A non-inferiority trial comparing two killed, whole cell, oral cholera vaccines (Cholvax vs. Shanchol) in Dhaka, Bangladesh

被引:3
|
作者
Chowdhury, Fahima [1 ,2 ]
Akter, Afroza [1 ]
Bhuiyan, Taufiqur Rahman [1 ]
Tauheed, Imam [1 ]
Teshome, Samuel [3 ]
Sil, Arijit [3 ]
Park, Ju Yeon [3 ]
Chon, Yun [3 ]
Ferdous, Jannatul [1 ]
Basher, Salima Raiyan [1 ]
Ahmed, Faez [4 ]
Karim, Mahbubul
Ahasan, Mohammad Mainul [4 ]
Mia, Masudur Rahman [4 ]
Masud, Mir Mohammad Ibna [4 ]
Khan, Abdul Wahab [4 ]
Billah, Masum [4 ]
Nahar, Zebun [4 ]
Khan, Imran [4 ]
Ross, Allen G. [1 ,2 ]
Kim, Deok Ryun [3 ]
Ashik, Md. Muktadir Rahman [4 ]
Digilio, Laura [3 ]
Lynch, Julia [3 ]
Excler, Jean-Louis [3 ]
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] Int Vaccine Inst IVI, Seoul, South Korea
[4] Incepta Vaccine Ltd, Dhaka, Bangladesh
[5] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Los Angeles, CA USA
[6] Korea Univ, Sch Med, Seoul, South Korea
基金
比尔及梅琳达.盖茨基金会;
关键词
Cholera; OCV; Oral vaccines; Clinical trial; Non-inferiority; Cholvax; ANTIBODY-SECRETING CELL; MEMORY B-CELL; IMMUNE-RESPONSES; CHILDREN; ADULTS; O1; IMMUNOGENICITY; VACCINATION; FEATURES; SAFETY;
D O I
10.1016/j.vaccine.2021.12.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bangladesh remains cholera endemic with biannual seasonal peaks causing epidemics. At least 300,000 severe cases and over 4,500 deaths occur each year. The available oral cholera vaccines have not yet been adopted for cholera control in Bangladesh due to insufficient number of doses available for endemic control. With a public private partnership, icddr,b initiated a collaboration between vaccine manufacturers in Bangladesh and abroad. A locally manufactured Oral Cholera Vaccine (OCV) named Cholvax became available for testing in Bangladesh. We evaluated the safety and immunogenicity of this locally produced Cholvax (Incepta Vaccine Ltd) inexpensive OCV comparatively to Shanchol (Shantha Biotechnics-Sanofi Pasteur) which is licensed in several countries. We conducted a randomized non-inferiority clinical trial of bivalent, killed oral whole-cell cholera vaccine Cholvax vs. Shanchol in the cholera-endemic area of Mirpur, Dhaka, among three different age cohorts (1-5, 6-17 and 18-45 years) between April 2016 and April 2017. Two vaccine doses were given at 14 days apart to 2,052 healthy participants. No vaccine-related serious adverse events were reported. There were no significant differences in the frequency of solicited (7.31% vs. 6.73%) and unsolicited (1.46% vs. 1.07%) adverse events reported between the Cholvax and Shanchol groups. Vibriocidal antibody responses among the overall population for O1 Ogawa (81% vs. 77%) and O1 Inaba (83% vs. 84%) serotypes showed that Cholvax was non-inferior to Shanchol, with the non-inferiority margin of -10%. For O1 Inaba, GMT was 462.60 (Test group), 450.84 (Comparator group) with GMR 1.02(95% CI: 0.92, 1.13). For O1 Ogawa, GMT was 419.64 (Test group), 387.22 (Comparator group) with GMR 1.12 (95% CI: 1.02, 1.23). Cholvax was safe and non-inferior to Shanchol in terms of immunogenicity in the different age groups. These results support public use of Cholvax to contribute for reduction of the cholera burden in Bangladesh. ClinicalTrials.gov number: NCT027425581. (c) 2021 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:640 / 649
页数:10
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