Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal Vaccine

Background. Group A streptococcus (GAS) infections and poststreptococcal sequelae remain a health problem worldwide, which necessitates searching for an effective vaccine, while no licensed GAS vaccine is available. We have developed a divalent peptide vaccine composed of 84 amino acids to cover the...

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Main Authors: Yongxiang Wu, Suhua Li, Yanting Luo, Yunyue Zhao, Jiarui Wang, Ruimin Dong, Xujing Xie, Jieming Zhu, Jinlai Liu
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Canadian Journal of Infectious Diseases and Medical Microbiology
Online Access:http://dx.doi.org/10.1155/2018/4702152
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author Yongxiang Wu
Suhua Li
Yanting Luo
Yunyue Zhao
Jiarui Wang
Ruimin Dong
Xujing Xie
Jieming Zhu
Jinlai Liu
author_facet Yongxiang Wu
Suhua Li
Yanting Luo
Yunyue Zhao
Jiarui Wang
Ruimin Dong
Xujing Xie
Jieming Zhu
Jinlai Liu
author_sort Yongxiang Wu
collection DOAJ
description Background. Group A streptococcus (GAS) infections and poststreptococcal sequelae remain a health problem worldwide, which necessitates searching for an effective vaccine, while no licensed GAS vaccine is available. We have developed a divalent peptide vaccine composed of 84 amino acids to cover the main GAS serotypes (M1 and M12 streptococci) in China, and herein, we aimed to evaluate immunogenicity and safety of this vaccine. Methods. Mice were immunized with the vaccine. ELISA, indirect bactericidal test, and immunofluorescent assay were used to study immunogenicity. GAS challenge assay was used to test the protective effect. Safety was tested by histopathological analysis. Results. Immunized group mice (n=16) developed higher titer antibody after immunization than nonimmunized group mice (n=16) did. This antibody can deposit on the surface of GAS and promote killing of GAS, resulting in 93.1% decrease of M1 GAS and 89.5% of M12 GAS. When challenged with M1 and M12 streptococci, immunized group mice had a higher survival rate (87.5% and 75%) than nonimmunized group mice (37.5% and 25%). No autoimmune reactions were detected on organs of mice. Conclusion. The results suggest that this vaccine shows fair immunogenicity and safety, which will lead our research on GAS vaccine into clinical trial.
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spelling doaj-art-9b17a64d152c42e182e5a436a7e409a32025-08-20T02:20:25ZengWileyCanadian Journal of Infectious Diseases and Medical Microbiology1712-95321918-14932018-01-01201810.1155/2018/47021524702152Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal VaccineYongxiang Wu0Suhua Li1Yanting Luo2Yunyue Zhao3Jiarui Wang4Ruimin Dong5Xujing Xie6Jieming Zhu7Jinlai Liu8Department of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaDepartment of Cardiology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, ChinaBackground. Group A streptococcus (GAS) infections and poststreptococcal sequelae remain a health problem worldwide, which necessitates searching for an effective vaccine, while no licensed GAS vaccine is available. We have developed a divalent peptide vaccine composed of 84 amino acids to cover the main GAS serotypes (M1 and M12 streptococci) in China, and herein, we aimed to evaluate immunogenicity and safety of this vaccine. Methods. Mice were immunized with the vaccine. ELISA, indirect bactericidal test, and immunofluorescent assay were used to study immunogenicity. GAS challenge assay was used to test the protective effect. Safety was tested by histopathological analysis. Results. Immunized group mice (n=16) developed higher titer antibody after immunization than nonimmunized group mice (n=16) did. This antibody can deposit on the surface of GAS and promote killing of GAS, resulting in 93.1% decrease of M1 GAS and 89.5% of M12 GAS. When challenged with M1 and M12 streptococci, immunized group mice had a higher survival rate (87.5% and 75%) than nonimmunized group mice (37.5% and 25%). No autoimmune reactions were detected on organs of mice. Conclusion. The results suggest that this vaccine shows fair immunogenicity and safety, which will lead our research on GAS vaccine into clinical trial.http://dx.doi.org/10.1155/2018/4702152
spellingShingle Yongxiang Wu
Suhua Li
Yanting Luo
Yunyue Zhao
Jiarui Wang
Ruimin Dong
Xujing Xie
Jieming Zhu
Jinlai Liu
Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal Vaccine
Canadian Journal of Infectious Diseases and Medical Microbiology
title Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal Vaccine
title_full Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal Vaccine
title_fullStr Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal Vaccine
title_full_unstemmed Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal Vaccine
title_short Immunogenicity and Safety of a Chemically Synthesized Divalent Group A Streptococcal Vaccine
title_sort immunogenicity and safety of a chemically synthesized divalent group a streptococcal vaccine
url http://dx.doi.org/10.1155/2018/4702152
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