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JG Kelton, CJ Carter, C Rodger, G Bebenek, J Gauldie, D Sheridan, YB Kassam, WF Kean, WW Buchanan and PJ Rooney
Platelet-associated IgG (PAIgG) has been reported to be elevated in
nonthrombocytopenic patients who have a normal platelet lifespan. This has
been interpreted as indicating that PAIgG is a nonspecific finding in these
patients and not a determinant of platelet survival. It is important to
recognize that the reticuloendothelial (RE) system plays an important role
in the clearance of antibody-sensitized cells. In this study, we related
the level of PAIgG and the platelet lifespan to the RE function in patients
with: (A) idiopathic thrombocytopenic purpura (ITP), and (B) five patients
with elevated levels of PAIgG yet normal or near-normal platelet counts. RE
function was assessed by measuring the clearance of autologous
chromium-labeled red cells sensitized with a precise amount of alloantibody
(2,000-3,600 molecules of IgG/cell). Eight patients with immune
thrombocytopenia had significantly shortened platelet survivals (less than
2-113 hr). In contrast, the five patients with elevated PAIgG, yet normal
or near- normal platelet counts, all had normal autologous platelet
survivals (186-222 hr). These patients also had significantly impaired
clearance of IgG-sensitized red cells, with an average of 85% of the
infused red cells remaining in the circulation at 60 min (normal 42% +/-
14%, n = 10). In this study, every patient with elevated PAIgG and normal
RE function had a shortened platelet lifespan. Those patients with elevated
PAIgG and impaired RE function did not invariably have a shortened platelet
lifespan. The observation that the PAIgG is elevated in some patients whose
platelet survival is normal does not indicate that PAIgG is not
biologically relevant. It indicates that these patients may have RE
blockade and do not clear IgG-sensitized cells.
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