Swiss albino mice
Oral or intranasal inoculation with Coxsackievirus B4 (CVB4)
Anti-CVB4 neutralizing activity of serum and saliva, anti-enterovirus IgG and IgA antibodies, and serum-dependent enhancement of CVB4 infectionsurrogate
Mucosal exposure to CVB4 in Swiss albino mice induces both neutralizing and enhancing antibodies, providing a model to test strategies for promoting protective mucosal immunity.
Coxsackieviruses B are single-stranded RNA viruses belonging to the Enterovirus genus and are associated with various clinical outcomes, ranging from acute infections to chronic diseases, such as type 1 diabetes (T1D). It was previously shown that inoculation of Swiss albino mice with CVB4 by the intraperitoneal route induced both anti-CVB4 neutralizing and enhancing activities of serum. This study aimed to investigate the humoral immune response of mice inoculated with CVB4 by the mucosal route. Mice were inoculated orally or intranasally with CVB4, and the anti-CVB4 neutralizing activity of serum and saliva was assessed by a cell culture neutralization assay. Anti-enterovirus (EV) IgG and IgA antibodies were detected in serum and saliva, respectively, by ELISA. The serum-dependent enhancement of CVB4 infection in cultures of murine splenocytes was evaluated by detecting intracellular viral RNA using RT-qPCR. At day 45 post-inoculation, an anti-CVB4 neutralizing activity, the extent of which depends on the amount of inoculated infectious particles, was detected in the serum of mice exposed orally or intranasally. An increase in anti-CVB4 neutralizing activity was observed in the saliva of mice inoculated orally or intranasally during the follow-up. Oral or intranasal inoculation of CVB4 induced a systemic IgG and mucosal IgA response. In addition, serum from these mice harbored an anti-CVB4 enhancing activity in vitro. These data indicate that Swiss albino mice exposed to CVB4 via the mucosal route constitute a potentially useful model for testing strategies to promote the production of protective mucosal and systemic anti-CVB4 antibodies and for verifying whether or not enhanced antibodies are produced.
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Chaldam Jespère Mbani
Magloire Pandoua Nekoua
Laurine Couture
Microorganisms
SHILAP Revista de lepidopterología
Université de Lille
Centre Hospitalier Universitaire de Lille
Marien Ngouabi University
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Mbani et al. (Tue,) studied this question.
www.synapsesocial.com/papers/69a75a9dc6e9836116a20acc — DOI: https://doi.org/10.3390/microorganisms14020289