Development of Hillchol®, a low-cost inactivated single strain Hikojima oral cholera vaccine

被引:12
|
作者
Sharma, Tarun [1 ]
Joshi, Neeraj [1 ]
Mandyal, Ashwani Kumar [1 ]
Nordqvist, Stefan L. [2 ]
Lebens, Michael [2 ]
Kanchan, Vibhu [1 ]
Lofstrand, Madeleine [2 ]
Jeverstam, Frida [2 ]
Ahasan, Mohammad Mainul [3 ]
Khan, Imran [3 ]
Karim, Mahbubul [3 ]
Muktadir, Hasneen [3 ]
Muktadir, Abdul [3 ]
Gill, Davinder [1 ]
Holmgren, Jan [2 ]
机构
[1] Jamia Hamdard, MSD Wellcome Trust Hilleman Labs Pvt Ltd, 2nd Floor Nanotechnol Bldg, New Delhi 110062, India
[2] Univ Gothenburg, Dept Microbiol & Immunol, Inst Biomed, Sahlgrenska Acad, Gothenburg, Sweden
[3] Incepta Vaccine Ltd, Dewan Idris Rd, Dhaka, Bangladesh
基金
英国惠康基金;
关键词
Vibrio cholerae; Oral cholera vaccine; Hikojima; Fermentation; Intestinal immunity; Vibriocidal antibodies; TOXIN-B-SUBUNIT; VIBRIO-CHOLERAE; IMMUNIZATION; FORMALDEHYDE; ASSAY;
D O I
10.1016/j.vaccine.2020.10.043
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cholera remains an important global health problem with up to 4 million cases and 140,000 deaths annually. Oral cholera vaccines (OCVs) are now a cornerstone of the WHOs "Ending Cholera - A Global Roadmap to 2030" global program for the eventual elimination of cholera. There are currently three WHO prequalified OCVs available, Dukoral (R), Shanchol (R) and Euvichol-Plus (R). These vaccines are effective but due to a multiple strain composition and two different methods of inactivation, are complex and costly to manufacture. We describe here the characterization and industrial scale development of Hillchol (R); a novel, likely affordable single-component OCV for low and middle-income countries. Hillchol (R) consists of formalin-inactivated bacteria of a stable recombinant Vibrio cholerae O1 El Tor Hikojima serotype strain expressing approximately 50% each of Ogawa and Inaba O1 LPS antigens. The novel OCV can be manufactured on an industrial scale at a low cost. Hillchol (R) was well tolerated in animal toxicology studies and shown to have non-inferior oral immunogenicity in mice for both intestinalmucosal and serological immune responses when compared with a WHO-prequalified OCV. The optimized production of this single component OCV will reduce cost of OCV production and thus substantially increase vaccine availability. Based on these results, Hillchol (R) has been produced at a GMP facility and used successfully for clinical phase I/II studies. (C) 2020 MSD Wellcome Trust Hilleman Laboratories Pvt Ltd. Published by Elsevier Ltd.
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页码:7998 / 8009
页数:12
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