Aug 2026· Vaccine· Vol 91, pp.
129073
· 0 citations· 60 references
Medicine
TL;DR
Combining AddaS03 and Poly I:C adjuvants is a potent strategy to modulate and enhance immune responses elicited by an RBD-based vaccine.
Abstract
Background
The COVID-19 pandemic caused over seven million deaths, and disease control relied largely on mass immunization campaigns. Although diverse vaccine platforms were used, most formulations targeted the Spike protein because of its central role in virus entry. Persistent viral evolution and global vaccine inequity highlight the need for alternative strategies, particularly for low- and middle-income countries. In this scenario, recombinant protein-based vaccines are attractive due to low cost, established manufacturing pipelines and well-characterized safety profiles. The receptor binding domain (RBD) of Spike is an appealing antigen due to its relatively simple structure, proven immunogenicity - especially in multimerized formats - and because it harbors most neutralizing antibody epitopes. Protein-based vaccines, however, rely on the use of adjuvants to optimize antigen-specific immunity.
Methods
We used an RBD dimer derived from the ancestral Wuhan strain as a well-characterized protein to evaluate the humoral and cellular immunogenicity of combined AddaS03 and Poly I:C adjuvants in BALB/c mice.
Results
The adjuvant combination preserved the strong humoral responses typically induced by AddaS03 while conferring the Th1-skewing properties of Poly I:C, producing a synergistic effect that exceed those of each adjuvant alone. Specifically, the combination improved antibody affinity, increased the generation of antibody- secreting cells in spleen and bone marrow, and enhanced the induction of polyfunctional, cytokine-producing CD4+ T cells. Additionally, we mapped and characterized three class II T cell epitopes within RBD: peptide 6 (351-YAWNRKRISNCVADYSV-367), peptide 19 (442-SKVGGNYNYLYRLFRK-458) and peptide 20 (449-YNYLYRLFRKSNLKPFE-465).
Conclusions
Combining AddaS03 and Poly I:C adjuvants is a potent strategy to modulate and enhance immune responses elicited by an RBD-based vaccine.
The preclinical development of a novel HCV vaccine candidate engineered by formulating a novel native-like secreted E1E2 immunogen and a well-established combinatorial adjuvant of QS-21 + 3D-(6-acyl) PHAD into unique microneedle patches (MNPs).
Yi-Nuo Zhang, A. Dhayani, Stephen C. Balmert et al.· Journal of Immunology· 0 citations
Results demonstrate that AZD6563, at reduced doses, matches the cellular immunogenicity of BNT162b2 while enhancing B cell cross-reactivity and TCR diversity in older adults, supporting its potential as a next-generation COVID-19 vaccine candidate.
Michael D. Powell, Nicholas G. Battaglia, Lee-Jah Chang et al.· Journal of Immunology· 0 citations
It is shown that a Wuhan-lineage-based multi-antigen VLP vaccine can provide cross-protection against an antigenically divergent SARS-CoV-2 variant that is not fully explained by detectable serum neutralizing activity alone, suggesting the importance of integrated immune responses involving humoral, cellular, and local...
Seung-Ji Kim, Howon Kim, Seung-Eun Son et al.· Vaccine· 0 citations
Pre-clinical findings demonstrate that the S1-N-T4f fusion antigen is a promising vaccine candidate for further evaluation of its protective potential against PEDV infection.
Mario Fragoso-Saavedra, Brittany Thivierge, Qiang Liu· Microbial Pathogenesis· 0 citations
It is established that the vaccine formulation can effectively boost and redirect pre-existing immunity, offering a promising approach to overcome the limitations of natural exposure and protect at-risk individuals from diverse Pa infections.
D. R. Howlader, Sayan Das, Satabdi Biswas et al.· Infection and Immunity· 0 citations
Intramuscular mRNA vaccines show superior safety, while spike contains epitopes capable of driving Th2- and Th17-mediated pathology, highlighting the need to refine spike antigens and booster strategies for durable, safe protection.
Tian-Yi Zhang, Nicholas Magazine, Lamis El-Baz et al.· Journal of Immunology· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.