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    Student seminar - Immunogenicity and protective efficacy of inactivated coxsackievirus B4 viral particles

    Date:Apr 26, 2024   |  【 A  A  A 】  |  【Print】 【Close】

    Reporter:  WANG Tingfeng 

    Supervisor:   LIANG Xiaozhen

    Title: Immunogenicity and protective efficacy of inactivated coxsackievirus B4 viral particles

    Time: April 26, 2024 13:00-14:00

    Introduction:

    Coxsackievirus B4 (CVB4) is associated with a range of acute and chronic diseases such as hand, foot, and mouth disease, myocarditis, meningitis, pancreatitis, and type 1 diabetes, affecting millions of young children annually around the world. However, no vaccine is currently available for preventing CVB4 infection. Here, we report the development of inactivated viral particle vaccines for CVB4. Two types of inactivated CVB4 particles were prepared from CVB4-infected cell cultures as vaccine antigens, including F-particle and E-particle. Both the inactivated CVB4 F-particle and E-particle were able to potently elicit neutralizing antibodies in mice. Importantly, we demonstrated that passive transfer of either anti-F-particle or anti-E-particle sera could completely protect the recipient mice from lethal CVB4 challenge. Our study not only defines the immunogenicity and protective efficacy of inactivated CVB4 F-particle and E-particle but also reveals the central role of neutralizing antibodies in anti-CVB4 protective immunity, thus providing important information that may accelerate the development of inactivated CVB4 vaccines.

     

     

     


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