Toxoplasmosis is a chronic, latent infection which can be reactivated
in the presence of immunosuppression. The critical question in obstetr
ics is whether toxoplasmosis may be reactivated in the presence of the
physiological ''immunosuppression'' of pregnancy. Standard in vitro t
ests, done in 24 healthy pregnant women and compared with the literatu
re, show no significant changes in humoral and cellular immunity durin
g pregnancy. However, the fact that some infections occur more frequen
tly and more severely than in non-pregnant women (e. g. those due to c
ytomegalovirus (CMV) and human papilloma virus (HPV) points to a degre
e of pregnancy-associated immunosuppression. Non-rejection of the semi
allogenic fetus is achieved in presence of maternal immunocompetence a
nd is explained mainly by local changes in immune function, mediated b
y inhibitors of decidual, placental and fetal origin, and by the absen
ce of class II histocompatibility antigens at the fetomaternal interfa
ce. Immune status allowing reactivation of toxoplasmosis was studied i
n a selected group of(predominantly male) AIDS patients from the Swiss
HIV Cohort study. Shortly before (cerebral) reactivation of toxoplasm
osis, 92% of these patients had very low CD4 lymphocyte counts (mean 5
0 cells/mu l, i. e. lower than ever recorded in a normal uncomplicated
pregnancy). In a larger population of 48 women receiving immunosuppre
ssive therapy after organ transplantation, not a single case of cerebr
al toxoplasmosis was observed during pregnancy, while in the 105 HIV-p
ositive women in the Swiss HIV and Pregnancy study, there was only one
case of cerebral toxoplasmosis during pregnancy and the puerperium (2
0 CD4/mu l), even though some 17% of those sampled (18/105) had CD4 le
vels below 200 cells/mu l on at least one occasion during pregnancy. T
hese findings explain why latent toxoplasmosis is not reactivated in n
ormal pregnancy, and why it is only likely in an immunosuppressed moth
er when her CD4 lymphocyte count is very low (< 200 cells/mu l). In su
ch cases, a prophylactic treatment to prevent maternal reactivation an
d vertical transmission of toxoplasmosis may be useful.