A novel staphylococcal enterotoxin B subunit vaccine candidate elicits protective immune response in a mouse model

被引:13
|
作者
Choi, Jun Young [1 ]
Shin, Sungho [3 ]
Kim, Na Young [4 ]
Son, Woo Sung [5 ]
Kang, Tae Jin [6 ]
Song, Dong Hyun [7 ]
Yu, Chi Ho [7 ]
Hur, Gyeung Haeng [7 ]
Jeong, Seong Tae [7 ]
Shin, Young Kee [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Res Inst Pharmaceut Sci, Coll Pharm, Seoul 08826, South Korea
[2] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, Mol Med & Biopharmaceut Sci, Seoul, South Korea
[3] Seoul Natl Univ, BioMAX N Bio, Seoul, South Korea
[4] ABION Inc, R&D Ctr, Seoul, South Korea
[5] CHA Univ, Dept Pharm, Coll Pharm, Pocheon Si, South Korea
[6] Sahmyook Univ, Coll Pharm, Seoul, South Korea
[7] Agcy Def Dev, Seoul, Daejeon, South Korea
关键词
Mutation; Recombinant vaccine; Staphylococcal enterotoxin B; Vaccine candidates; STRUCTURAL BASIS; SUPERANTIGEN; IMMUNIZATION; MUTANTS; MUCOSAL; COMPLEX; TOXINS;
D O I
10.1016/j.toxicon.2017.03.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 Thl- 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. (C) 2017 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:68 / 77
页数:10
相关论文
共 50 条
  • [31] SUPPRESSION OF INVIVO HUMORAL AND CELLULAR IMMUNE-RESPONSE BY STAPHYLOCOCCAL ENTEROTOXIN-B (SEB)
    PINTO, M
    TORTEN, M
    BIRNBAUM, SC
    TRANSPLANTATION, 1978, 25 (06) : 320 - 323
  • [32] Analysis of the in vivo dendritic cell response to the bacterial superantigen staphylococcal enterotoxin B in the mouse spleen
    Yoon, S
    Bae, KL
    Shin, JY
    Yoo, HJ
    Lee, HW
    Baek, SY
    Kim, BS
    Kim, JB
    Lee, HD
    HISTOLOGY AND HISTOPATHOLOGY, 2001, 16 (04) : 1149 - 1159
  • [33] An MPXV m RNA-LNP vaccine candidate elicits protective immune responses against monkeypox virus
    Yuxin Tian
    Mengjun Li
    Yang Yang
    Chunhui Li
    Yun Peng
    Haiyin Yang
    Mengyuan Zhao
    Pengfei Wu
    Shaobo Ruan
    Yuanyu Huang
    Chenguang Shen
    Minghui Yang
    ChineseChemicalLetters, 2024, 35 (08) : 493 - 497
  • [34] Exploring the Influence of Hepatitis B Immunoglobulin on the Immune Response to the Hepatitis B Vaccine in a Mouse Model
    Wei, Tao
    Lv, Wei-Hong
    Gao, Mei-Hua
    Tan, Shan-Juan
    Li, Ling
    Zhang, Lei
    IRANIAN JOURNAL OF IMMUNOLOGY, 2023, 20 (01) : 67 - 75
  • [35] Characterization and protective efficacy in an animal model of a novel truncated rotavirus VP8 subunit parenteral vaccine candidate
    Xue, Miaoge
    Yu, Linqi
    Che, Yaojian
    Lin, Haijun
    Zeng, Yuanjun
    Fang, Mujin
    Li, Tingdong
    Ge, Shengxiang
    Xia, Ningshao
    VACCINE, 2015, 33 (22) : 2606 - 2613
  • [36] Electroporation of a multivalent DNA vaccine cocktail elicits a protective immune response against anthrax and plague
    Albrecht, Mark T.
    Livingston, Brian D.
    Pesce, John T.
    Bell, Matt G.
    Hannaman, Drew
    Keane-Myers, Andrea M.
    VACCINE, 2012, 30 (32) : 4872 - 4883
  • [37] Kinetics of cellular and cytokine responses in a chimeric mouse model for the study of staphylococcal enterotoxin B pathogenesis
    Yuan, L
    Lowell, GH
    Hoover, DL
    Colleton, CA
    Hammack, CA
    Young, LD
    Fischer, R
    Patchen, ML
    Cross, AS
    IMMUNOLOGY LETTERS, 2000, 71 (01) : 19 - 26
  • [38] Immune response with biodegradable nanospheres and alum: studies in rabbits using staphylococcal enterotoxin B-toxoid
    Desai, MP
    Hilfinger, JM
    Amidon, GL
    Levy, RJ
    Labhasetwar, V
    JOURNAL OF MICROENCAPSULATION, 2000, 17 (02) : 215 - 225
  • [39] A Recombinant Chimera Protein as a Novel Brucella Subunit Vaccine: Protective Efficacy and Induced Immune Response in BALB/c Mice
    Abdollahi, Abbas
    Mansouri, Shahla
    Amani, Jafar
    Fasihi-Ramandi, Mandi
    Ranjbar, Reza
    Ghasemi, Amir
    Moradi, Mohammad
    JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 2018, 11 (01) : 1 - 9
  • [40] Staphylococcal enterotoxin B mutants (N23K and F44S): Biological effects and vaccine potential in a mouse model
    Woody, MA
    Krakauer, T
    Stiles, BG
    VACCINE, 1997, 15 (02) : 133 - 139