snapshot
Spatial proteogenomics reveals distinct and evolutionarily conserved hepatic macrophage niches
inferredcites →https://doi.org/10.1016/j.immuni.2015.07.020openalex-snapshot
Spatiotemporally Distinct Interactions with Dendritic Cell Subsets Facilitates CD4+ and CD8+ T Cell Activation to Localized Viral Infection
inferredcites →https://doi.org/10.1016/j.immuni.2017.07.018openalex-snapshot
A Liver Capsular Network of Monocyte-Derived Macrophages Restricts Hepatic Dissemination of Intraperitoneal Bacteria by Neutrophil Recruitment
inferredcites →https://doi.org/10.1016/j.immuni.2020.04.005openalex-snapshot
Inflammatory Type 2 cDCs Acquire Features of cDC1s and Macrophages to Orchestrate Immunity to Respiratory Virus Infection
inferredcites →https://doi.org/10.1016/s0002-9440(10)63141-0openalex-snapshot
Interleukin-10 Secretion Differentiates Dendritic Cells from Human Liver and Skin
inferredcites →https://doi.org/10.1038/s41577-018-0088-1openalex-snapshot
Dendritic cell subsets in T cell programming: location dictates function
inferredcites →https://doi.org/10.1038/s41577-020-00413-xopenalex-snapshot
Genetic models of human and mouse dendritic cell development and function
inferredcites →https://doi.org/10.1038/s41586-019-1620-6openalex-snapshot
Dynamics and genomic landscape of CD8+ T cells undergoing hepatic priming
inferredcites →https://doi.org/10.1038/s41586-020-2611-3openalex-snapshot
cDC1 prime and are licensed by CD4+ T cells to induce anti-tumour immunity
inferredcites →https://doi.org/10.1038/s41586-020-2977-2openalex-snapshot
Commensal-driven immune zonation of the liver promotes host defence
inferredcites →https://doi.org/10.1038/s41591-021-01344-3openalex-snapshot
XCR1+ type 1 conventional dendritic cells drive liver pathology in non-alcoholic steatohepatitis
inferredcites →https://doi.org/10.1073/pnas.1708981114openalex-snapshot
Multiplex, quantitative cellular analysis in large tissue volumes with clearing-enhanced 3D microscopy (C e 3D)
inferredcites →https://doi.org/10.1073/pnas.96.13.7324openalex-snapshot
Normal growth and development in the absence of hepatic insulin-like growth factor I
inferredcites →https://doi.org/10.1084/jem.149.1.1openalex-snapshot
Identification of a novel cell type in peripheral lymphoid organs of mice. V. Purification of spleen dendritic cells, new surface markers, and maintenance in vitro.
inferredcites →https://doi.org/10.1097/00007890-198408000-00016openalex-snapshot
PHENOTYPE AND HISTOLOGICAL DISTRIBUTION OF INTERSTITIAL DENDRITIC CELLS IN THE RAT PANCREAS, LIVER, HEART, AND KIDNEY
inferredcites →https://doi.org/10.1097/00007890-198811000-00024openalex-snapshot
CHARACTERIZATION OF INTERSTITIAL DENDRITIC CELLS IN HUMAN LIVER
inferredcites →https://doi.org/10.1111/imcb.12476openalex-snapshot
Zone defence – the gut microbiota position macrophages for optimal liver protection
inferredcites →https://doi.org/10.1126/science.aal1962openalex-snapshot
Mouse models of acute and chronic hepacivirus infection
inferredcites →https://doi.org/10.1126/science.aau0964openalex-snapshot
Two distinct interstitial macrophage populations coexist across tissues in specific subtissular niches
inferredcites →https://doi.org/10.1128/mcb.20.11.4106-4114.2000openalex-snapshot
Analysis of Fractalkine Receptor CX3CR1 Function by Targeted Deletion and Green Fluorescent Protein Reporter Gene Insertion
inferredcites →https://doi.org/10.1182/blood-2008-05-159921openalex-snapshot
Hepatic microenvironment programs hematopoietic progenitor differentiation into regulatory dendritic cells, maintaining liver tolerance
inferredcites →https://doi.org/10.1182/blood-2010-02-266296openalex-snapshot
An antibody against the colony-stimulating factor 1 receptor depletes the resident subset of monocytes and tissue- and tumor-associated macrophages but does not inhibit inflammation
inferredcites →https://doi.org/10.1186/1471-2164-14-669openalex-snapshot
Gut microbiota dysbiosis and bacterial community assembly associated with cholesterol gallstones in large-scale study
inferredcites →https://doi.org/10.4049/jimmunol.1202798openalex-snapshot
Critical Roles of a Dendritic Cell Subset Expressing a Chemokine Receptor, XCR1
inferredcites →https://doi.org/10.4049/jimmunol.1402622openalex-snapshot
Liver-Resident CD103+ Dendritic Cells Prime Antiviral CD8+ T Cells In Situ
inferredcites →https://doi.org/10.4049/jimmunol.164.6.2978openalex-snapshot
CD4 and CD8 Expression by Dendritic Cell Subtypes in Mouse Thymus and Spleen
inferredcites →https://doi.org/10.4049/jimmunol.172.2.1009openalex-snapshot
Liver Dendritic Cells Are Less Immunogenic Than Spleen Dendritic Cells because of Differences in Subtype Composition
inferredcites →https://doi.org/10.4049/jimmunol.176.4.2161openalex-snapshot
A Major Lung CD103 (αE)-β7 Integrin-Positive Epithelial Dendritic Cell Population Expressing Langerin and Tight Junction Proteins

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4775199openalex-extracted
Visualizing the Spatial Organization of Monocytes, Connective and Tissue Specific Macrophages in situ
inferred← citeshttps://doi.org/10.1002/eji.202149641openalex-snapshot
The “Domino effect” in MASLD: The inflammatory cascade of steatohepatitis
inferred← citeshttps://doi.org/10.1016/b978-0-128-24465-4.00085-5openalex-snapshot
Microanatomy and Immunity in the Liver
inferred← citeshttps://doi.org/10.1016/j.arr.2026.103039openalex-snapshot
Ageing and liver immune cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114847openalex-snapshot
Visualizing the spatial organization of monocytes, interstitial macrophages, and tissue-specific macrophages in situ
inferred← citeshttps://doi.org/10.1021/acs.analchem.4c00228openalex-snapshot
Multicolor Two-Photon Microscopy Imaging of Lipid Droplets and Liver Capsule Macrophages In Vivo
inferred← citeshttps://doi.org/10.1038/s41423-025-01324-4openalex-snapshot
Myeloid cells in chronic liver inflammation
inferred← citeshttps://doi.org/10.1038/s41467-024-45612-5openalex-snapshot
A hepatic network of dendritic cells mediates CD4 T cell help outside lymphoid organs
inferred← citeshttps://doi.org/10.1038/s41467-026-71537-2openalex-snapshot
An immunobiliary single-cell atlas resolves crosstalk between type 2 conventional dendritic cells and γδ T cells in cholangitis
inferred← citeshttps://doi.org/10.1038/s41586-024-07372-6openalex-snapshot
Periportal macrophages protect against commensal-driven liver inflammation
inferred← citeshttps://doi.org/10.1038/s41590-025-02150-6openalex-snapshot
Intestinal neuron-associated macrophages in health and disease
inferred← citeshttps://doi.org/10.1038/s41590-025-02199-3openalex-snapshot
CD4+ T cells license Kupffer cells to reverse CD8+ T cell dysfunction induced by hepatocellular priming
inferred← citeshttps://doi.org/10.1038/s44319-025-00580-9openalex-snapshot
A comprehensive molecular atlas of the mesenchymal cell types in the mouse liver
inferred← citeshttps://doi.org/10.1101/2025.01.24.634721openalex-snapshot
A comprehensive molecular atlas of the cell types in the mouse liver
inferred← citeshttps://doi.org/10.1101/2025.07.10.664083openalex-snapshot
An immunobiliary single-cell atlas resolves crosstalk of type 2 cDCs and γδT cells in cholangitis
inferred← citeshttps://doi.org/10.1111/imcb.12612openalex-snapshot
Immunology & Cell Biology's Top 10 original research articles 2021–2022
inferred← citeshttps://doi.org/10.1126/sciadv.adh0831openalex-snapshot
Therapeutic blockade of ER stress and inflammation prevents NASH and progression to HCC
inferred← citeshttps://doi.org/10.1146/annurev-immunol-090122-041354openalex-snapshot
Priming and Maintenance of Adaptive Immunity in the Liver
inferred← citeshttps://doi.org/10.1177/03009858251352581openalex-snapshot
Immunohistochemical characterization of cells of the mononuclear phagocyte system in the mouse
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1379225openalex-snapshot
The role of dendritic cells in MASH: friends or foes?
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1763348openalex-snapshot
CX3CL1/CX3CR1 axis in liver disease: context-dependent roles and balance
inferred← citeshttps://doi.org/10.3390/ijms25179331openalex-snapshot
Mechanisms of Tolerance Induction in Liver Transplantation: Lessons Learned from Fetomaternal Tolerance, Autoimmunity and Tumor Immunity
inferred← citeshttps://doi.org/10.70675/8248c540zb671z4690z9d3dz2b77ffb9a4bbopenalex-snapshot
La réplication du virus de l'hépatite B et son échappement à la réponse immunitaire sont favorisés par l'expression de l'ARNsp1, codant pour les protéines HBSP et HBc-Cys
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