Low levels of mannose-binding lectin do not affect occurrence of severe infections or duration of fever in acute myeloid leukaemia during remission induction therapy

被引:65
作者
Bergmann, OJ
Christiansen, M
Laursen, I
Bang, P
Hansen, NE
Ellegaard, J
Koch, C
Andersen, V
机构
[1] Univ Copenhagen Hosp, Herlev Hosp, Dept Haematol, DK-2100 Copenhagen, Denmark
[2] Aarhus Univ Hosp, Dept Haematol, DK-8000 Aarhus, Denmark
[3] State Serum Inst, Copenhagen, Denmark
[4] Rigshosp, Inst Inflammat Res, DK-2100 Copenhagen, Denmark
关键词
mannose-binding lectin; acute myeloid leukaemia; granulocytopenia; septicaemia;
D O I
10.1034/j.1600-0609.2003.00012.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: To estimate the clinical significance of low serum concentrations of mannose-binding lectin (MBL) in patients with acute myeloid leukaemia (AML) during initial cancer chemotherapy. Patients and methods: 80 consecutive, newly diagnosed, and unselected AML patients (age 18-77 yr) undergoing remission induction chemotherapy. The patients were examined for 28 d. Main findings: Low levels of serum MBL (<1000 mu g/L) were found in 16/80 patients at diagnosis. This frequency is similar to what is found in the general population. In the remaining 64 patients, MBL concentrations were significantly higher than in controls and showed only a slight rise during the period of antineoplastic chemotherapy with its associated infectious complications. Low levels of MBL did not affect overall survival or morbidity in terms of incidence or duration of fever, or occurrence of septicaemia or pneumonia. Long-term survival was likewise independent of MBL concentration. Conclusion: MBL levels have no discernible influence on the occurrence or course of infections in AML patients during the initial hospitalisation. The predominant immunodeficiency during this phase is the profound granulocytopenia, which also compromises important effector functions of MBL. The finding in most AML patients of elevated MBL concentrations on admission is most likely because of the role of MBL as an acute phase reactant.
引用
收藏
页码:91 / 97
页数:7
相关论文
共 16 条
  • [1] ACYCLOVIR GIVEN AS PROPHYLAXIS AGAINST ORAL ULCERS IN ACUTE MYELOID-LEUKEMIA - RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL
    BERGMANN, OJ
    ELLERMANNERIKSEN, S
    MOGENSEN, SC
    ELLEGAARD, J
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 1995, 310 (6988): : 1169 - 1172
  • [2] ORAL INFECTIONS AND FEVER IN IMMUNOCOMPROMISED PATIENTS WITH HEMATOLOGIC MALIGNANCIES
    BERGMANN, OJ
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1989, 8 (03) : 207 - 213
  • [3] Acyclovir prophylaxis and fever during remission-induction therapy of patients with acute myeloid leukemia: A randomized, double-blind, placebo-controlled trial
    Bergmann, OJ
    Mogensen, SC
    EllermannEriksen, S
    Ellegaard, J
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (06) : 2269 - 2274
  • [4] QUANTITATIVE RELATIONSHIPS BETWEEN CIRCULATING LEUKOCYTES AND INFECTION IN PATIENTS WITH ACUTE LEUKEMIA
    BODEY, GP
    BUCKLEY, M
    SATHE, YS
    FREIREICH, EJ
    [J]. ANNALS OF INTERNAL MEDICINE, 1966, 64 (02) : 328 - +
  • [5] Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease
    Foster, CB
    Lehrnbecher, T
    Mol, F
    Steinberg, SM
    Venzon, DJ
    Walsh, TJ
    Noack, D
    Rae, J
    Winkelstein, JA
    Curnutte, JT
    Chanock, SJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (12) : 2146 - 2155
  • [6] Mannose-binding lectin: targeting the microbial world for complement attack and opsonophagocytosis
    Jack, DL
    Klein, NJ
    Turner, MW
    [J]. IMMUNOLOGICAL REVIEWS, 2001, 180 : 86 - 99
  • [7] Lipscombe R. J., 1992, Human Molecular Genetics, V1, P709, DOI 10.1093/hmg/1.9.709
  • [8] Prognostic factors in acute myeloid leukaemia
    Löwenberg, B
    [J]. BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2001, 14 (01) : 65 - 75
  • [9] MADSEN HO, 1995, J IMMUNOL, V155, P3013
  • [10] Mannose-binding lectin gene polymorphisms are associated with major infection following allogeneic hemopoietic stem cell transplantation
    Mullighan, CG
    Heatley, S
    Doherty, K
    Szabo, F
    Grigg, A
    Hughes, TP
    Schwarer, AP
    Szer, J
    Tait, BD
    To, LB
    Bardy, PG
    [J]. BLOOD, 2002, 99 (10) : 3524 - 3529