GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR IN COMBINATION WITH PENTAVALENT ANTIMONY FOR THE TREATMENT OF VISCERAL LEISHMANIASIS

被引:12
|
作者
BADARO, R
NASCIMENTO, C
CARVALHO, JS
BADARO, F
RUSSO, D
HO, JL
REED, SG
JOHNSON, WD
JONES, TC
机构
[1] CORNELL UNIV MED COLL,DIV INTERNAL MED,ITHACA,NY
[2] SEATTLE BIOMED RES INST,SEATTLE,WA 98109
[3] SANDOZ PHARMA LTD,CLIN RES,CH-4002 BASEL,SWITZERLAND
关键词
D O I
10.1007/BF01973598
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The efficacy of GM-CSF was investigated in 20 neutropenic patients (< 1500 neutrophils/mu l) with acute visceral leishmaniasis due to Leishmania chagasi. Patients were randomized to receive either GM-CSF, 5 mu g/kg daily (intravenously or subcutaneously), or placebo for ten days, in combination with pentavalent antimony, 10-20 mg/kg daily for 20 days. Neutrophil counts mere significantly greater on days 5 and 10 of treatment in the GM-CSF group compared with the placebo group (p < 0.02). Eosinophil and monocyte counts were also significantly increased in the GM-CSF group at day 10 (p less than or equal to 0.03). Interestingly, at day 30, platelet counts were significantly higher in the GM-CSF treated group (p = 0.007). Haemoglobin levels were significantly increased in the GM-CSF group on days 5 and 10 (p = 0.04 and 0.02, respectively). Patients in the GM-CSF group experienced fewer secondary bacterial or viral infections than placebo patients. Infections occurred in only three patients given GMCSF compared with eight patients given placebo (p < 0.04). All patients had complete resolution of disease symptoms at three months. Few adverse events were recorded. GM-CSF given subcutaneously at a dose of 5 mu g/kg daily for ten days was well tolerated, reversed neutropenia rapidly and reduced the number of secondary infections in patients with leishmaniasis.
引用
收藏
页码:S23 / S28
页数:6
相关论文
共 50 条
  • [1] EFFECT OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR IN EXPERIMENTAL VISCERAL LEISHMANIASIS
    MURRAY, HW
    CERVIA, JS
    HARIPRASHAD, J
    TAYLOR, AP
    STOECKLE, MY
    HOCKMAN, H
    JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03): : 1183 - 1192
  • [2] Granulocyte colony-stimulating factor, granulocyte-macrophage colony-stimulating factor and macrophage colony-stimulating factor in the treatment of acute myeloid leukemia and acute lymphoblastic leukemia
    Ohno, R
    LEUKEMIA RESEARCH, 1998, 22 (12) : 1143 - 1154
  • [3] ROLE OF ENDOGENOUS GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR (GM-CSF) IN EXPERIMENTAL VISCERAL LEISHMANIASIS
    CERVIA, J
    HARIPRASHAD, J
    AGUERO, B
    YEGANEGI, H
    BOONE, T
    HOCKMAN, H
    MURRAY, HW
    CLINICAL RESEARCH, 1993, 41 (02): : A377 - A377
  • [4] GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR IN PSORIASIS
    TAKEMATSU, H
    TAGAMI, H
    DERMATOLOGICA, 1990, 181 (01): : 16 - 20
  • [5] GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR AND VASCULITIS
    DREICER, R
    SCHILLER, JH
    CARBONE, PP
    ANNALS OF INTERNAL MEDICINE, 1989, 111 (01) : 91 - 92
  • [6] MURINE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR
    BURGESS, AW
    NICE, EC
    METHODS IN ENZYMOLOGY, 1985, 116 : 588 - 600
  • [7] GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR AND PSORIASIS
    KELLY, RI
    MARSDEN, RA
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1994, 30 (01) : 144 - 144
  • [8] Functions of granulocyte-macrophage colony-stimulating factor
    Fleetwood, AJ
    Cook, AD
    Hamilton, JA
    CRITICAL REVIEWS IN IMMUNOLOGY, 2005, 25 (05) : 405 - 428
  • [9] GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR IN NEUTROPENIA
    HOGAN, KR
    PETERS, MD
    DICP-THE ANNALS OF PHARMACOTHERAPY, 1991, 25 (01): : 32 - 35
  • [10] HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR
    GASSON, JC
    NIMER, SD
    DIPERSIO, JF
    BALDWIN, GC
    WEISBART, RH
    GOLDE, DW
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1987, : 178 - 178