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1.
PLoS One ; 3(6): e2323, 2008 Jun 04.
Article in English | MEDLINE | ID: mdl-18523643

ABSTRACT

OBJECTIVES: An effective vaccine against cholera has been used for public health purposes in Vietnam since the 1990s. This vaccine was reformulated to meet WHO requirements. We assessed the safety and immunogenicity of the reformulated bivalent (Vibrio cholerae 01 and 0139) killed whole cell oral vaccine in a cholera endemic area in Kolkata, India. DESIGN: Double-blind, randomized, placebo controlled trial. SETTING: The trial was conducted in the clinical trial ward of the Infectious Diseases Hospital in Kolkata, India. PARTICIPANTS: The participants were 101 healthy adults (males and non-pregnant females) aged 18-40 years and 100 healthy children (males and non-pregnant females) aged 1-17 years. INTERVENTIONS: Participants were randomized to receive either the bivalent killed whole cell oral cholera vaccine or placebo (killed oral Escherichia coli K12). OUTCOME MEASURES: For safety: proportion of subjects with adverse events during the duration of study participation. For immunogenicity: Proportion of subjects who had a > or = 4-fold rise in serum vibriocidal antibody titers 14 days after the second dose of vaccine or placebo. RESULTS: Adverse reactions were observed with similar frequency among vaccine and placebo recipients in both age groups. Among adults 4% of vaccine and 8% of placebo recipients and among children 4% of vaccine and 2% of placebo recipients had at least one adverse event within 28 days of the first dose of the vaccine. Following immunization, 53% of adult and 80% of children vaccinees showed a > or = 4 fold rise in serum V. cholerae O1 vibriocidal antibody titers. A less pronounced response to V. cholerae O139 vibriocidal antibody titers post-immunization was noted among vaccinees. CONCLUSIONS: We found the vaccine to be safe and immunogenic in a cholera-endemic area in India. TRIAL REGISTRATION: ClinicalTrials.gov NCT00119197.


Subject(s)
Cholera Vaccines/administration & dosage , Cholera/prevention & control , Endemic Diseases/prevention & control , Administration, Oral , Adolescent , Adult , Child , Child, Preschool , Cholera/epidemiology , Cholera/immunology , Cholera Vaccines/immunology , Double-Blind Method , Female , Humans , India/epidemiology , Infant , Male , Outcome Assessment, Health Care , Placebos , Sample Size
2.
Vaccine ; 25(6): 1149-55, 2007 Jan 22.
Article in English | MEDLINE | ID: mdl-17055622

ABSTRACT

Vietnam currently produces an orally administered, bivalent (O1 and O139) killed whole-cell vaccine and is the only country in the world with endemic cholera to use an oral cholera vaccine in public health practice. In order to allow international use, the vaccine had to be reformulated to meet World Health Organization (WHO) requirements. We performed a randomized, placebo controlled, safety and immunogenicity studies of this reformulated vaccine among Vietnamese adults. One hundred and forty-four subjects received the two-dose regimen and 143 had two blood samples obtained for analysis. We found that this reformulated oral killed whole-cell cholera vaccine was safe, well tolerated and highly immunogenic.


Subject(s)
Cholera Vaccines/administration & dosage , Cholera Vaccines/immunology , Cholera/immunology , Vibrio cholerae O139/immunology , Vibrio cholerae O1/immunology , Administration, Oral , Adolescent , Adult , Cholera/microbiology , Cholera/prevention & control , Cholera Vaccines/adverse effects , Double-Blind Method , Female , Humans , Male , Vaccines, Inactivated/administration & dosage , Vaccines, Inactivated/adverse effects , Vaccines, Inactivated/immunology , Vietnam
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