The complement-fixation test in the diagnosis of congenital toxoplasmosis
B. H. Kean and A. C. Kimball
We present serologic results on 26 patients with congenital toxoplasmosis
and on 22 of their mothers. The infection was severe (central nervous
system involvement) in 12 patients, 12 had only ocular manifestations, and
two were asymptomatic. The dye test results were positive on all specimens,
and were positive at a titer of 1:1,024 or higher if collected from
patients younger than 2 years of age. The complement-fixation test (CFT)
results were positive on all specimens from patients younger than 2 years
of age and on 69% of specimens collected from older patients. These
serologic results are contrasted with those obtained on two control groups:
(1) 46 uninfected infants followed up after birth because of substantial
antibody titers in their mothers during pregnancy; and (2) 190 infants and
children tested because toxoplasmosis was tentatively included in the
differential diagnosis of the current illness. In both control groups the
positive results on the CFT were limited almost exclusively to cord blood
specimens or specimens collected during the first 2 weeks of life. Lower
CFT titers in follow-up specimens suggested that the antibodies were
maternal in origin. These two tests are valuable in providing laboratory
support for the diagnosis of congenital toxoplasmosis, particularly the
test for the comparatively short-lived complement-fixing antibody.