± standard error; 545.2 ± ± ± ± 18.6 U/mL) rather than with lymphoma type ATL (327.62 ± ± ± ± 94.85 U/mL). In four patients whose sera were stored and examined longitudinally, the levels decreased following the response to chemotherapy but not in patients with chemotherapy resistance. Thus, our results imply that sCD30 levels may be another useful marker for the activity and aggressiveness of ATL. A dult T-cell leukemia/lymphoma (ATL) is a highly aggressive leukemia/ lymphoma which was first proposed as a new disease entity in 1977.(1,2) Subsequently, Shimoyama and the Lymphoma Study Group classified four clinical subtypes: acute type, lymphoma-type, chronic type, and smoldering type.(3) The long clinical latency and low incidence of ATL indicate that some genetic changes are involved in the malignant transformation and monoclonal expansion of human T-cell leukemia virus type 1 (HTLV-1)-infected cells. Monoclonal proliferation of HTLV-1-infected cells is observed in some virus carriers, who are considered to be the high risk group for development of ATL.(4) Constitutive activation of STAT proteins as well as the functional impairment and stabilization of p53 protein found in the peripheral blood mononuclear cells (PBMC) of ATL patients are supposed to be one base for ATL development.(5,6) However, it remains to be studied what the additional factors are that allow the monoclonal proliferation of ATL cells.CD30, a 120 kDa type I cell surface glycoprotein, is a member of the tumor necrosis factor receptor (TNFR) superfamily. The soluble form (sCD30) is produced by metalloprotease cleavage of the juxta-membrane region releasing as an extracellular region of 85 kDa protein. (7,8) CD30 is normally expressed by activated, but not by resting, B or T cells and also expressed on Hodgkin and Reed-Sternberg (H-RS) cells, anaplastic large cell lymphoma (ALCL) and ATL cells. (9) CD30 regulates their proliferation, differentiation and apoptotic cell death, depending on the cell type and developmental stage.(10) CD30 + cells release sCD30 in vitro and in vivo and it cannot be detected in the sera of healthy donors. (8,11) CD30 ligand (CD30L, CD153) is a type II transmembrane protein and a member of the TNF ligand superfamily.(12) It is expressed on resting B and activated T cells in addition to monocytes, granulocytes and natural killer cells.(7) Its pleiotropic biologic activities were reported, including its proliferative effect and CD30L-induced cell death. In ALCL and Hodgkin's disease (HD), elevated levels of sCD30 in the sera of patients are correlated with a poor prognosis, perhaps because a high level of sCD30 reflects a high tumor burden or because sCD30 blocks the biologic effects of CD30L.(15-17) Moreover, sCD30 is detectable in the sera of ATL patients. (11) In this study, we investigated the clinical significance of the membrane type of CD30 (mCD30) expression and serum sCD30 levels in ATL. Our results revealed the relationship between sCD30 levels and other serum markers of ATL.