Several recently completed trials have shown that acellular pertussis
vaccines induce substantial protection against pertussis. They are con
siderably less reactogenic than whole-cell vaccines and, as they consi
st of only one or a few purified proteins, they can be expected to cau
se less severe adverse events. The optimal composition of acellular va
ccines has not yet been determined. The number of vaccine antigens var
ies from one to five. All vaccines contain detoxified pertussis toxin.
Other antigens included in several vaccines are filamentous haemagglu
tinin, pertactin and fimbriae, but it remains to be proven that these
antigens contribute significantly to protection. Postlicensure studies
will be of importance in order to study possible rare adverse events
after acellular vaccines and to study the induction of herd immunity.