The passage of granulocyte-macrophage colony-stimulating factor across the human placenta perfused in vitro

被引:10
作者
Gregor, H
Egarter, C
Levin, D
Sternberger, B
Heinze, G
Leitich, H
Reisenberger, K
机构
[1] Univ Vienna, Dept Obstet & Gynecol, Sch Med, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Med Comp Sci, Sch Med, A-1090 Vienna, Austria
关键词
placental passage; granulocyte-macrophage colony-stimulating factor;
D O I
10.1016/S1071-5576(99)00042-8
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: The purpose of this study was to investigate the placental passage of granulocyte-macrophage colony-stimulating factor in a placental perfusion model ex vivo. METHODS: In an open system, 11 placentas were perfused on both the maternal and the fetal side immediately after delivery. Granulocyte-macrophage colony-stimulating factor was added to the maternal perfusion medium in concentrations from 10-55 mu g/mL. Maternal and fetal samples were taken, and granulocyte-macrophage colony-stimulating factor (GM-CSF) was measured by enzyme-linked immunosorbent assay. RESULTS: Accumulation of granulocyte-macrophage colony-stimulating factor in the fetal circuit averaged 2.42% of the concentration added initially to the arterial portion of the maternal circuit. CONCLUSION: There is only low transfer of GM-CSF across the fetal membranes. This finding is particularly remarkable in view of recently published results suggesting that administration of recombinant granulocyte growth factors to pregnant women with imminent preterm delivery helps prevent neonatal sepsis. (J Soc Gynecol Investig 1999;6:307-10) Copyright (C) 1999 by the Society for Gynecologic Investigation.
引用
收藏
页码:307 / 310
页数:4
相关论文
共 15 条
[1]   A NEW RECYCLING TECHNIQUE FOR HUMAN PLACENTAL COTYLEDON PERFUSION - APPLICATION TO STUDIES OF THE FETOMATERNAL TRANSFER OF GLUCOSE, INULIN, AND ANTIPYRINE [J].
BRANDES, JM ;
TAVOLONI, N ;
POTTER, BJ ;
SARKOZI, L ;
SHEPARD, MD ;
BERK, PD .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1983, 146 (07) :800-806
[2]   DECREASED STIMULATED GM-CSF PRODUCTION AND GM-CSF GENE-EXPRESSION BUT NORMAL NUMBERS OF GM-CSF RECEPTORS IN HUMAN TERM NEWBORNS COMPARED WITH ADULTS [J].
CAIRO, MS ;
SUEN, Y ;
KNOPPEL, E ;
VANDEVEN, C ;
NGUYEN, A ;
SENDER, L .
PEDIATRIC RESEARCH, 1991, 30 (04) :362-367
[3]  
CAIRO MS, 1992, J PEDIATR-US, V120, P281
[4]   RESULTS OF A PHASE I/II TRIAL OF RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR IN VERY-LOW-BIRTH-WEIGHT NEONATES - SIGNIFICANT INDUCTION OF CIRCULATORY NEUTROPHILS, MONOCYTES, PLATELETS, AND BONE-MARROW NEUTROPHILS [J].
CAIRO, MS ;
CHRISTENSEN, R ;
SENDER, LS ;
ELLIS, R ;
ROSENTHAL, J ;
VANDEVEN, C ;
WORCESTER, C ;
AGOSTI, JM .
BLOOD, 1995, 86 (07) :2509-2515
[5]   RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR PRIMES NEONATAL GRANULOCYTES FOR ENHANCED OXIDATIVE-METABOLISM AND CHEMOTAXIS [J].
CAIRO, MS ;
VANDEVEN, C ;
TOY, C ;
MAUSS, D ;
SENDER, L .
PEDIATRIC RESEARCH, 1989, 26 (05) :395-399
[6]   Transplacental passage of recombinant human granulocyte colony-stimulating factor in women with an imminent preterm delivery [J].
Calhoun, DA ;
Rosa, C ;
Christensen, RD .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1996, 174 (04) :1306-1311
[7]   EXHAUSTION OF MATURE MARROW NEUTROPHILS IN NEONATES WITH SEPSIS [J].
CHRISTENSEN, RD ;
ROTHSTEIN, G .
JOURNAL OF PEDIATRICS, 1980, 96 (02) :316-318
[8]   A CONTROLLED TRIAL OF INTRAVENOUS IMMUNE GLOBULIN TO REDUCE NOSOCOMIAL INFECTIONS IN VERY-LOW-BIRTH-WEIGHT INFANTS [J].
FANAROFF, AA ;
KORONES, SB ;
WRIGHT, LL ;
WRIGHT, EC ;
POLAND, RL ;
BAUER, CB ;
TYSON, JE ;
PHILIPS, JB ;
EDWARDS, W ;
LUCEY, JF ;
CATZ, CS ;
SHANKARAN, S ;
OH, W ;
CASSADY, G ;
BRAUNE, K ;
HACK, M ;
NEWMAN, NS ;
LITTLE, G ;
NATTIE, C ;
BAIN, RP ;
VERTER, J ;
YOUNES, N ;
HAWES, S ;
MURAN, G ;
BANDSTRA, ES ;
MARTINEZ, S ;
YAFFE, SJ ;
MALLOY, M ;
COOKE, R ;
MOORE, J ;
BURCHFIELD, J ;
HORBAR, JD ;
LEAHY, K .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (16) :1107-1113
[9]   NEUTROPHIL KINETICS IN ACUTE INFECTION [J].
MARSH, JC ;
BOGGS, DR ;
CARTWRIGHT, GE ;
WINTROBE, MM .
JOURNAL OF CLINICAL INVESTIGATION, 1967, 46 (12) :1943-+
[10]  
NOVALES JS, 1993, BLOOD, V81, P923