Cholera remains today a major health problem in most developing countries.
The long-term control of cholera depends on he improvement of hygiene but t
his is a distant goal for many countries. The availability of an effective
cholera vaccine is thus important for the prevention of cholera in such cou
ntries. More than a century after the first attempt to vaccinate against ch
olera by FERRAN in Spain, there is still no truly effective cholera vaccine
. A bacterial fraction vaccine, referred to as CH? + 2 was prepared by Prof
essor A. DODIN. A field trial of this vaccine was carried out in Zaire in 1
983. Significant protection was observed but this vaccine was not evaluated
in additional trials. Two other oral cholera vaccines, developed in Sweden
and in the USA, were widely experimented on human beings: a combination of
cholera toxin B-subunit and inactivated bacterial cells, and a live attenu
ated vaccine containing the genetically manipulated Vibrio cholerae O1 stra
in CVD 103-HgR. Despite their efficiency as evaluated in field trials (inac
tivated vaccine) or on volunteers (live vaccine), these vaccines have drawb
acks that may limit their usefulness as practical vaccines. Protection indu
ced by he inactivated vaccine was transient in young children, lasting only
approximately for six months. One of he safety concerns associated with li
ve vaccines is a possible reversion to virulence, Efforts should be continu
ed to find a better cholera vaccine. A new vaccine development program base
d upon rile hypothesis that immunoglobulin G directed to the O-specific pol
ysaccharide of Vibrio cholerae O1 could confer protective immunity to chole
ra. This program may lead to the development of a cholera conjugate vaccine
to elicit protection in infants.