Today's most urgent problem in transplantation is the lack of suitable dono
r organs and tissues and as the population ages, demands for organs and tis
sue therapies will only increase. One alternative to organ transplantation
is cell therapy whose aim is to replace, repair or enhance the biological f
unction of damaged tissue or diseased organs. One goal of cellular transpla
ntation thus has been to find a renewable source of cells that could be use
d in humans. Embryonic stem (ES) cells have the potential to proliferate in
vitro in an undifferentiated and pluripotent state. Theoretically, ES cell
s are capable of unlimited proliferation in vitro. ES cells spontaneously d
ifferentiate into derivatives of all three primary germ layers: endoderm, e
ctoderm and mesoderm, hence providing cells in vitro which can theoreticall
y be isolated and used for transplantation. Furthermore, these pluripotent
stem cells can potentially be used to produce large numbers of cells that c
an be genetically modified in vitro. Once available, this source of cells m
ay obviate some of the critical needs for organ transplantation. Murine ES
cells have been extensively studied and all available evidence indicates th
at all aforementioned expectations are indeed fulfilled by ES cells. ES cel
ls as well as embryonic germ cells have recently been isolated and maintain
ed in culture. The recent descriptions of human ES cells portend the eventu
al use of allogeneic in vitro differentiated cells for human therapy. This
goal, however, is fraught with obstacles. Our aim is first to review the re
cent advances made with murine ES cells and then to point out potentials an
d difficulties associated with the use of human ES cells for transplantatio
n. Copyright (C) 1999 S. Karger AG, Basel.