THE alpha(+)-thalassaemias are the commonest known human genetic disor
ders, affecting up to 80 per cent of some populations(1). Although the
re is good evidence from both epidemiological(2,3) and clinical(4) stu
dies that these gene frequencies reflect selection by, and protection
from, malaria, the mechanism is unknown. We have studied the epidemiol
ogy of malaria in childhood on the southwestern Pacific island of Espi
ritu Santo in Vanuatu and here we report that, paradoxically, both the
incidence of uncomplicated malaria and the prevalence of splenomegaly
, an index of malaria infection, are significantly higher in young chi
ldren with alpha(+)-thalassnemia than in normal children. Furthermore,
this effect is most marked in the youngest children and for the nonle
thal parasite Plasmodium vivax. The alpha(+)-thalassaemias may have be
en selected for their ability beneficially to increase susceptibility
to P. vivax, which, by acting as a natural vaccine in this community,
induces limited cross-species protection against subsequent severe P.
falciparum malaria.