Neutrophils (PMNs) from patients with secondary iron overload have an incre
ased iron and ferritin content as well as a phagocytosis defect, Several se
rum components might be incriminated in the cellular iron accumulation, We
therefore compared the effects on the PMN phagocytosis of total serum as we
ll as the ferritin and transferrin fractions of serum derived from patients
with thalassemia major and healthy control subjects. An incubation system
of PMNs was developed, PMN phagocytosis was measured before and after incub
ation, Total serum from patients with thalassemia induced a defect that was
prevented by co-incubation with deferoxamine (DFO), Gel-filtration chromat
ography was performed to separate the serum fraction containing transferrin
and albumin from that containing ferritin, The transferrin-albumin fractio
n had no effect on PMN phagocytosis. On the contrary, the ferritin fraction
of normal serum was deleterious to PMN phagocytosis, and the same fraction
from thalassemic serum decreased PMN phagocytosis even more. Go-incubation
with DFO or catalase improved this defect, Moreover, a cellular increase i
n the L-type subunit of ferritin was observed after the incubation of PMNs
with the ferritin-containing fraction from thalassemic serum, In conclusion
, serum from patients with thalassemia is toxic to PMNs, and this toxicity
is due to ferritin-associated iron.