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Exosomes loading Tapasin enhance T cell immune response by autophagy to inhibit HBV replication

https://doi.org/10.1002/jmv.28746
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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/jum.14898openalex-snapshot
Exosomes Derived From Low‐Intensity Pulsed Ultrasound‐Treated Dendritic Cells Suppress Tumor Necrosis Factor–Induced Endothelial Inflammation
inferredcites →https://doi.org/10.1007/s00253-019-10257-8openalex-snapshot
Targeting PI3K/AKT/mTOR-mediated autophagy for tumor therapy
inferredcites →https://doi.org/10.1016/j.antiviral.2012.07.011openalex-snapshot
Strong and multi-antigen specific immunity by hepatitis B core antigen (HBcAg)-based vaccines in a murine model of chronic hepatitis B: HBcAg is a candidate for a therapeutic vaccine against hepatitis B virus
inferredcites →https://doi.org/10.1016/j.coi.2018.04.014openalex-snapshot
Endocytosis regulation by autophagy proteins in MHC restricted antigen presentation
inferredcites →https://doi.org/10.1016/j.coi.2019.01.001openalex-snapshot
MHC I chaperone complexes shaping immunity
inferredcites →https://doi.org/10.1016/j.coi.2020.04.004openalex-snapshot
Structural and dynamic studies of TAPBPR and Tapasin reveal the mechanism of peptide loading of MHC-I molecules
inferredcites →https://doi.org/10.1016/j.patbio.2009.11.001openalex-snapshot
Pathogenesis of hepatitis B virus infection
inferredcites →https://doi.org/10.1016/j.vaccine.2010.03.070openalex-snapshot
The delivery of HBcAg via Tat-PTD enhances specific immune response and inhibits Hepatitis B virus replication in transgenic mice
inferredcites →https://doi.org/10.1038/ni.3273openalex-snapshot
Autophagy and autophagy-related proteins in the immune system
inferredcites →https://doi.org/10.1038/s41467-018-03037-xopenalex-snapshot
Non-equivalent antigen presenting capabilities of dendritic cells and macrophages in generating brain-infiltrating CD8 + T cell responses
inferredcites →https://doi.org/10.1038/s41598-017-16609-6openalex-snapshot
Exosomes from antigen-pulsed dendritic cells induce stronger antigen-specific immune responses than microvesicles in vivo
inferredcites →https://doi.org/10.1053/j.gastro.2018.06.093openalex-snapshot
Cell and Animal Models for Studying Hepatitis B Virus Infection and Drug Development
inferredcites →https://doi.org/10.1073/pnas.1807656116openalex-snapshot
Successive crystal structure snapshots suggest the basis for MHC class I peptide loading and editing by tapasin
inferredcites →https://doi.org/10.1080/15548627.2015.1110666openalex-snapshot
Autophagy regulates T lymphocyte proliferation through selective degradation of the cell-cycle inhibitor CDKN1B/p27Kip1
inferredcites →https://doi.org/10.1080/2162402x.2016.1274476openalex-snapshot
Loss of tapasin in human lung and colon cancer cells and escape from tumor-associated antigen-specific CTL recognition
inferredcites →https://doi.org/10.1111/imm.12165openalex-snapshot
Autophagy in the immune system
inferredcites →https://doi.org/10.1111/imr.12422openalex-snapshot
Autophagy proteins in antigen processing for presentation on MHC molecules
inferredcites →https://doi.org/10.1111/j.1440-1746.2010.06545.xopenalex-snapshot
Treatment of chronic hepatitis B: Evolution over two decades
inferredcites →https://doi.org/10.1146/annurev-immunol-041015-055700openalex-snapshot
Antigen Presentation by Extracellular Vesicles from Professional Antigen-Presenting Cells
inferredcites →https://doi.org/10.1159/000491972openalex-snapshot
An Engineered DC-Targeting Lentivector Induces Robust T Cell Responses and Inhibits HBV Replication in HBV Transgenic Mice via Upregulating T Cell Autophagy
inferredcites →https://doi.org/10.1186/s12943-019-1001-7openalex-snapshot
Exosomes in gastric cancer: roles, mechanisms, and applications
inferredcites →https://doi.org/10.1186/s12974-019-1587-0openalex-snapshot
Exosomes derived from statin-modified bone marrow dendritic cells increase thymus-derived natural regulatory T cells in experimental autoimmune myasthenia gravis
inferredcites →https://doi.org/10.1186/s13045-017-0534-8openalex-snapshot
The crosstalk between autophagic and endo-/exosomal pathways in antigen processing for MHC presentation in anticancer T cell immune responses
inferredcites →https://doi.org/10.23736/s1121-421x.20.02791-9openalex-snapshot
Hepatocellular carcinoma risk in patients with HBV-related liver disease receiving anti-viral therapy
inferredcites →https://doi.org/10.23736/s2724-5985.20.02791-9openalex-snapshot
Hepatocellular carcinoma risk in patients with HBV-related liver disease receiving antiviral therapy
inferredcites →https://doi.org/10.3390/ijms20112754openalex-snapshot
HBV Immune-Therapy: From Molecular Mechanisms to Clinical Applications
inferredcites →https://doi.org/10.3892/mmr.2016.5610openalex-snapshot
Correlation between low tapasin expression and impaired CD8+ T-cell function in patients with chronic hepatitis B
inferredcites →https://doi.org/10.4049/jimmunol.179.4.2242openalex-snapshot
Effective Treatment of Inflammatory Disease Models with Exosomes Derived from Dendritic Cells Genetically Modified to Express IL-4
inferredcites →https://doi.org/10.5812/hepatmon.16161openalex-snapshot
The Fusion Protein of CTP-HBcAg18-27-Tapasin Mediates the Apoptosis of CD8+T Cells and CD8+ T Cell Response in HLA-A2 Transgenic Mice

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.4763508openalex-extracted
Transcriptomics Reveals the Regulatory Effect of Cichoric Acid on Immunosuppressive Diseases Via Mediating Macrophage-Derived Exosomes
inferred← citeshttps://doi.org/10.1002/jmv.29659openalex-snapshot
Autophagy‐related protein 5 (ATG5) interacts with bone marrow stromal cell antigen 2 (BST2) to stimulate HBV replication through antagonizing the antiviral activity of BST2
inferred← citeshttps://doi.org/10.1016/j.prp.2025.156025openalex-snapshot
A review of the progress and challenges of developing dendritic-based vaccines against hepatitis B virus (HBV)
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