Infection with Toxoplasma gondii is the most common parasitic infectio
n worldwide with an estimated prevalence of 1-2 billion people. The ri
sk of developing severe toxoplasmosis is higher for immunocompromised
individuals and fetuses of mothers who have acquired a prime-infection
. The current therapy of choice for toxoplasmosis is the synergistic c
ombination of pyrimethamine and sulphadiazine. This therapy is highly
effective but its use is complicated in immuno-compromised individuals
due to adverse secondary effects. Ln addition, since pyrimethamine is
potentially teratogenic, its use is not recommended during early preg
nancy. Clindamycin, a lincosaminide, in combination with pyrimethamine
has been shown to be an acceptable therapeutic alternative in patient
s who are unable to tolerate pyrimethamine plus sulphadiazine. In the
search for new, effective compounds with less adverse or toxic effects
, recent efforts have focused on the new macrolides and the azalides.
Here, the results of the investigations and, in particular, the theore
tical considerations for the potential use of azithromycin in the ther
apy of toxoplasmosis in immunocompromised individuals are reviewed.