A Japanese study to assess immunogenicity and safety of a typhoid Vi polysaccharide vaccine

被引:7
|
作者
Miyazu, Mitsunobu [1 ]
Kikuchi, Hitoshi [1 ]
Hamada, Atsuo [2 ]
Fukushima, Shinji [2 ]
Ouchi, Kazunobu [3 ]
Castells, Valerie Bosch [4 ]
Mihara, Hanako [5 ]
Bonnet, Marie-Claude [4 ]
机构
[1] Meitetsu Hosp, Nishi Ku, Nagoya, Aichi, Japan
[2] Tokyo Med Univ Hosp, Shinjuku Ku, Tokyo, Japan
[3] Kawasaki Med Sch, Kurashiki, Okayama, Japan
[4] Sanofi Pasteur, Marcy Letoile, France
[5] Sanofi KK, Tokyo, Japan
关键词
Typhoid; Vaccine; Japan; Safety; Immunogenicity; CAPSULAR POLYSACCHARIDE; SALMONELLA-TYPHI; FEVER; RESPONSES; TRIAL;
D O I
10.1016/j.vaccine.2015.10.086
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: Although typhoid fever is rare in Japan, imported cases have been reported occasionally in travelers returning from endemic areas. To achieve licensing of a typhoid Vi polysaccharide vaccine (Typhim Vi (R)) and make it widely available in Japan, this study was conducted at the request of the Japanese Ministry of Health Labor and Welfare to assess the immunogenicity and safety of this vaccine when given as a single dose (the recommended schedule of administration) in a Japanese population. Methods: In this multi-center, open-label, non-comparative, intervention study performed in Japan, 200 healthy volunteers (188 adults [>= 18 years of age], 7 adolescents [12-17 years of age] and 5 children 12-11 years of age]) were administered Typhim Vi (R). Immunogenicity was assessed 28 days after vaccinations using an ELISA method of anti-Vi antibody detection. A 4-fold increase in anti-Vi titer was considered as the threshold for seroconversion for anti-Vi antibodies. Safety was assessed up to 28 days following vaccination. Results: Overall, 92.0% (95% confidence interval [CI]: 87.3-95.4%) of participants achieved seroconversion 28 days after a single dose of typhoid Vi polysaccharide vaccine. GMTs of Vi antibody titers increased from 6.6 (95% CI: 5.8-7.4) prior to vaccination to 157.3 (95% CI: 135.1-183.2) on Day 28 after vaccination. The geometric mean of individual anti-Vi antibody titer ratios (Day 28/Day 0) was 23.9 (95% CI: 20.3-28.3). There were no immediate adverse events and no adverse events led to the discontinuation of participants from the study. Across all age groups, pain and myalgia were the most frequently reported injection site and systemic reactions, respectively. Most of these reactions were mild in intensity and resolved within 7 days. Conclusions: A single dose of typhoid Vi polysaccharide vaccine, Typhim Vi (R), demonstrated good safety and immunogenicity profile in a Japanese population. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:6697 / 6702
页数:6
相关论文
共 50 条
  • [22] Field effectiveness of Vi polysaccharide typhoid vaccine in the People's Republic of China
    Arya, SC
    JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (06): : 845 - 845
  • [23] A phase I clinical study to assess safety and immunogenicity of yellow fever vaccine
    Desai, Sajjad
    Anil, K.
    Potey, Anirudha Vyankatesh
    Sindhu, Y.
    Grappi, Silvia
    Lapini, Giulia
    Manney, Satyaprasad
    Tyagi, Parikshit
    Montomoli, Emanuele
    Poonawalla, Cyrus S.
    Kulkarni, Prasad S.
    NPJ VACCINES, 2022, 7 (01)
  • [24] Safety and immunogenicity of a Vi-DT typhoid conjugate vaccine: Phase I trial in Healthy Filipino adults and children
    Rosario Capeding, Maria
    Teshome, Samuel
    Saluja, Tarun
    Syed, Khalid Ali
    Kim, Deok Ryun
    Park, Ju Yeon
    Yang, Jae Seung
    Kim, Yang Hee
    Park, Jiwook
    Jo, Sue-Kyoung
    Chon, Yun
    Kothari, Sudeep
    Yang, Seon-Young
    Ham, Dong Soo
    Ryu, Ji Hwa
    Hwang, Hee-Seong
    Mun, Ju-Hwan
    Lynch, Julia A.
    Kim, Jerome H.
    Kim, Hun
    Excler, Jean-Louis
    Sahastrabuddhe, Sushant
    VACCINE, 2018, 36 (26) : 3794 - 3801
  • [25] Polysaccharide conjugate typhoid vaccine
    Guerrant, RL
    Kosek, M
    NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (17): : 1322 - 1323
  • [26] SAFETY, IMMUNOGENICITY, AND EFFICACY OF A BIVALENT CHOLERA-TYPHOID HYBRID VACCINE
    TACKET, CO
    FORREST, B
    LOSONSKY, G
    MORONA, R
    ATTRIDGE, SR
    LABROOY, J
    ROWLEY, D
    LEVINE, MM
    CLINICAL RESEARCH, 1989, 37 (02): : A442 - A442
  • [27] Safety and Immunogenicity of a Tetravalent Polysaccharide Vaccine Against Meningococcal Disease
    Shao, Pei-Lan
    Chang, Luan-Yin
    Hsieh, Szu-Min
    Chang, Shan-Chwen
    Pan, Sung-Ching
    Lu, Chun-Yi
    Hsieh, Yu-Chia
    Lee, Chin-Yun
    Dobbelaere, Kurt
    Boutriau, Dominique
    Tang, Haiwen
    Bock, Hans L.
    Huang, Li-Min
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2009, 108 (07) : 539 - 547
  • [28] An evaluation of the immunogenicity and safety of a new trivalent meningococcal polysaccharide vaccine
    Chandramohan, Daniel
    Hodgson, Abraham
    Coleman, Paul
    Baiden, Rita
    Asante, Kwaku
    Awine, Elizabeth
    Owusu-Agyei, Seth
    Boutriau, Dominique
    Nelson, Christopher B.
    Greenwood, Brain
    VACCINE, 2007, 25 : A83 - A91
  • [29] SAFETY AND IMMUNOGENICITY OF A POLYVALENT KLEBSIELLA CAPSULAR POLYSACCHARIDE VACCINE IN HUMANS
    CRYZ, SJ
    MORTIMER, P
    CROSS, AS
    FURER, E
    GERMANIER, R
    VACCINE, 1986, 4 (01) : 15 - 20
  • [30] Safety and immunogenicity of a new inactivated hepatitis A vaccine in concurrent administration with a typhoid fever vaccine or a typhoid fever plus yellow fever vaccine
    Dumas, R
    Forrat, R
    Lang, J
    Farinelli, T
    Loutan, L
    ADVANCES IN THERAPY, 1997, 14 (04) : 160 - 167