T. Nagasawa et al., SIMULTANEOUS MEASUREMENTS OF MEGAKARYOCYTE-ASSOCIATED IGG (MAIGG) ANDPLATELET-ASSOCIATED IGG (PAIGG) IN CHRONIC IDIOPATHIC THROMBOCYTOPENIC PURPURA, European journal of haematology, 54(5), 1995, pp. 314-320
We have simultaneously measured platelet-associated IgG (PAIgG) and me
gakaryocyte-associated IgG (MAIgG) in 30 untreated patients with chron
ic idiopathic thrombocytopenic purpura (CITP). Megakaryocytes were pur
ified from bone marrow by 35% Percoll gradient centrifugation, followe
d by negative immunopanning using magnetic immunobeads. The normal ran
ge of MAIgG in 30 healthy donors was 15.5 +/- 10.0 ng/10(5) megakaryoc
ytes, whereas MAIgC in the 30 CITP patients was 140 +/- 59.3 ng/10(5)
megakaryocytes, although the values were widely distributed. From the
PaIgG and MAIgG data, CITP patients were classified into three types;
type I (PAIgG < 200 ng/10(7) platelets and MAIgG < 150 ng/10(5) megaka
ryocytes), type II (PAIgG > 200 ng and MAIgG > 150 ng), and type III (
PAIgC < 200 ng and MAlgG > 150 ng). Patients with types I and III had
good clinical courses, but, in contrast, patients with type II respond
ed poorly to steroid therapy followed by splenectomy or became refract
ory to treatment. In splenectomized patients. MAIgG of responder was p
romptly decreased to normal range and, in contrast, that of non-respon
der was persistently elevated. These results indicate that anti-platel
et autoantibodies are able to bind with megakaryocytes in the bone mar
row as well as with platelets in the peripheral blood, and the results
also suggest that megakaryopoiesis in CITP is heterogeneous. Simultan
eous measurement of PAIgG and MAIgG may predict the clinical outcome o
f CIPT.