scholarly journals Safety and immunogenicity in North Americans of a single dose of live oral cholera vaccine CVD 103-HgR: results of a randomized, placebo-controlled, double-blind crossover trial.

1992 ◽  
Vol 60 (10) ◽  
pp. 4430-4432 ◽  
Author(s):  
K L Kotloff ◽  
S S Wasserman ◽  
S O'Donnell ◽  
G A Losonsky ◽  
S J Cryz ◽  
...  
Author(s):  
James McCarty ◽  
Lisa Bedell ◽  
Paul-Andre de Lame ◽  
David Cassie ◽  
Michael Lock ◽  
...  

Vaccine ◽  
2018 ◽  
Vol 36 (6) ◽  
pp. 833-840 ◽  
Author(s):  
James M. McCarty ◽  
Michael D. Lock ◽  
Kristin M. Hunt ◽  
Jakub K. Simon ◽  
Marc Gurwith

2017 ◽  
Vol 16 (3) ◽  
pp. 197-213 ◽  
Author(s):  
Myron M. Levine ◽  
Wilbur H. Chen ◽  
James B. Kaper ◽  
Michael Lock ◽  
Lisa Danzig ◽  
...  

2002 ◽  
Vol 70 (4) ◽  
pp. 1965-1970 ◽  
Author(s):  
Mitchell B. Cohen ◽  
Ralph A. Giannella ◽  
Judy Bean ◽  
David N. Taylor ◽  
Susan Parker ◽  
...  

ABSTRACT Peru-15 is a live attenuated oral vaccine derived from a Vibrio cholerae O1 El Tor Inaba strain by a series of deletions and modifications, including deletion of the entire CT genetic element. Peru-15 is also a stable, motility-defective strain and is unable to recombine with homologous DNA. We wished to determine whether a single oral dose of Peru-15 was safe and immunogenic and whether it would provide significant protection against moderate and severe diarrhea in a randomized, double-blind, placebo-controlled human volunteer cholera challenge model. A total of 59 volunteers were randomly allocated to groups to receive either 2 × 108 CFU of reconstituted, lyophilized Peru-15 vaccine diluted in CeraVacx buffer or placebo (CeraVacx buffer alone). Approximately 3 months after vaccination, 36 of these volunteers were challenged with approximately 105 CFU of virulent V. cholerae O1 El Tor Inaba strain N16961, prepared from a standardized frozen inoculum. Among vaccinees, 98% showed at least a fourfold increase in vibriocidal antibody titers. After challenge, 5 (42%) of the 12 placebo recipients and none (0%) of the 24 vaccinees had moderate or severe diarrhea (≥3,000 g of diarrheal stool) (P = 0.002; protective efficacy, 100%; lower one-sided 95% confidence limit, 75%). A total of 7 (58%) of the 12 placebo recipients and 1 (4%) of the 24 vaccinees had any diarrhea (P < 0.001; protective efficacy, 93%; lower one-sided 95% confidence limit, 62%). The total number of diarrheal stools, weight of diarrheal stools, incidence of fever, and peak stool V. cholerae excretion among vaccinees were all significantly lower than in placebo recipients. Peru-15 is a well-tolerated and immunogenic oral cholera vaccine that affords protective efficacy against life-threatening cholera diarrhea in a human volunteer challenge model. This vaccine may therefore be a safe and effective tool to prevent cholera in travelers and is a strong candidate for further evaluation to prevent cholera in an area where cholera is endemic.


2013 ◽  
Vol 21 (1) ◽  
pp. 66-73 ◽  
Author(s):  
Wilbur H. Chen ◽  
Richard N. Greenberg ◽  
Marcela F. Pasetti ◽  
Sofie Livio ◽  
Michael Lock ◽  
...  

ABSTRACTCurrently, no cholera vaccine is available for persons traveling from the United States to areas of high cholera transmission and who for reasons of occupation or host factors are at increased risk for development of the disease. A single-dose oral cholera vaccine with a rapid onset of protection would be particularly useful for such travelers and might also be an adjunct control measure for cholera outbreaks. The attenuatedVibrio choleraeO1 vaccine strain CVD 103-HgR harbors a 94% deletion of the cholera toxin A subunit gene (ctxA) and has a mercury resistance gene inserted in the gene encoding hemolysin A. We undertook a phase I randomized placebo-controlled two-site trial to assess the safety and immunogenicity of a preliminary formulation of CVD 103-HgR prepared from new master and working cell banks. Healthy young adults were randomized (5:1 vaccinees to placebo recipients) to receive a single oral dose of ∼4.4 × 108CFU of vaccine or a placebo. Blood serum vibriocidal and cholera toxin-specific IgG antibodies were measured before and 10, 14, and 28 days following vaccination or placebo. Excretion of the vaccine strain in the stool was assessed during the first week postvaccination. A total of 66 subjects were enrolled, comprising 55 vaccinees and 11 placebo recipients. The vaccine was well tolerated. The overall vibriocidal and anti-cholera toxin seroconversion rates were 89% and 57%, respectively. CVD 103-HgR is undergoing renewed manufacture for licensure in the United States under the auspices of PaxVax. Our data mimic those from previous commercial formulations that elicited vibriocidal antibody seroconversion (a correlate of protection) in ∼90% of vaccinees. (This study has been registered at ClinicalTrials.gov under registration no. NCT01585181.)


2016 ◽  
Vol 375 (7) ◽  
pp. e12 ◽  
Author(s):  
Andrew S. Azman ◽  
Francisco J. Luquero

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