Induced tolerance and chimaerism in human fetuses using coelocentesis: A medical opportunity to avert genetic disease?

被引:12
作者
Edwards, RG
Jauniaux, E
Binns, RM
Layton, M
Jurkovic, D
Grillo, TAI
Campbell, S
机构
[1] UNIV CAMBRIDGE CHURCHILL COLL,CAMBRIDGE,ENGLAND
[2] BABRAHAM INST,CAMBRIDGE,ENGLAND
[3] UNIV LONDON KINGS COLL,SCH MED,DEPT HAEMATOL MED,LONDON WC2R 2LS,ENGLAND
[4] UNIV LONDON KINGS COLL,SCH MED,DEPT OBSTET & GYNAECOL,EARLY HUMAN DEV UNIT,LONDON WC2R 2LS,ENGLAND
关键词
chimaerism; coelocentesis; embryo; human; inherited disease;
D O I
10.1093/humupd/1.4.419
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Coelocentesis offers a new opportunity for gaining access to the coelomic cavity of human embryos from 28 days post-fertilization (42 days menstrual age), With this technique, cells can be extracted from the cavity for the genetic typing of embryos in early pregnancy, Coelocentesis may also offer a unique opportunity of inducing tolerance to foreign grafts and chimaerism in these human embryos by replacing donor cells into the coelomic cavity, This cavity appears to be closely associated with the fetal haemopoietic system, The optimal age to inject stem cells designed to produce chimaerism may be at 5-6 weeks embryonic age, and these grafted cells may induce tolerance later in gestation, Two successive coelocenteses would be needed, the first to extract fetal cells to type the fetus, and a second within a few days to inject the donor cells into the coelomic cavity, Alternatively, non-invasive methods of diagnosis such as lower uterine pole extramembranous sampling of fetal trophoblast, or the extraction of fetal cells from maternal blood, could be combined with coelocentesis. If tolerance and chimaerism can be established, repeated tissue grafts could be carried out during fetal life and after birth, so that disorders caused by single or multiple gene defects in the haemopoietic system and other organs may be corrected.
引用
收藏
页码:419 / 427
页数:9
相关论文
共 70 条
[1]   DETECTION OF TRISOMY-18 AND Y-DERIVED SEQUENCES IN FETAL NUCLEATED CELLS OBTAINED BY TRANSCERVICAL FLUSHING [J].
ADINOLFI, M ;
DAVIES, A ;
SHARIF, S ;
SOOTHILL, P ;
RODECK, C .
LANCET, 1993, 342 (8868) :403-404
[2]   A SIMPLE ALTERNATIVE TO AMNIOCENTESIS [J].
ADINOLFI, M ;
SOOTHILL, P ;
RODECK, C .
PRENATAL DIAGNOSIS, 1994, 14 (03) :231-233
[3]   MULTIPLE LEVELS OF PERIPHERAL TOLERANCE [J].
ARNOLD, B ;
SCHONRICH, G ;
HAMMERLING, GJ .
IMMUNOLOGY TODAY, 1993, 14 (01) :12-14
[4]   MORPHOGENETIC INTERACTIONS IN THE DEVELOPMENT OF THE MOUSE THYMUS GLAND [J].
AUERBACH, R .
DEVELOPMENTAL BIOLOGY, 1960, 2 (03) :271-284
[5]   TECHNICAL ASPECTS OF INTRAVASCULAR INTRAUTERINE TRANSFUSIONS - LESSONS LEARNED FROM 33 PROCEDURES [J].
BERKOWITZ, RL ;
CHITKARA, U ;
WILKINS, I ;
LYNCH, L ;
MEHALEK, KE .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 157 (01) :4-9
[6]   ISOLATION OF FETAL DNA FROM NUCLEATED ERYTHROCYTES IN MATERNAL BLOOD [J].
BIANCHI, DW ;
FLINT, AF ;
PIZZIMENTI, MF ;
KNOLL, JHM ;
LATT, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (09) :3279-3283
[7]   ACTIVELY ACQUIRED TOLERANCE OF FOREIGN CELLS [J].
BILLINGHAM, RE ;
BRENT, L ;
MEDAWAR, PB .
NATURE, 1953, 172 (4379) :603-606
[8]   GENETIC-DISORDERS - METHODS OF AVOIDING THE BIRTH OF AN AFFECTED CHILD [J].
BRAMBATI, B .
HUMAN REPRODUCTION, 1993, 8 (11) :1983-2000
[9]   FAILURE OF EMBRYONIC MOUSE CELLS TO ENGRAFT IN IMMUNOCOMPETENT ALLOGENEIC RECIPIENTS [J].
BRENT, L ;
SHERWOOD, RA ;
LINCH, DC ;
GALE, RE .
BRITISH JOURNAL OF HAEMATOLOGY, 1990, 74 (04) :549-550
[10]   NON-SYNCYTIAL SOURCES OF FETAL DNA IN TRANSCERVICALLY RECOVERED CELL-POPULATIONS [J].
BRIGGS, J ;
MILLER, D ;
BULMER, JN ;
GRIFFITHJONES, M ;
RAME, V ;
LILFORD, R .
HUMAN REPRODUCTION, 1995, 10 (03) :749-754