The presence of tumor-associated GD(3) in the plasma of 12 patients wi
th T-cell acute lymphoblastic leukemia (T-ALL) was determined utilizin
g microscale ganglioside isolation and thin layer chromatography (TLC)
immunodetection with an anti-GD(3) monoclonal antibody, R24. Immunost
aining of control plasma gangliosides revealed two nearly equal subspe
cies groups of GD(3), GD(3U) and GD(3L). Plasma from those T-ALL patie
nts with a high R24-positive lymphoblast count (>60 000/mm(3)) had a s
ignificant increase in total GD(3) and each of the GD(3) subspecies gr
oups, and a disproportionate increase in GD(3L) resulted in an increas
ed ratio GD(3L)/GD(3U) in these samples. In contrast, total GD(3), GD(
3) subspecies, and GD(3L)/GD(3U) was not increased in plasma from thos
e cases with low R24-positive blast count (<20 000/mm(3)) or in pre-B
ALL plasma. The altered GD(3) content in R24-positive T-ALL plasma was
reversible, since total GD(3) and GD(3L)/GD(3U) in plasma from a pati
ent in remission from R24-positive T-ALL was near that of controls. Re
sorcinol staining of TLC-separated gangliosides confirmed the results
observed with R24 detection methods. The results strongly suggest that
GD(3) is shed in vivo from T-ALL blasts in patients with R24-positive
T-ALL, resulting in both qualitative and quantitative changes in circ
ulating GD(3) in these