CLINICAL PHARMACOKINETIC STUDIES OF A HUMAN HEMATOPOIETIC GROWTH-FACTOR, GM-CSF

被引:33
|
作者
HOVGAARD, D
MORTENSEN, BT
SCHIFTER, S
NISSEN, NI
机构
[1] UNIV COPENHAGEN HOSP,RIGSHOSP,DEPT HEMATOL,DK-2100 COPENHAGEN,DENMARK
[2] UNIV COPENHAGEN HOSP,RIGSHOSP,DEPT CLIN PHYSIOL & NUCL MED,DK-2100 COPENHAGEN,DENMARK
关键词
GM-CSF; HEMATOPOIETIC GROWTH FACTOR; PHARMACOKINETICS;
D O I
10.1111/j.1365-2362.1992.tb01934.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The pharmacokinetics of glycosylated recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) was studied following intravenous (i.v.) and subcutaneous (s.c.) bolus injection of rhGM-CSF, 8-mu-g kg-1 employing a sensitive radioimmunoassay. After a single i.v. bolus injection, an initial high serum level of rhGM-CSF was observed, followed by a rapid decrease that occurred in two phases with a half-life (t1/2) alpha of 20.0 +/- 5 min and a t1/2 beta of 68.3 +/- 8 min. Following s.c. bolus injection the absorption was more prolonged. Peak serum concentrations did not occur until about 15-20 h, and were followed by a more protracted elimination than by the i.v. route. In all patients the single rhGM-CSF injection led to an increase in peripheral white blood cells (WBC), after a temporary drop of 2-5 h duration. The increase in WBC was of longer duration after s.c. than after i.v. bolus treatment. Since the subcutaneous administration leads to prolonged serum concentration of rhGM-CSF and prolonged increase in peripheral WBC, it seems preferable to i.v. bolus injection, and as effective as continuous i.v. infusion.
引用
收藏
页码:45 / 49
页数:5
相关论文
共 50 条
  • [31] The granulocyte macrophage colony stimulating factor (GM-CSF) regulates amyloid β (Aβ) production
    Volmar, Claude-Henry
    Ait-Ghezala, Ghania
    Frieling, Jeremy
    Paris, Daniel
    Mullan, Michael J.
    CYTOKINE, 2008, 42 (03) : 336 - 344
  • [32] Comparative studies of the effects of recombinant GM-CSF and GM-CSF administered via a poxvirus to enhance the concentration of antigen-presenting cells in regional lymph nodes
    Kass, E
    Parker, J
    Schlom, J
    Greiner, JW
    CYTOKINE, 2000, 12 (07) : 960 - 971
  • [33] RECONSTITUTION OF FUNCTIONAL RECEPTORS FOR HUMAN GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR (GM-CSF) - EVIDENCE THAT THE PROTEIN ENCODED BY THE AIC2B CDNA IS A SUBUNIT OF THE MURINE GM-CSF RECEPTOR
    KITAMURA, T
    HAYASHIDA, K
    SAKAMAKI, K
    YOKOTA, T
    ARAI, K
    MIYAJIMA, A
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (12) : 5082 - 5086
  • [34] GM-CSF downmodulates c-kit, FcεRIα and GM-CSF receptor expression as well as histamine and tryptase levels in cultured human mast cells
    Welker, P
    Grabbe, J
    Zuberbier, T
    Grützkau, A
    Henz, BM
    ARCHIVES OF DERMATOLOGICAL RESEARCH, 2001, 293 (05) : 249 - 258
  • [35] The effect of uteroferrin and recombinant GM-CSF on hematopoietic parameters in normal female pigs (Sus scrofa)
    Laurenz, JC
    Hadjisavas, M
    Schuster, D
    Bazer, FW
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1997, 118 (03): : 579 - 586
  • [36] AGE-DEPENDENT ALTERATIONS OF HUMAN RECOMBINANT GM-CSF EFFECTS ON HUMAN GRANULOCYTES
    SERES, I
    CSONGOR, J
    MOHACSI, A
    LEOVEY, A
    FULOP, T
    MECHANISMS OF AGEING AND DEVELOPMENT, 1993, 71 (1-2) : 143 - 154
  • [37] THE APPLICATION OF G-CSF AND GM-CSF AS AN ADJUNCT TO CHEMOTHERAPY IN CLINICAL-PRACTICE - PERSPECTIVES AND CHALLENGES
    GREIL, R
    ONKOLOGIE, 1993, 16 (05): : 310 - 328
  • [38] Tumor necrosis factor administration is associated with increased endogenous production of M-CSF and G-CSF hut not GM-CSF in human cancer patients
    Logan, TF
    Gooding, W
    Kirkwood, JM
    Shadduck, RK
    EXPERIMENTAL HEMATOLOGY, 1996, 24 (01) : 49 - 53
  • [39] GM-CSF and ipilimumab therapy in metastatic melanoma: Clinical outcomes and immunologic responses
    Kwek, Serena S.
    Kahn, James
    Greaney, Samantha K.
    Lewis, Jera
    Cha, Edward
    Zhang, Li
    Weber, Robert W.
    Leonard, Lonnie
    Markovic, Svetomir N.
    Fong, Lawrence
    Spitler, Lynn E.
    ONCOIMMUNOLOGY, 2016, 5 (04):
  • [40] Therapeutical uses of haematopoietic growth factors. II. GM-CSF and G-CSF
    Royer, B
    Arock, M
    ANNALES DE BIOLOGIE CLINIQUE, 1998, 56 (03) : 255 - 266