Background: The cytotoxic T lymphocyte antigen 4 (CTLA4) represents an attractive ligand for use in the targeting of antigens to dendritic cells (DCs). Studies have shown that CTLA4 targeted DNA vaccines induced accelerated and increased antibody responses compared to nontargeted vaccines. However, little is known about the molecular events on DCs after transfection with targeted DNA vaccines.
Methods: Here we constructed a green fluorescent protein (GFP)-labeled targeted anti-caries plasmid pMGJGLU/GFP and a GFP-labeled nontargeted anti-caries plasmid pCDGLU/GFP, compared the antibody responses they induced in mice, and investigated the gene expression profiles of DCs transfected with pMGJGLU/GFP and pCDGLU/GFP by gene array analysis.
Results: The data obtained showed that pMGJGLU/GFP induced accelerated and increased serum antibody responses in mice compared to pCDGLU/GFP. Overall, the expression levels of 28 genes were up-regulated in pMGJGLU/GFP transfected DCs compared to pCDGLU/GFP transfected DCs by gene array analysis. Real-time reverse transcriptase-polymerase chain reaction analysis on pMGJGLU/GFP transfected DCs and pCDGLU/GFP transfected DCs confirmed the up-regulation of the mRNA expression levels of seven selected genes. Notably, we identified the specific up-regulation of mRNA expression levels of cytokines Ccl17, Ccl19, and antigen presentation receptor Cd209a of pMGJGLU/GFP transfected DCs, suggesting a more rapid migration of DCs to lymph nodes and a T helper 2 biased immune response.
Conclusions: In the present study, we confirmed our previous reports that CTLA4 targeted DNA vaccines could induce increased antibody responses compared to nontargeted vaccines. Ccl17, Ccl19 and Cd209a may play an important role in the enhanced immune responses.
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http://dx.doi.org/10.1002/jgm.1308 | DOI Listing |
Hum Vaccin Immunother
December 2025
Research and Development, Infectious Disease, Moderna, Inc., Cambridge, MA, USA.
Safety, immunogenicity, and effectiveness of an mRNA-1273 50-μg booster were evaluated in adolescents (12-17 years), with and without pre-booster SARS-CoV-2 infection. Participants who had received the 2-dose mRNA-1273 100-µg primary series in the TeenCOVE trial (NCT04649151) were offered the mRNA-1273 50-μg booster. Primary objectives included safety and inference of effectiveness by establishing noninferiority of neutralizing antibody (nAb) responses after the booster compared with the nAb post-primary series of mRNA-1273 among young adults in COVE (NCT04470427).
View Article and Find Full Text PDFAm J Respir Cell Mol Biol
January 2025
Wayne State University, Division of Pulmonary, Critical Care and Sleep Medicine, Detroit, Michigan, United States;
Numerous chronic human disorders are associated with immune activation by obscure antigen(s). We identified a novel sarcoidosis-epitope (ChainA) by immunoscreening of a novel T7 phage library and confirmed an abundance of ChainA IgG-antibody in sarcoidosis. We tested whether ChainA epitope elicits immune responses through B-cell activation, plasma cell differentiation and antibody production.
View Article and Find Full Text PDFJ Virol
January 2025
Vaccine and Gene Therapy Institute, Oregon Health & Science University, Beaverton, Oregon, USA.
Kaposi's sarcoma-associated herpesvirus (KSHV) is a human gammaherpesvirus associated with Kaposi's sarcoma and B cell malignancies. Like all herpesviruses, KSHV contains conserved envelope glycoproteins (gps) involved in virus binding, entry, assembly, and release from infected cells, which are also targets of the immune response. Due to the lack of a reproducible animal model of KSHV infection, the precise functions of the KSHV gps during infection are not completely known.
View Article and Find Full Text PDFPain
December 2024
Palo Alto Veterans Institute for Research, Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, United States.
Previous preclinical and translational studies suggest that tissue trauma related to bony fracture and intervertebral disk disruption initiates the formation of pronociceptive antibodies that support chronic musculoskeletal pain conditions. This study tested this hypothesis in the monosodium iodoacetate (MIA) mouse model of osteoarthritis (OA) and extended the findings using OA patient samples. Monosodium iodoacetate was injected unilaterally into the knees of male and female wild-type (WT) and muMT mice (lacking B cells) to induce articular cartilage damage.
View Article and Find Full Text PDFFront Immunol
January 2025
Faculty of Medicine, University of Castilla-La Mancha, Albacete, Spain.
Introduction: Despite the efficacy and safety of SARS-CoV-2 vaccines, inflammatory and/or thrombotic episodes have been reported. Since the impact of COVID-19 vaccines on the endothelium remains uncertain, our objective was to assess endothelial activation status before and 90 days after the third dose of the BNT162b2 mRNA COVID-19 vaccine.
Methods: A prospective longitudinal study was conducted at University General Hospital of Albacete, involving 38 healthy health-care workers.
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