• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

Emerg Microbes Infect . Receptor binding domain-independent pancoronavirus vaccine design by fusion of conserved T/B Epitopes

tetano

Editor, Senior Moderator
Emerg Microbes Infect


. 2026 Feb 11:2631206.
doi: 10.1080/22221751.2026.2631206. Online ahead of print.
Receptor binding domain-independent pancoronavirus vaccine design by fusion of conserved T/B Epitopes

Yunru Yang[SUP] 1 [/SUP], Yetian Chen[SUP] 2 3 [/SUP], Mengyu Hong[SUP] 2 4 [/SUP], Ronghua Zou[SUP] 4 [/SUP], Jingxue Yao[SUP] 2 4 [/SUP], Entao Li[SUP] 5 [/SUP], Jiayi Wang[SUP] 6 [/SUP], Xiaodong Ye[SUP] 6 [/SUP], Yixiang Xing[SUP] 7 [/SUP], Yangming Tang[SUP] 8 [/SUP], Xiaojie Lu[SUP] 8 [/SUP], Chengchao Ding[SUP] 1 [/SUP], Hongliang He[SUP] 1 [/SUP], Dali Tong[SUP] 9 [/SUP], Yuhua Shang[SUP] 3 [/SUP], Jian Wang[SUP] 10 [/SUP], Guangyu Zhao[SUP] 11 [/SUP], Xiaoxue Huang[SUP] 2 4 [/SUP], Fuli Feng[SUP] 12 [/SUP], Qingyu Cheng[SUP] 4 [/SUP], Bofeng Li[SUP] 1 5 [/SUP], Baoying Huang[SUP] 13 [/SUP], Wenjie Tan[SUP] 13 [/SUP], Sandra Chiu[SUP] 5 10 14 [/SUP], Tengchuan Jin[SUP] 1 2 3 4 5 14 15 16 [/SUP]


Affiliations
Free article Abstract

The persistent emergence of SARS-CoV-2 variants continues to compromise current vaccine efficacy, driving the development of broad-spectrum coronavirus vaccines to address variant evasion and future outbreaks. To develop a pan-coronavirus vaccine, we identified some conserved T/B epitopes across spike proteins of human-infecting coronaviruses, focusing on two conserved long peptides, VV and VS, which demonstrated broad immunogenicity in PBMCs from COVID-19 convalescent patients. By structurally fusing the VV and VS long peptides with heptad repeat 1/2 (HR1/2) domains from the S2 subunit, we engineered a trimeric immunogen HR1-VV-HR2-VS. This design induced superior cellular and humoral immune responses compared to individual peptide components in immunized mice. The vaccine also significantly reduced viral loads and attenuated lung pathology in mice challenged with HCoV-229E, SARS-CoV-2 prototype strain, and the KP.2 variant, demonstrating cross-protective immunity. Therefore, these results indicated that HR1-VV-HR2-VS vaccine elicits cross-protective immunity, highlighting its potential as a universal coronavirus vaccine. In addition, we developed an innovative peptide vaccine platform based on the HR1-HR2 trimeric structural protein, which serves as a potent polypeptide fusion scaffold to significantly enhance peptide immunogenicity.

Keywords: Cross-protective; Epitopes; Fusion protein; Pancoronavirus; Vaccine.

 
Back
Top Bottom