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Published on: May 30, 2013
Prevention of travellers' diarrhoea by oral B-subunit/whole-cell cholera vaccine
H Peltola1, A Siitonen, H Kyrönseppä
1National Public Health Institute, Helsinki, Finland.
Insights
The B-subunit/whole-cell cholera vaccine (BS-WC) offers partial protection against travellers' diarrhoea. This oral vaccine demonstrated 52% efficacy against enterotoxigenic Escherichia coli (ETEC) infections in tourists.
Area of Science:
- Vaccinology
- Infectious Diseases
- Travel Medicine
Background:
- The B-subunit/whole-cell cholera vaccine (BS-WC) provides limited protection against enterotoxigenic Escherichia coli (ETEC) in Bangladeshi populations.
- Short-term protection is sufficient for preventing travellers' diarrhoea.
Purpose of the Study:
- To evaluate the efficacy of BS-WC in preventing travellers' diarrhoea among tourists traveling from Finland to Morocco.
Main Methods:
- A prospective, double-blind, placebo-controlled study was conducted with 615 tourists.
- Participants received either two oral doses of BS-WC or a placebo before travel.
- Faecal samples were collected and analyzed for enteropathogenic bacteria.
Main Results:
- Enteropathogenic bacteria were detected in 47% of symptomatic travellers and 14% of asymptomatic travellers.
- BS-WC provided 52% protection against ETEC-induced diarrhoea (p = 0.013).
- Higher protection rates were observed for mixed infections (65%) and combined infections including ETEC and other pathogens (71%–82%).
Conclusions:
- Active immunization with BS-WC can provide partial protection against travellers' diarrhoea.
- The vaccine is effective against ETEC and offers enhanced protection when combined with other pathogens.
Abstract:
B-subunit/whole-cell cholera vaccine (BS-WC) has been shown to give Bangladeshi mothers and children only 3 months' protection against severe diarrhoea due to enterotoxigenic Escherichia coli (ETEC). Since a long-lasting effect is not necessary for protection against travellers' diarrhoea, a prospective double-blind study was conducted among tourists who went to Morocco from Finland. 307 tourists received two oral doses of BS-WC, whereas 308 controls received a placebo before departure. A research team went out with tourists and a laboratory for enteric pathogens was set up on location. A faecal specimen was taken from 100 randomly selected subjects before departure, from all travellers with diarrhoea, and routinely after return. Enteropathogenic bacteria were not isolated from any of the pre-departure specimens but were present during or after the holiday in 47% of tourists with travellers' diarrhoea, and in 14% of those without diarrhoea. BS-WC induced a 52% protection (p = 0.013) against diarrhoea caused by ETEC. The protection was better for mixed infections (65%, p = 0.016). The protective efficacy against a combination of ETEC and any other pathogen was 71% (p = 0.02), and that against ETEC plus Salmonella enterica even better at 82% (p = 0.01). Partial protection against travellers' diarrhoea is thus obtainable by active immunisation with BS-WC.
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