A phase I/II study to evaluate safety, tolerability and immunogenicity of Hillchol®, an inactivated single Hikojima strain based oral cholera vaccine, in a sequentially age descending population in Bangladesh

被引:10
|
作者
Chowdhury, Fahima [1 ,2 ]
Syed, Khalid Ali [3 ]
Akter, Afroza [1 ]
Bhuiyan, Taufiqur Rahman [1 ]
Tauheed, Imam [1 ]
Khaton, Fatema [1 ]
Biswas, Rajib [1 ]
Ferdous, Jannatul [1 ]
Al Banna, Hasan [1 ]
Ross, Allen G. [1 ,2 ]
Mc Millan, Nigel [2 ]
Sharma, Tarun [3 ]
Kanchan, Vibhu [3 ]
Singh, Ajit Pal [3 ]
Gill, Davinder [3 ]
Lebens, Michael [4 ]
Nordqvist, Stefan [4 ]
Holmgren, Jan [4 ]
Clemens, John D. [1 ,5 ,6 ]
Qadri, Firdausi [1 ]
机构
[1] Int Ctr Diarrhoeal Dis Res Bangladesh Icddr B, 68 Shaheed Tajuddin Ahmed Sarani, Dhaka 1212, Bangladesh
[2] Menzies Hlth Inst Queensland, Gold Coast, Australia
[3] MSD Wellcome Trust Hilleman Labs, Delhi, India
[4] Univ Gothenburg, Gothenburg, Sweden
[5] Korea Univ Sch Med, Seoul, South Korea
[6] UCLA Fielding Sch Publ Hlth, Los Angeles, CA USA
基金
英国惠康基金;
关键词
Cholera; Vaccines; Hillchol (R); Hikojima; Clinical trial; Non-inferiority; IMMUNE-RESPONSES; BIVALENT; CHILDREN; ADULTS; TRIAL; O139;
D O I
10.1016/j.vaccine.2021.06.069
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The World Health Organization (WHO) recommends the use of oral cholera vaccines (OCVs) as part of an integrated control program, both in highly endemic settings and during cholera epidemics. The available and internationally recommended WHO-prequalified OCVs (Dukoral, Shanchol, Euvichol) contain multiple heat and formalin-killed V. cholerae strains of Inaba and Ogawa serotypes. MSD Wellcome Trust Hilleman Laboratories Pvt. Ltd. in technical collaboration with University of Gothenburg, Sweden has developed a new single strain OCV, Hillchol. This vaccine consists of formaldehyde-inactivated whole cell El Tor V. cholerae O1 bacteria engineered into the Hikojima serotype for stable expression of both the Ogawa (AB) and Inaba (AC) LPS antigens on the bacterial surface. We evaluated the safety and immunogenicity of this novel and potentially much less expensive OCV in comparison with Shanchol. Methods: We conducted a randomized, non-inferiority, age-descending clinical trial of OCV (Hillchol vs. Shanchol) in the Mirpur area of Dhaka city from July 2016 to May 2017. This study was carried out in three different age cohorts (1-<5, 5-17 and >18 years old). Two doses of vaccine were given at 14 days intervals to 560 healthy participants. Findings: No serious adverse events were reported. There were no significant differences in the rates of adverse events between the test vaccine (Hillchol) and the comparator (Shanchol) group. Serum vibriocidal antibody responses in all age groups combined were comparable for all the O1 Ogawa (59% vs. 67%; 90% CI of difference: -14.55, -0.84) and Inaba (70% vs. 71%; 90% CI of difference: -7.24, 5.77) serotypes, showing that the Hillchol vaccine was non-inferior to Shanchol. This new vaccine was also non-inferior to Shanchol in the different age strata. Conclusion: The safety and immunogenicity profile of the new OCV Hillchol is comparable to Shanchol in persons residing in a cholera-endemic setting. (C) 2021 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:4450 / 4457
页数:8
相关论文
共 34 条
  • [1] Development of Hillchol®, a low-cost inactivated single strain Hikojima oral cholera vaccine
    Sharma, Tarun
    Joshi, Neeraj
    Mandyal, Ashwani Kumar
    Nordqvist, Stefan L.
    Lebens, Michael
    Kanchan, Vibhu
    Lofstrand, Madeleine
    Jeverstam, Frida
    Ahasan, Mohammad Mainul
    Khan, Imran
    Karim, Mahbubul
    Muktadir, Hasneen
    Muktadir, Abdul
    Gill, Davinder
    Holmgren, Jan
    VACCINE, 2020, 38 (50) : 7998 - 8009
  • [2] A phase II, randomized, controlled trial to evaluate the safety and immunogenicity of a Sabin strain-based inactivated polio vaccine
    Tang, Rong
    Li, Guifan
    Zhang, Chengfu
    Zhi, Hengkui
    Zhu, Jiahong
    Wang, Jianjun
    Liang, Qi
    Hu, Yuemei
    Li, Changgui
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2020, 16 (11) : 2641 - 2648
  • [3] Immunogenicity and Safety of Inactivated Sabin-Strain Polio Vaccine "PoliovacSin": Clinical Trials Phase I and II
    Piniaeva, Anastasia
    Ignatyev, Georgy
    Kozlovskaya, Liubov
    Ivin, Yury
    Kovpak, Anastasia
    Ivanov, Alexander
    Shishova, Anna
    Antonova, Liliia
    Khapchaev, Yusuf
    Feldblium, Irina
    Ivanova, Olga
    Siniugina, Aleksandra
    Ishmukhametov, Aydar
    VACCINES, 2021, 9 (06)
  • [4] Safety, tolerability, and immunogenicity of an oral inactivated ETEC vaccine (ETVAX®) with dmLT adjuvant in healthy adults and children in Zambia: An age descending randomised, placebo-controlled trial
    Sukwa, Nsofwa
    Mubanga, Cynthia
    Hatyoka, Luiza M.
    Chilyabanyama, Obvious N.
    Chibuye, Mwelwa
    Mundia, Samson
    Munyinda, Masiliso
    Kamuti, Ethel
    Siyambango, Muyunda
    Badiozzaman, Sharif
    Bosomprah, Samuel
    Carlin, Nils
    Kaim, Joanna
    Sjostrand, Bjorn
    Simuyandi, Michelo
    Chilengi, Roma
    Svennerholm, Ann-Mari
    VACCINE, 2023, 41 (46) : 6884 - 6894
  • [5] Safety and immunogenicity of single-dose live oral cholera vaccine strain CVD 103-HgR in healthy adults age 18-45
    McCarty, James M.
    Lock, Michael D.
    Hunt, Kristin M.
    Simon, Jakub K.
    Gurwith, Marc
    VACCINE, 2018, 36 (06) : 833 - 840
  • [6] A double-blind, randomized controlled trial to evaluate the safety and immunogenicity of an intranasally administered trivalent inactivated influenza vaccine with the adjuvant LTh(αK): A phase II study
    Pan, Sung-Ching
    Hsu, Wei-Ting
    Lee, Wen-Sen
    Wang, Ning-Chi
    Chen, Tzeng-Ji
    Liu, Ming-Che
    Pai, Hui-Chen
    Hsu, Yu-Shen
    Chang, Mingi
    Hsieh, Szu-Min
    VACCINE, 2020, 38 (05) : 1048 - 1056
  • [7] Phase II, dose ranging study of the safety and immunogenicity of single dose West Nile vaccine in healthy adults ≥50 years of age
    Dayan, Gustavo H.
    Bevilacqua, Joan
    Coleman, Dorothy
    Buldo, Aileen
    Risi, George
    VACCINE, 2012, 30 (47) : 6656 - 6664
  • [8] Safety and immunogenicity of inactivated hepatitis-A vaccine developed by Human Biologicals Institute in two age groups of healthy subjects: A phase I open label study
    Susarla, Sai Krishna
    Palkar, Sonali
    Saradhi, Pardha S., V
    Diwan, Arundhati
    Barsode, Supriya
    Satish, M.
    Rajashakar, Bc
    Sandhya, G.
    Lingala, Rajendra
    Sahoo, Devi Prasad
    VACCINE, 2021, 39 (15) : 2088 - 2093
  • [9] A randomized Phase I/II study to evaluate safety and reactogenicity of a heat-stable rotavirus vaccine in healthy adults followed by evaluation of the safety, reactogenicity, and immunogenicity in infants
    Kanchan, Vibhu
    Zaman, Khalequ
    Aziz, Asma Binte
    Zaman, Sheikh Farzana
    Zaman, Farzana
    Haque, Warda
    Khanam, Mahbuba
    Karim, Mohammad Mahbubul
    Kale, Sachin
    Ali, Syed Khalid
    Goveia, Michelle G.
    Kaplan, Susan S.
    Gill, Davinder
    Khan, Wasif Ali
    Yunus, Mohammad
    Singh, Ajitpal
    Clemens, John D.
    HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2020, 16 (03) : 693 - 702
  • [10] Safety, reactogenicity and immunogenicity of a novel pneumococcal protein-based vaccine in adults: A phase I/II randomized clinical study
    Leroux-Roels, Geert
    Maes, Cathy
    De Boever, Fien
    Traskine, Magali
    Ruggeberg, Jens U.
    Borys, Dorota
    VACCINE, 2014, 32 (50) : 6838 - 6846