CD154 ELEVATING CELLULAR IMMUNITY BY UP-REGULATING THE PERCENTAGES OF ANTIGEN-SPECIFIC POSITIVE INTERFERON-GAMMA EXPRESSING CELLS
DOI:
https://doi.org/10.20319/icrlsh.2025.12Abstract
CD154 plays a central role in the development and regulation of adaptive immune responses in mammals and thus may act as a potential molecular adjuvant due to its enhancement of cytokine expression in immune cells. In this study, CD154-coding sequence was linked with the E2 antigen sequence of the Classical swine fever virus (CSFV) to produce an E2-CD154 vaccine and the specific pathogen free piglets at the age of 4-week old was used as an animal model. The CpG adjuvant, a Toll-like receptor 9 agonist, was used as a positive control. The animals were randomized into three groups and primarily vaccinated with E2-CD154, E2-CpG or the commercial Bayovac® E2 vaccines, respectively. All animals were boosted 2 weeks after primary vaccination. Results showed that the percentages of CD3+CD4+, CD4+IL2+ and CD4+IFNγ+ T cells in the peripheral blood mononuclear cells on 7-d (7 days) after primary vaccination were significantly enhanced in the E2-CD154 group as compared with the other two groups. Noteworthy, CD8+IL-2+ populations were increased on 21-d and CD4+IL2+ showed the highest expression on 28-d after booster in those of the E2-CD154 group. In addition, significantly increased E2-specific IFNγ+ cells were found on 10-d and 14-d after the primary vaccination and 21-d and 28-d after booster in those of the E2-CD154 group. These results indicate that CD154 elevated T cells activities for producing high levels of IL-2 and IFN-γ. Thus, CD154 may act as a potential immunomodulatory adjuvant by increasing antigen-specific positive IFNγ-expressing cells.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Yu-Chieh Chen, Li-Yun Wang, Chi-Chih Chen, Dao Huy Hung, Ya-Mei Chen, Wen-Bin Chung, Hso-Chi Chaung, Guan-Ming Ke

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Copyright of Published Articles
Author(s) retain the article copyright and publishing rights without any restrictions.
All published work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.