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A novel staphylococcal enterotoxin B subunit vaccine candidate elicits protective immune response in a mouse model.
Choi, Jun Young; Shin, Sungho; Kim, Na Young; Son, Woo Sung; Kang, Tae Jin; Song, Dong Hyun; Yu, Chi Ho; Hur, Gyeung Haeng; Jeong, Seong Tae; Shin, Young Kee.
Afiliación
  • Choi JY; Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, Republic of Korea.
  • Shin S; Bio-MAX/N-Bio, Seoul National University, Seoul, Republic of Korea.
  • Kim NY; ABION Inc., R&D Center, Seoul, Republic of Korea.
  • Son WS; Department of Pharmacy, College of Pharmacy, CHA University, Pocheon-si, Republic of Korea.
  • Kang TJ; College of Pharmacy, Sahmyook University, Seoul, Republic of Korea.
  • Song DH; Agency for Defense Development, Republic of Korea.
  • Yu CH; Agency for Defense Development, Republic of Korea.
  • Hur GH; Agency for Defense Development, Republic of Korea.
  • Jeong ST; Agency for Defense Development, Republic of Korea.
  • Shin YK; Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, Republic of Korea; Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Republic of Korea; Bio-MAX/N-Bio, Seoul
Toxicon ; 131: 68-77, 2017 Jun 01.
Article en En | MEDLINE | ID: mdl-28359755
Staphylococcal enterotoxin B (SEB), produced by the gram-positive bacterium Staphylococcus aureus, is responsible for food poisoning and toxic shock syndrome, and is considered a potential bioterrorism agent. Unfortunately, still now no approved vaccines are available against SEB. In this study, we constructed a series of nontoxic SEB mutants (mSEBs) and examined whether these mSEBs provide protective immunity against SEB challenge. These mSEB vaccine candidates did not demonstrate superantigen activity in mouse splenocyte cultures. Immunization with the vaccine candidates triggered the production of IgG-antibodies with neutralizing activity. In addition, increased production of IgG1 and IgG3 was observed after immunization, which signifies both Th1- and Th2-induced immune responses. Among the vaccine candidates tested, S9, a double mutant (N23A and Y90A) and S19, a quadruple mutant (N23A, Y90A, R110A, and F177A), demonstrated complete protection against a lethal SEB challenge. Altogether, our results strongly suggest that these mSEBs could be an effective recombinant SEB vaccine candidates for further/future preclinical and clinical studies.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Choque Séptico / Intoxicación Alimentaria Estafilocócica / Vacunas Estafilocócicas / Enterotoxinas Límite: Animals Idioma: En Revista: Toxicon Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Choque Séptico / Intoxicación Alimentaria Estafilocócica / Vacunas Estafilocócicas / Enterotoxinas Límite: Animals Idioma: En Revista: Toxicon Año: 2017 Tipo del documento: Article