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<strong>Parassitologia</strong> 50: 51-53, 2008<br />

Toxoplasmosis in pregnancy: evaluation of <strong>di</strong>agnostic<br />

methods<br />

V. Meroni, F. Genco<br />

Infectious Diseases Department University of Pavia, Foundation IRCCS Policlinico San Matteo Pavia<br />

Introduction<br />

Abstract. Toxoplasmosis in pregnancy is usually subclinic or associated with non specific symptoms.<br />

Diagnosis and timing of infection are usually based on serological tests. In this short review we tried to summarize<br />

the serological patterns we can encounter and to <strong>di</strong>scuss the interpretation of test results<br />

Toxoplasma gon<strong>di</strong>i is an obligate intracellular protozoan<br />

that infects almost a third of the world’s population.<br />

Primary infection with T. gon<strong>di</strong>i in pregnant<br />

women may result in congenital toxoplamosis via<br />

transplacental transmission. The extent of damage<br />

depends mainly on when the mother gets infected, with<br />

consequences being more severe during the early phases<br />

of gestation. However, transmission is more frequent<br />

during late pregnancy (Dunn et al., 1999).<br />

As parasitaemia lasts only few days and infection is<br />

often asymptomatic, the <strong>di</strong>agnosis relies mainly on<br />

serology (Montoya and Liesenfeld, 2004).<br />

Diagnosis of toxoplasmosis in pregnancy has two goals:<br />

to evaluate the immune status of the woman, and in<br />

case of acute infection, to date the time of infection. It<br />

is therefore advisable to perform serological tests<br />

before or at the beginning of pregnancy.<br />

Serological Tests<br />

Key words: toxoplasmosis in pregnancy, serological tests, prenatal <strong>di</strong>agnosis<br />

Given the kinetics of antibody production, the screening<br />

tests for toxoplasmosis are based on measurement<br />

of specific anti-Toxoplasma IgG and IgM antibo<strong>di</strong>es<br />

with automated tests, which usually have a good sensitivity<br />

and specificity.<br />

Anti–Toxoplasma IgG antibo<strong>di</strong>es are produced<br />

throughout life after infection. Detection in a single<br />

sample at any titre with any test is a marker of previous<br />

infection.<br />

IgM antibo<strong>di</strong>es are detected in recently acquired infections<br />

but may persist for more than a year. Furthermore<br />

false positive, aspecific reaction may be recorded in<br />

IgG negative patients.<br />

Four <strong>di</strong>fferent serological patterns may be seen<br />

(Montoya and Liesenfeld, 2004; Sensini 2006).<br />

Correspondence: Valeria Meroni<br />

Infectious Diseases Department University of Pavia,<br />

Foundation IRCCS Policlinico San Matteo Pavia,<br />

e-mail: v.meroni@smatteo.pv.it<br />

1-IgG negative IgM negative<br />

No immunity. Hygienic alimentary prophylaxis and<br />

monthly follow up (if possible until one month after<br />

delivery) in order to avoid seroconversion are advised.<br />

Indeed there is some evidence that health education<br />

may reduce the risk of seroconversion and consequently<br />

of congenital toxoplasmosis. (Gollub et al., 2008).<br />

In Italy, the screening test in pregnancy is not mandatory<br />

but National Health System pays for a preconceptional<br />

test and for the follow-up of negative women<br />

(DPR245 10/09/98) so most of pregnant women<br />

undergo the monthly controls.<br />

2-IgG positive IgM negative.<br />

Previous immunity, if the tests have been done before<br />

or at the beginning of pregnancy.<br />

No further sampling inclu<strong>di</strong>ng further pregnancies is<br />

required.<br />

In the third trimester, a negative IgM test cannot<br />

exclude an infection in the first trimester; in these cases<br />

it is necessary to perform other tests such as IgG avi<strong>di</strong>ty<br />

and further testing one month later to evaluate serological<br />

stability.<br />

3-IgG negative IgM positive.<br />

Early seroconversion or false positive result (Gussetti<br />

et al., 1990).<br />

In any seroconversion, IgG must must be produced, so<br />

it is mandatory to repeat a weekly sampling to detect<br />

IgG. If the patient has been treated, however, IgG production<br />

might be delayed and decreased. If this is the<br />

case, it is preferable to employ <strong>di</strong>fferent tests (IgG-IgM<br />

Immunoblot, cellular immunity tests ) to obtain a <strong>di</strong>agnosis<br />

as early as possible.<br />

If a seroconversion has been proved, by using ad<strong>di</strong>tional<br />

tests ,the clinician should prescribe the correct therapy.<br />

This also allows to advice the woman for prenatal<br />

<strong>di</strong>agnosis.<br />

If seroconversion is not confirmed ,treatment can be<br />

safely <strong>di</strong>scontinued..<br />

Immunoblot for IgG and IgM is a very specific test<br />

when purified antigens (not commercially available)<br />

are employed.<br />

The presence of 3 bands for IgG and two bands for IgM<br />

against 30-40 kD proteins can confirm seroconversion<br />

earlier than any other test (Sharma et al., 1983).

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