Tk. Mutabingwa et al., MALARIA CHEMOSUPPRESSION IN PREGNANCY .3. ITS EFFECTS ON THE MATERNALMALARIA IMMUNITY, Tropical and geographical medicine, 45(3), 1993, pp. 103-109
The malaria immune status of pregnant women participating in a malaria
prophylaxis study was assessed using their sera reactivity to the R32
tet32 antigen. Supervised prophylaxis started early in pregnancy till
delivery. Women randomly received either chloroquine once weekly (CQ),
or proguanil daily (PROG), or a combination of the two drugs (CQ+PROG
). Blood was collected at enrollment, then after 8, 16, and 24 weeks o
f prophylaxis. Of the 312 women who received prophylaxis for more than
10 consecutive weeks before delivery, anti-sporozoite antibodies were
assayed in 232 at enrollment, 258 after 8 weeks, and 254 after 16 wee
ks. Titres at enrollment were comparable by parity and the residential
area. Antibodies in women of the PROG group who were parasitaemic bef
ore the assessments decreased with the increasing number of breakthrou
gh and clinical episodes. The converse was true for antibodies in the
CQ and CQ+PROG groups. Group differences in the parasite densities wou
ld explain this. Parity and placental malaria did not influence titres
significantly. Overall, antibodies of the CQ+PROG group decreased sig
nificantly with time, possibly due to its long period of aparasitaemia
. This suggested interference with the immune responsiveness of the wo
men. PROG, which was equally efficacious, offers better prophylaxis.