Jm. Boiron et al., STABLE MIXED CHIMERISM WITHOUT RELAPSE AFTER RELATED ALLOGENEIC UMBILICAL-CORD BLOOD TRANSPLANTATION IN A CHILD WITH SEVERE APLASTIC-ANEMIA, Bone marrow transplantation, 22(8), 1998, pp. 819-821
Umbilical cord blood (UCB) cells from HLA-matched donors are used as a
n alternative to bone marrow for allogeneic transplantation and report
s of successful UCB transplantation in patients with severe aplastic a
nemia (SAA) are scarce. SAA was discovered in a 4-year-old girl in Feb
ruary 1990. Transfusion support started in August 1990 and standard tr
eatments were unsuccessful. The birth of an HLA-compatible brother in
October 1993 permitted the cryopreservation of UCB, In December 1994 U
CB transplantation was decided upon. No toxicity occurred. G-CSF was s
tarted at day 28, WBC and PMN reached 0.5 x 10(9)/1 at days 33 and 37,
RBC and platelet transfusion independence were reached at days 50 and
52, Mixed chimerism was demonstrated in blood cells at 1.5, 4 and 6 m
onths after UCBT by molecular biology (VNTR), FISH studies yielded sim
ilar results at 15 and 18 months, Twenty months after UCBT, molecular
biology showed full donor chimerism, Clinical follow-up (last follow-u
p: 32 months post transplant) is unremarkable, We suggest that CY and
ATG may be a suitable regimen for related HLA-compatible UCBT in patie
nts with SAA, Residual recipient cells can disappear even very late af
ter UCBT, permitting the establishment of complete donor chimerism.