CD154 ELEVATING CELLULAR IMMUNITY BY UP-REGULATING THE PERCENTAGES OF ANTIGEN-SPECIFIC POSITIVE INTERFERON-GAMMA EXPRESSING CELLS

Authors

  • Yu-Chieh Chen Research Center for Animal Biologics, NPUST, Pingtung, Taiwan
  • Li-Yun Wang Research Center for Animal Biologics, NPUST, Pingtung, Taiwan
  • Chi-Chih Chen Research Center for Animal Biologics, NPUST, Pingtung, Taiwan
  • Dao Huy Hung Department of veterinary medicine, NPUST, Pingtung, Taiwan
  • Ya-Mei Chen Department of veterinary medicine, NPUST, Pingtung, Taiwan
  • Wen-Bin Chung Department of veterinary medicine, NPUST, Pingtung, Taiwan
  • Hso-Chi Chaung Department of veterinary medicine, NPUST, Pingtung, Taiwan
  • Guan-Ming Ke International Degree Program in Animal Vaccine Technology, NPUST, Pingtung, Taiwan

DOI:

https://doi.org/10.20319/icrlsh.2025.12

Abstract

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.

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Published

2025-06-12

How to Cite

Yu-Chieh Chen, Li-Yun Wang, Chi-Chih Chen, Dao Huy Hung, Ya-Mei Chen, Wen-Bin Chung, Hso-Chi Chaung, & Guan-Ming Ke. (2025). CD154 ELEVATING CELLULAR IMMUNITY BY UP-REGULATING THE PERCENTAGES OF ANTIGEN-SPECIFIC POSITIVE INTERFERON-GAMMA EXPRESSING CELLS. LIFE: International Journal of Health and Life-Sciences, 1–2. https://doi.org/10.20319/icrlsh.2025.12