Investigations into the safety and immunogenicity of a killed oral cholera vaccine developed in Viet Nam

OBJECTIVE: To evaluate a killed oral cholera vaccine produced in Viet Nam, and to compare the Vietnamese vaccine with one that is licensed internationally. METHOD: Two-dose regimens of a locally produced, bivalent, anti-O1, anti-O139 killed oral whole-cell cholera vaccine (biv-WC) and of a commercia...

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Main Authors: Trach D.D (Author), Cam P.D (Author), Ke N.T (Author), Rao M.R (Author), Dinh D. (Author), Hang P.V (Author), Hung N.V (Author), Canh D.G (Author), Thiem V.D (Author), Naficy A. (Author), Ivanoff B. (Author), Svennerholm A-M (Author), Holmgren J. (Author), Clemens J.D (Author)
Format: Book
Published: The World Health Organization, 2002-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Trach D.D.  |e author 
700 1 0 |a Cam P.D.  |e author 
700 1 0 |a Ke N.T.  |e author 
700 1 0 |a Rao M.R.  |e author 
700 1 0 |a Dinh D.  |e author 
700 1 0 |a Hang P.V.  |e author 
700 1 0 |a Hung N.V.  |e author 
700 1 0 |a Canh D.G.  |e author 
700 1 0 |a Thiem V.D.  |e author 
700 1 0 |a Naficy A.  |e author 
700 1 0 |a Ivanoff B.  |e author 
700 1 0 |a Svennerholm A-M.  |e author 
700 1 0 |a Holmgren J.  |e author 
700 1 0 |a Clemens J.D.  |e author 
245 0 0 |a Investigations into the safety and immunogenicity of a killed oral cholera vaccine developed in Viet Nam 
260 |b The World Health Organization,   |c 2002-01-01T00:00:00Z. 
500 |a 0042-9686 
520 |a OBJECTIVE: To evaluate a killed oral cholera vaccine produced in Viet Nam, and to compare the Vietnamese vaccine with one that is licensed internationally. METHOD: Two-dose regimens of a locally produced, bivalent, anti-O1, anti-O139 killed oral whole-cell cholera vaccine (biv-WC) and of a commercially available, monovalent (anti-O1) oral recombinant B subunit-killed whole-cell cholera vaccine (rBS-WC) were compared in two trials in Viet Nam. In the first trial, 144 adults were randomized to biv-WC with or without buffer, rBS-WC with buffer, or placebo without buffer. In the second, 103 children aged 1-12 years were randomized to biv-WC without buffer, rBS-WC with buffer, or placebo without buffer. FINDINGS: No regimen was associated with significant side-effects. In adults, ca 60% of recipients of either vaccine exhibited at least fourfold serum anti-O1 vibriocidal antibody responses and ca 40% of recipients of biv-WC demonstrated anti-O139 vibriocidal responses. Both anti-O1 (ca 90% in each vaccine groupand anti-O139 (68% in the biv-WC group) vibriocidal responses occurred more frequently in children. The responses to biv-WC were unaffected by the receipt of buffer. CONCLUSION: It was concluded that biv-WC was safe and immunogenic, that it could be administered without buffer, and that it could elicit robust immune responses even in children, for whom the risk of endemic cholera is highest. 
546 |a EN 
690 |a Cholera vaccines/immunology 
690 |a Cholera vaccines/adverse effects 
690 |a Vaccines, Inactivated/immunology 
690 |a Vaccines, Inactivated/adverse effects 
690 |a Clinical trials 
690 |a Comparative study 
690 |a Viet Nam 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n Bulletin of the World Health Organization, Vol 80, Iss 1, Pp 2-8 (2002) 
787 0 |n http://www.scielosp.org/scielo.php?script=sci_arttext&pid=S0042-96862002000100003 
787 0 |n https://doaj.org/toc/0042-9686 
856 4 1 |u https://doaj.org/article/837f9049c66847aa81c1cf6eb977c340  |z Connect to this object online.