AI Article Synopsis

  • The study investigates the effect of combining spermidine (SPD) with vaccine adjuvants on enhancing the immune response to HBV vaccination in mice.
  • Administering HBsAg with SPD and either cGAMP or K3-SPG significantly boosted interferon-γ production and increased serum HBsAb levels.
  • The findings suggest that this combination could potentially strengthen the immune response and aid in the complete elimination of HBV from infected individuals.

Article Abstract

Unlabelled: Background: Various vaccine adjuvants have been developed to eliminate HBV from patients with chronic HBV infection. In addition, spermidine (SPD), a type of polyamine, has been reported to enhance the activity of immune cells. In the present study, we investigated whether the combination of SPD and vaccine adjuvant enhances the HBV antigen-specific immune response to HBV vaccination. Methods: Wild-type and HBV-transgenic (HBV-Tg) mice were vaccinated 2 or 3 times. SPD was orally administered in drinking water. Cyclic guanosine monophosphate-AMP (cGAMP) and nanoparticulate CpG-ODN (K3-SPG) were used as the HBV vaccine adjuvants. The HBV antigen-specific immune response was evaluated by measuring the HBsAb titer in blood collected over time and the number of interferon-γ producing cells by enzyme-linked immunospot assay. Results: The administration of HBsAg + cGAMP + SPD or HBsAg + K3-SPG + SPD significantly enhanced HBsAg-specific interferon-γ production by CD8 T cells from wild-type and HBV-Tg mice. The administration of HBsAg, cGAMP, and SPD increased serum HBsAb levels in wild-type and HBV-Tg mice. In HBV-Tg mice, the administration of SPD + cGAMP or SPD + K3-SPG with HBV vaccination significantly reduced HBsAg levels in the liver and serum.

Conclusions: These results indicate that the combination of HBV vaccine adjuvant and SPD induces a stronger humoral and cellular immune response through T-cell activation. These treatments may support the development of a strategy to completely eliminate HBV.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043579PMC
http://dx.doi.org/10.1097/HC9.0000000000000104DOI Listing

Publication Analysis

Top Keywords

hbv-tg mice
16
hbv vaccination
12
immune response
12
cgamp spd
12
hbv
10
spd
9
vaccine adjuvants
8
eliminate hbv
8
vaccine adjuvant
8
hbv antigen-specific
8

Similar Publications

Ethnopharmacological Relevance: Chronic hepatitis B virus (HBV) infection is still a widespread global health issue. HuaganJiedu Decoction (HGJDD) is a common prescription for treating HBV in China, which has the effect of enhancing antiviral efficacy and improving clinical efficacy. However, its precise mechanism of action remains unclear, warranting further investigation to elucidate its therapeutic potential and integration into standard medical practices.

View Article and Find Full Text PDF
Article Synopsis
  • - Liver fibrosis linked to hepatitis B can lead to serious liver cancer, and menstrual blood-derived stem cells (MenSCs) have shown promise in alleviating this condition by promoting healing in liver tissues.
  • - A study using a mouse model of liver fibrosis showed that MenSCs migrated to injured areas, improving liver function and reducing fibrosis through changes in cell interactions and matrix proteins.
  • - Advanced techniques like single-cell RNA sequencing and CellChat analysis revealed the complex interactions between different cell types in the liver, suggesting specific molecules that can be targeted for future therapies using MenSCs.
View Article and Find Full Text PDF

Background: Podocytes, as intrinsic renal cells, can also express MHC-II and costimulatory molecules under inflammatory conditions, suggesting that they may act as antigen-presenting cells (APCs) to activate immune cell responses and then lead to immune-mediated renal injury. They are already recognized as main targets in the pathogenic mechanism of hepatitis B virus (HBV)-associated glomerulonephritis (HBV-GN). Previous studies also have indicated that inflammatory cells infiltration and immune-mediated tissue injury are evident in the kidney samples of patients with HBV-GN.

View Article and Find Full Text PDF

Stat3 activation-triggered transcriptional networks govern the early stage of HBV-induced hepatic inflammation.

mBio

April 2024

Department of Infectious Diseases, Key Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Unlabelled: The chronic carrier state of the hepatitis B virus (HBV) often leads to the development of liver inflammation as carriers age. However, the exact mechanisms that trigger this hepatic inflammation remain poorly defined. We analyzed the sequential processes during the onset of liver inflammation based on time-course transcriptome and transcriptional regulatory networks in an HBV transgenic (HBV-Tg) mice model and chronic HBV-infected (CHB) patients (data from GSE83148).

View Article and Find Full Text PDF

RNA-binding motif protein 24 inhibits HBV replication in vivo.

J Med Virol

July 2023

State Key Laboratory of Virology, Center for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.

Despite the extensive use of effective vaccines and antiviral drugs, chronic hepatitis B virus (HBV) infection continues to pose a serious threat to global public health. Therapies with novel mechanisms of action against HBV are being explored for achieving a functional cure. In this study, five murine models of HBV replication were used to investigate the inhibitory effect of RNA binding motif protein 24 (RBM24) on HBV replication.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!