Ruichen Gao

Ms. Ruichen Gao


Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 July 2025 in Biology
Verified
Journal Article
Open access
PDF file
RGRuichen Gao
Ruichen Gao
WSWei Sun
Wei Sun
DZDanning Zhang
Danning Zhang
LZLinhan Zhang
Linhan Zhang
HDHe Dafang
He Dafang
GWGang Wang
Gang Wang
The feline calicivirus, herpesvirus, and panleukopenia viruses are major infections that cause serious diseases in cats; however, current trivalent vaccines have limitations in immune efficacy and their duration of protection. This study assesses the immune-enhancing effects of novel adjuvants (feline IL-15, IL-23, and metabolic modulators) on vaccine responses. Forty mice were randomly assigned to four groups: Group A (composite adjuvants), Group B (metabolic regulatory molecules and Mn adjuvant), Group C1 (Mn adjuvant), and Group C2 (a blank commercial vaccine). The results showed that Group A had significantly higher neutralizing antibody titers against calicivirus post-booster immunization, while both Groups A and B exhibited enhanced antibody responses against the herpesvirus and panleukopenia viruses. Notably, Group A displayed increased proportions of memory T cells, follicular B cells, and activated B cells. These findings suggest that the combination of feline IL-15, IL-23, and metabolic modulators are safe and effective immunoadjuvants for trivalent feline vaccines to promote immune cell differentiation and antibody production, thus representing a promising strategy to optimize vaccine efficacy.

16 April 2025 in Preprints.org
Verified
Preprint
Open access
PDF file
RGRuichen Gao
Ruichen Gao
WSWei Sun
Wei Sun
DZDanning Zhang
Danning Zhang
LZLinhan Zhang
Linhan Zhang
HDHe Dafang
He Dafang
XLXuebin Lv
Xuebin Lv
Feline calicivirus, herpesvirus, and panleukopenia virus are major infectious viruses to cause serious diseases in cats, yet their current trivalent vaccines have limitations in immune efficacy and duration of protection. This study assessed the immune-enhancing effects of novel adjuvants (feline IL-15, IL-23, and metabolic modulators) on vaccine responses. Forty mice were randomly assigned to four groups: Group A (composite adjuvants), Group B (metabolic regulatory molecules and Mn adjuvant), Group C1 (Mn adjuvant), and Group C2 (blank commercial vaccine). Results showed that Group A had significantly higher neutralizing antibody titers against calicivirus post-booster immunization, while both Group A and B exhibited enhanced antibody responses against herpesvirus and parvovirus. Notably, Group A displayed increased proportions of memory T cells, follicular B cells, and activated B cells. These findings suggest that the combination of feline IL-15, IL-23, and metabolic modulators are safe and effective immunoadjuvants for the trivalent feline vaccines to promote immune cell differentiation and antibody production, thus representing a promising strategy to optimize vaccine efficacy.