Korean J Hematol 1997; 32(2):

Published online June 30, 1997

© The Korean Society of Hematology

만성 골수증식성 질환 환자에서 혈청 Soluble Interleukin-2 Receptor치의 측정

이은엽, 조군제

부산대학교병원 임상병리과,
부산대학교 암연구소,
부산대학교병원 내과

Levels of Serum Soluble Interleukin-2 Receptor in Patients with Chronic Myeloproliferative Disorders

Eun Yup Lee, Goon Jae Cho

Department of Clinical Pathology, Internal Medicine, Pusan National University Hospital
Pusan Cancer Research Center, Pusan, Korea

Abstract

Background: A soluble form of interleukin-2 receptor(sIL-2R) is released from activated T cells. Serum sIL-2R levels are elevated in some hematological malignancies
and could be used to assess disease activity and prognosis.
Material and Methods: To define clinical usefulness and significance as a marker predicting disease progress in chronic myeloprolifsrative disorders, the serum levels of
sIL-2R were measured in 40 cases of chronic myelogenous leukemia(CML; 25 chronic phase, 7 accelerating phase, 8 blastic phase), 3 cases of polycythemia vera(PV), 5 cases
of essential thrombocythemia(ET) and 4 cases of idiopathic myelofibrosis(MF) and in 37 cases of healthy subjects using sandwich enzyme immunoassay.
Results: Serum sIL-2R levels in the patients of CML, PV, ET, and MF were higher compared with the normal healthy controls. In CML, serum sIL-2R levels in the patients
of blastic and accelerating phases were significantly higher than those of chronic phase. In CML of chronic phase, serum sIL-2R levels at diagnosis were related to WBC count but not to other clinical and hematologic paramaters. The leukemic cells of one patient with lymphoblastic phase of CML expressed IL-2R(CD25). Among 4 patients of CML with sIL-2R levels above 2,000U/mL at diagnosis, transformation to blastic crisis was noted in 3 patients and 2 patients died within 1 year after diagnosis. But among 11 patients of CML with sIL-2R levels below 2,000U/mL at diagnosis, only 2 patients experienced blastic crisis and died within 1 year after diagnosis.
Conclusion: This study indicated that serum sIL-2R levels were high in chronic myeloproliferative disorders, and that increasing levels of serum sIL-2R might be useful
to predict disease progress. Further studies including more patients and longer follow-up may substantiate serum sIL-2R as a prognostic indicator in CML.

Keywords Serum sIL-2R; Chronic myeloproliferative disorders; Chronic myelogenous leukemia;

Article

Korean J Hematol 1997; 32(2): 248-255

Published online June 30, 1997

Copyright © The Korean Society of Hematology.

만성 골수증식성 질환 환자에서 혈청 Soluble Interleukin-2 Receptor치의 측정

이은엽, 조군제

부산대학교병원 임상병리과,
부산대학교 암연구소,
부산대학교병원 내과

Levels of Serum Soluble Interleukin-2 Receptor in Patients with Chronic Myeloproliferative Disorders

Eun Yup Lee, Goon Jae Cho

Department of Clinical Pathology, Internal Medicine, Pusan National University Hospital
Pusan Cancer Research Center, Pusan, Korea

Abstract

Background: A soluble form of interleukin-2 receptor(sIL-2R) is released from activated T cells. Serum sIL-2R levels are elevated in some hematological malignancies
and could be used to assess disease activity and prognosis.
Material and Methods: To define clinical usefulness and significance as a marker predicting disease progress in chronic myeloprolifsrative disorders, the serum levels of
sIL-2R were measured in 40 cases of chronic myelogenous leukemia(CML; 25 chronic phase, 7 accelerating phase, 8 blastic phase), 3 cases of polycythemia vera(PV), 5 cases
of essential thrombocythemia(ET) and 4 cases of idiopathic myelofibrosis(MF) and in 37 cases of healthy subjects using sandwich enzyme immunoassay.
Results: Serum sIL-2R levels in the patients of CML, PV, ET, and MF were higher compared with the normal healthy controls. In CML, serum sIL-2R levels in the patients
of blastic and accelerating phases were significantly higher than those of chronic phase. In CML of chronic phase, serum sIL-2R levels at diagnosis were related to WBC count but not to other clinical and hematologic paramaters. The leukemic cells of one patient with lymphoblastic phase of CML expressed IL-2R(CD25). Among 4 patients of CML with sIL-2R levels above 2,000U/mL at diagnosis, transformation to blastic crisis was noted in 3 patients and 2 patients died within 1 year after diagnosis. But among 11 patients of CML with sIL-2R levels below 2,000U/mL at diagnosis, only 2 patients experienced blastic crisis and died within 1 year after diagnosis.
Conclusion: This study indicated that serum sIL-2R levels were high in chronic myeloproliferative disorders, and that increasing levels of serum sIL-2R might be useful
to predict disease progress. Further studies including more patients and longer follow-up may substantiate serum sIL-2R as a prognostic indicator in CML.

Keywords: Serum sIL-2R, Chronic myeloproliferative disorders, Chronic myelogenous leukemia,

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