TY - JOUR
T1 - Circulating endothelial cells after transplantation ; author's reply
AU - Lagaaij, Emma Louise
AU - Van Kemenade, F.
AU - van Es, Bobo
AU - Bruijn, Jan Anthonie
AU - Van Krieken, Han
PY - 2001/5/5
Y1 - 2001/5/5
N2 - Sir,
The presence of recipient cells wasassociated with graft rejection, especially with vascular rejection. We speculated that bloodborne endothelial precursor cells could repair vascular damagecaused by rejection. Eberhard Gunsilius and colleagues suggest that the process we note in transplanted kidneys is similar to maintenance angiogenesis. We fully agree with this idea. Their data that bone-marrow-derived endothelial cells cause maintenance angiogenesis is in line with our hypothesis, that bloodborne cells lead to endothelial-cell chimerism. They propose that bloodborne endothelial cells, derived from the passenger leucocytes in the graft, home into the blood vessels outside the graft. This mechanism might result in a state of microchimerism.[...]Endothelial chimerism could, however, induce abnormal interactions between allogeneic cell types that could lead to endothelial-cell activation, cytokine secretion, and an inflammatory reaction resulting in endovasculitis and vascular rejection. We could not investigate whether the infiltrate precedes or follows endothelial chimerism, but this is an important issue that needs further investigation.
AB - Sir,
The presence of recipient cells wasassociated with graft rejection, especially with vascular rejection. We speculated that bloodborne endothelial precursor cells could repair vascular damagecaused by rejection. Eberhard Gunsilius and colleagues suggest that the process we note in transplanted kidneys is similar to maintenance angiogenesis. We fully agree with this idea. Their data that bone-marrow-derived endothelial cells cause maintenance angiogenesis is in line with our hypothesis, that bloodborne cells lead to endothelial-cell chimerism. They propose that bloodborne endothelial cells, derived from the passenger leucocytes in the graft, home into the blood vessels outside the graft. This mechanism might result in a state of microchimerism.[...]Endothelial chimerism could, however, induce abnormal interactions between allogeneic cell types that could lead to endothelial-cell activation, cytokine secretion, and an inflammatory reaction resulting in endovasculitis and vascular rejection. We could not investigate whether the infiltrate precedes or follows endothelial chimerism, but this is an important issue that needs further investigation.
UR - https://www.scopus.com/pages/publications/0035810588
U2 - 10.1016/S0140-6736(00)04606-7
DO - 10.1016/S0140-6736(00)04606-7
M3 - Comment/Letter to the editor
C2 - 11360955
AN - SCOPUS:0035810588
SN - 0140-6736
VL - 357
SP - 1449
EP - 1450
JO - Lancet
JF - Lancet
IS - 9266
ER -