Neonatal lymphocytes dominate against lymphocytes of their own mother but not against allogenic maternal or adult lymphocytes in bidirectional mixed lymphocyte cultures

被引:3
作者
Brune, T
Beier, K
Exeler, R
Harms, E
Louwen, F
机构
[1] Univ Klinikum Magdeburg, Zentrum Kinderheilkunde, D-39112 Magdeburg, Germany
[2] Univ Munster, Dept Dermatol, D-4400 Munster, Germany
[3] Univ Munster, Dept Human Genet, D-4400 Munster, Germany
[4] Univ Munster, Dept Pediat, D-4400 Munster, Germany
[5] Goethe Univ Frankfurt, Dept Obstet & Gynecol, D-6000 Frankfurt, Germany
[6] Univ Magdeburg, Dept Pediat, D-39106 Magdeburg, Germany
关键词
leukocytes; pregnancy; adult; male; female; human; lymphocyte culture test; mixed; maternal-fetal; newborn;
D O I
10.1159/000069369
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Recent studies have shown a regular prenatal transfer of maternal immunocompetent cells into the fetal circulation. However, these cells engraft and proliferate only in a few exceptional cases if the fetus reaches an immunocompetent state. Thus the fetus has to have an immunologic defense mechanism against the engraftment of maternal cells. In the current study we investigated whether the fetus has such an immune defense and whether this defense mechanism specifically attacks cells of the mother. Patients, Material and Methods: Blood samples were obtained from 15 mothers and 15 newborns directly after delivery. We compared individual vitality and spontaneous cytotoxicity between fetal and maternal lymphocytes in a cell ratio of 1:1 in nonstimulated bidirectional mixed lymphocyte cultures (MLC). The distribution of each cell population within the MLC was visualized by fluorescence in situ hybridization and X/Y-DNA probes. This was compared to MLCs between unrelated fetal and maternal as well as between unrelated adult lymphocytes. Results: After 72 h, a significant cell shift was observed only in the MLC with neonatal lymphocytes mixed with cells of their own mother; there was a significantly higher number of neonatal cells (0.71 vs. 0.29) present. All other groups continued to have a cell distribution of 1:1. Conclusion: Our results show that neonatal lymphocytes specifically dominate against maternal but not allogenous maternal or adult lymphocytes in nonstimulated bidirectional MLCs. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:154 / 159
页数:6
相关论文
共 34 条
[1]   EXPRESSION OF HLA ANTIGENS, BETA-2-MICROGLOBULIN AND ENZYMES BY HUMAN AMNIOTIC EPITHELIAL-CELLS [J].
ADINOLFI, M ;
AKLE, CA ;
MCCOLL, I ;
FENSOM, AH ;
TANSLEY, L ;
CONNOLLY, P ;
HSI, BL ;
FAULK, WP ;
TRAVERS, P ;
BODMER, WF .
NATURE, 1982, 295 (5847) :325-327
[2]  
ADINOLFI M, 1976, LANCET, V1, P97
[3]  
APPLETON AL, 1994, BONE MARROW TRANSPL, V14, P157
[4]   Differentiation of single populations in a bidirectional mixed lymphocyte culture using X and Y chromosome-specific FISH markers [J].
Brune, T ;
Riepe, FG ;
Beier, K ;
Exeler, R ;
Louwen, F ;
Garritsen, H .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 266 (1-2) :105-110
[5]   Effect of pathological perinatal conditions on the maternofetal transfer of mononuclear cells [J].
Brune, T ;
Koch, HG ;
Plümpe, U ;
Coenen-Worch, V ;
Harms, E ;
Louwen, F .
FETAL DIAGNOSIS AND THERAPY, 2002, 17 (02) :110-114
[6]   Transplacental transmission of natural-killer-cell lymphoma [J].
Catlin, EA ;
Roberts, JD ;
Erana, R ;
Preffer, FI ;
Ferry, JA ;
Kelliher, AS ;
Atkins, L ;
Weinstein, HJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (02) :85-91
[7]   Ex vivo expansion of human umbilical cord blood does not lead to co-expansion of contaminating maternal mononuclear cells [J].
Fietz, T ;
Hilgenfeld, E ;
Berdel, WE ;
Hopp, H ;
Wenzel, U ;
Dohle, W ;
Thiel, E ;
Knauf, WU .
BONE MARROW TRANSPLANTATION, 1997, 20 (12) :1019-1026
[8]   ALLOGENEIC RESPONSES INVITRO INDUCED BY FETOMATERNAL ALLOIMMUNIZATION [J].
GENETET, N ;
GENETET, B ;
AMICE, V ;
FAUCHET, R .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1982, 2 (02) :90-96
[9]   SUPPRESSION OF LYMPHOCYTE-REACTIVITY INVITRO BY A SOLUBLE FACTOR SECRETED BY EXPLANTS OF HUMAN DECIDUA [J].
GOLANDER, A ;
ZAKUTH, V ;
SHECHTER, Y ;
SPIRER, Z .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1981, 11 (10) :849-851
[10]  
HERVA E, 1977, ACTA PATH MICRO IM C, V85, P333