Immune globulin are extracted from plasma pooled from 1000 or more don
ors. Each lot should contain at least 90 % of intact IgG. Intravenous
immune globulin are recommanded uenquivocally for some diseases: acute
autoimmune thrombocytopenic purpura of childhood, autoimmune erythrob
lastopenia, haemophilia with anti-VIII antibodies, Kawasaki's syndrome
, and perhaps, Guillain-Barre syndrome. Nevertheless, this therapy has
been reported to be beneficial for more than 35 diseases thought to b
e produced by immunopathology. Large amounts of immune globulin, such
as 400 to 2000 mg/kg are proposed over a period of two to five days. T
he safety of this treatment, which may be introduced without any speci
al structure, is a very interesting quality of the intravenous immune
globulin therapy. However, comparative efficacy against reference ther
apy, surveillance for long-term positive and adverse effects and cost-
effectiveness should be carried out.