A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model

被引:7
|
作者
Snow, Doris M. [1 ]
Cobb, Ronald R. [1 ]
Martinez, Juan [1 ]
Finger-Baker, Isaac [1 ]
Collins, Laura [1 ]
Terpening, Sara [1 ]
Syar, Emily S. [2 ]
Niemuth, Nancy [2 ]
Kobs, Dean [2 ]
Barnewall, Roy [2 ]
Farr-Jones, Shauna [3 ]
Marks, James D. [3 ]
Tomic, Milan T. [4 ]
机构
[1] Ology Bioserv, 13200 NW, Alachua, FL 32615 USA
[2] Battelle Biomed Res Ctr, Columbus, OH 43162 USA
[3] Univ Calif San Francisco, Dept Anesthesia & Perioperat Care, 1001 Potrero Ave, San Francisco, CA 94110 USA
[4] Ology Bioserv Inc, Res & Dev, 2061 Challenger Dr, Alameda, CA 94501 USA
关键词
botulinum neurotoxin; aerosol; monoclonal antibody; guinea pig inhalation model; oligoclonal antibody; botulism; DOMAIN-BASED ASSAYS; IMMUNE GLOBULIN; NEUROTOXIN; IDENTIFICATION; VACCINE; NEUTRALIZATION; VOLUNTEERS; PROTECTION; SAFETY;
D O I
10.3390/toxins13010031
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Botulinum neurotoxins (BoNT) are extremely potent and can induce respiratory failure, requiring long-term intensive care to prevent death. Recombinant monoclonal antibodies (mAbs) hold considerable promise as BoNT therapeutics and prophylactics. In contrast, equine antitoxin cannot be used prophylactically and has a short half-life. Two three-mAb combinations are in development that specifically neutralize BoNT serotype A (BoNT/A) and B (BoNT/B). The three-mAb combinations addressing a single serotype provided pre-exposure prophylaxis in the guinea pig inhalation model. A lyophilized co-formulation of six mAbs, designated G03-52-01, that addresses both A and B serotypes is in development. Here, we investigated the efficacy of G03-52-01 to protect guinea pigs against an aerosol exposure challenge of BoNT/A1 or BoNT/B1. Previously, it was found that each antibody demonstrated a dose-dependent exposure and reached maximum circulating concentrations within 48 h after intramuscular (IM) or intravenous (IV) injection. Here we show that G03-52-01, in a single IM injection of G03-52-01 administered 48 h pre-exposure, protected guinea pigs against an aerosol challenge of up to 238 LD(50)s of BoNT/A1 and 191 LD(50)s of BoNT/B1. These data suggest that a single IM administration of G03-52-01 provides pre-exposure prophylaxis against botulism from an aerosol exposure of BoNT/A1 or BoNT/B1.
引用
收藏
页数:16
相关论文
共 10 条
  • [1] Monoclonal Antibody Combinations Prevent Serotype A and Serotype B Inhalational Botulism in a Guinea Pig Model
    Tomic, Milan T.
    Espinoza, Yero
    Martinez, Zachary
    Pham, Khanh
    Cobb, Ronald R.
    Snow, Doris M.
    Earnhart, Christopher G.
    Pals, Traci
    Syar, Emily S.
    Niemuth, Nancy
    Kobs, Dean J.
    Farr-Jones, Shauna
    Marks, James D.
    [J]. TOXINS, 2019, 11 (04)
  • [2] Potency of a human monoclonal antibody to diphtheria toxin relative to equine diphtheria anti-toxin in a guinea pig intoxication model
    Smith, Heidi L.
    Cheslock, Peter
    Leney, Mark
    Barton, Bruce
    Molrine, Deborah C.
    [J]. VIRULENCE, 2016, 7 (06) : 660 - 668
  • [3] A novel neutralizing monoclonal antibody against both ricin toxin A and ricin toxin B, and application of a rapid sandwich enzyme-linked immunosorbent assay
    Guo, Jianwei
    Shen, Beifen
    Feng, Jiannan
    Sun, Yingxun
    Yu, Ming
    Hu, Meiru
    [J]. HYBRIDOMA, 2006, 25 (04): : 225 - 229
  • [4] GUINEA-PIG LINE 10 HEPATO-CARCINOMA MODEL - CHARACTERIZATION OF MONOCLONAL-ANTIBODY AND INVIVO EFFECT OF UNCONJUGATED ANTIBODY AND ANTIBODY CONJUGATED TO DIPHTHERIA TOXIN-A CHAIN
    BERNHARD, MI
    FOON, KA
    OELTMANN, TN
    KEY, ME
    HWANG, KM
    CLARKE, GC
    CHRISTENSEN, WL
    HOYER, LC
    HANNA, MG
    OLDHAM, RK
    [J]. CANCER RESEARCH, 1983, 43 (09) : 4420 - 4428
  • [5] A MONOCLONAL-ANTIBODY AGAINST VLA-4 INHIBITS EOSINOPHIL ACCUMULATION AND LATE ASTHMATIC RESPONSE IN A GUINEA-PIG MODEL OF ASTHMA
    SAGARA, H
    RA, C
    MATSUDA, H
    YAGITA, H
    OKUMURA, K
    FUKUDA, T
    MAKINO, S
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1994, 93 (01) : 269 - 269
  • [6] A monoclonal antibody against very late activation antigen-4 inhibits eosinophil accumulation and late asthmatic response in a guinea pig model of asthma
    Sagara, H
    Matsuda, H
    Wada, N
    Yagita, H
    Fukuda, T
    Okumura, K
    Makino, S
    Ra, C
    [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1997, 112 (03) : 287 - 294
  • [7] BLOCKADE OF BOTH IL-1A AND IL-1B BY A COMBINATION OF MONOCLONAL ANTIBODIES PREVENTS THE DEVELOPMENT AND REVERSES ESTABLISHED PAIN IN A PRECLINICAL MODEL OF OSTEOARTHRITIS
    Kamath, R. V.
    Simler, G.
    Zhou, C.
    Hart, M.
    Joshi, S.
    Ghayur, T.
    Honore, P.
    [J]. OSTEOARTHRITIS AND CARTILAGE, 2012, 20 : S62 - S62
  • [8] EVALUATION OF A MONOCLONAL ANTIBODY-BASED IMMUNOASSAY FOR DETECTING TYPE-B CLOSTRIDIUM-BOTULINUM TOXIN PRODUCED IN PURE CULTURE AND AN INOCULATED MODEL CURED MEAT SYSTEM
    GIBSON, AM
    MODI, NK
    ROBERTS, TA
    HAMBLETON, P
    MELLING, J
    [J]. JOURNAL OF APPLIED BACTERIOLOGY, 1988, 64 (04): : 285 - 291
  • [9] A Combination of Three Fully Human Toxin A- and Toxin B-Specific Monoclonal Antibodies Protects against Challenge with Highly Virulent Epidemic Strains of Clostridium difficile in the Hamster Model
    Anosova, Natalie G.
    Cole, Leah E.
    Li, Lu
    Zhang, Jinrong
    Brown, Anna M.
    Mundle, Sophia
    Zhang, Jianxin
    Ray, Satyajit
    Ma, Fuqin
    Garrone, Pierre
    Bertraminelli, Nicola
    Kleanthous, Harry
    Anderson, Stephen F.
    [J]. CLINICAL AND VACCINE IMMUNOLOGY, 2015, 22 (07) : 711 - 725
  • [10] Comparison of monovalent glycoprotein B with bivalent gB/pp65 (GP83) vaccine for congenital cytomegalovirus infection in a guinea pig model: Inclusion of GP83 reduces gB antibody response but both vaccine approaches provide equivalent protection against pup mortality
    Swanson, Elizabeth C.
    Gillis, Pete
    Hernandez-Alvarado, Nelmary
    Fernandez-Alarcon, Claudia
    Schmit, Megan
    Zabeli, Jason C.
    Wussow, Felix
    Diamond, Don J.
    Schleiss, Mark R.
    [J]. VACCINE, 2015, 33 (32) : 4013 - 4018