Neutrophil defense in patients undergoing bone marrow transplantation: Bactericidal/permeability-increasing protein (BPI) and defensins in graft-derived neutrophils

被引:8
作者
Levy, O
Sisson, RB
Fryer, HE
Goldmann, D
Valore, E
Ganz, T
White, ML
Carroll, SF
Lehmann, L
Guinan, EC
机构
[1] Childrens Hosp, Div Infect Dis, Boston, MA 02115 USA
[2] Childrens Hosp, Gen Clin Res Ctr, Boston, MA 02115 USA
[3] Childrens Hosp, Dept Med, Div Med, Boston, MA 02115 USA
[4] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90024 USA
[5] XOMA US LLC, Dept Preclin Res, Berkeley, CA USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
D O I
10.1097/00007890-200205150-00027
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Background. Even after neutrophil counts return to near normal levels, patients undergoing myeloablative chemotherapy and bone marrow transplantation (BMT) are at risk for invasive bacterial infections, raising the possibility that their neutrophil function might be impaired. To assess potential qualitative defects in neutrophil function in patients undergoing BMT, we measured neutrophil content of the antimicrobial (poly)peptides BPI and defensins. Methods. Neutrophil extracts were analyzed for content of BPI by Western blotting and ELISA and for defensin peptides by acid-urea polyacrylamide gel electrophoresis (PAGE). Antibacterial activity of neutrophil extracts was measured against Escherichia coli K1/r, a clinical isolate sensitive to synergistic killing by BPI and defensins. Results. Neutrophil extract BPI content on post-BMT days +20, +30, and +100 (169+/-35, 232+/-57, and 160+/-55 ng per 10(6) neutrophils, respectively) was similar to the neutrophil BPI content of normal controls (163+/-35 ng per 10(6) neutrophils). Neutrophil defensin content also did not vary during this time-span. Activity of neutrophil extracts against E. coli K1/r did not differ between BAIT patients and controls. Conclusion. At post-BMT days +20 to +100, neutrophils derived from engrafted marrow contain normal quantities of BPI and defensins. Any deficiencies of neutrophil function during this phase are not due to inadequate expression of these antimicrobial (poly)peptides but could reflect abnormalities in other aspects of neutrophil function.
引用
收藏
页码:1522 / 1526
页数:5
相关论文
共 27 条
[1]
Recombinant granulocyte colony-stimulating factor induces production of human neutrophil peptides in lung cancer patients with neutropenia [J].
Ashitani, J ;
Nakazato, M ;
Mukae, H ;
Taniguchi, H ;
Date, Y ;
Matsukura, S .
REGULATORY PEPTIDES, 2000, 95 (1-3) :87-92
[2]
Granules of the human neutrophilic polymorphonuclear leukocyte [J].
Borregaard, N ;
Cowland, JB .
BLOOD, 1997, 89 (10) :3503-3521
[3]
CHASTY RC, 1993, BONE MARROW TRANSPL, V12, P331
[4]
Tumor necrosis factor-α production to lipopolysaccharide stimulation by donor cells predicts the severity of experimental acute graft-versus-host disease [J].
Cooke, KR ;
Hill, GR ;
Crawford, JM ;
Bungard, D ;
Brinson, YS ;
Delmonte, J ;
Ferrara, JLM .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (10) :1882-1891
[5]
Role of the bactericidal/permeability-increasing protein in host defence [J].
Elsbach, P ;
Weiss, J .
CURRENT OPINION IN IMMUNOLOGY, 1998, 10 (01) :45-49
[6]
Antibiotic peptides from higher eukaryotes: biology and applications [J].
Ganz, T ;
Lehrer, RI .
MOLECULAR MEDICINE TODAY, 1999, 5 (07) :292-297
[7]
HARWIG SSL, 1994, METHOD ENZYMOL, V236, P160
[8]
Antimicrobial peptides in mammalian and insect host defence [J].
Lehrer, RI ;
Ganz, T .
CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (01) :23-27
[9]
Prolonged but reversible neutrophil dysfunctions differentially sensitive to granulocyte colony-stimulating factor in children with acute lymphoblastic leukaemia [J].
Lejeune, M ;
Ferster, A ;
Cantinieaux, B ;
Sariban, E .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 102 (05) :1284-1291
[10]
Defective functional activity and accelerated apoptosis in neutrophils from children with cancer are differentially corrected by granulocyte and granulocyte-macrophage colony stimulating factors in vitro [J].
Lejeune, M ;
Cantinieaux, B ;
Harag, S ;
Ferster, A ;
Devalck, C ;
Sariban, E .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 106 (03) :756-761