TY - JOUR
T1 - Cytomegalovirus infection following unrelated cord blood transplantation for adult patients
T2 - A single institute experience in Japan
AU - Tomonari, Akira
AU - Iseki, Tohru
AU - Ooi, Jun
AU - Takahashi, Satoshi
AU - Shindo, Motohiro
AU - Ishii, Koji
AU - Nagamura, Fumitaka
AU - Uchimaru, Kaoru
AU - Tani, Kenzaburo
AU - Tojo, Arinobu
AU - Asano, Shigetaka
PY - 2003/4
Y1 - 2003/4
N2 - Cytomegalovirus (CMV) infection in 28 adult patients after cord blood transplantation (CBT) from unrelated donors was compared with that after bone marrow transplantation from HLA (human leucocyte antigen)matched related (R-BMT) and unrelated (U-BMT) donors. Positive CMV antigenaemia was seen in 19 (79%) of 24 CMV-seropositive patients at a median of 42 d (range 29-85 d) after CBT, but in zero of four CMV-seronegative patients. This did not differ significantly from values observed after R-BMT and U-BMT (66%, P = 0.22, and 60%, P = 0.15 respectively). Based on the antigenaemia results, 16 patients (67%) received pre-emptive ganciclovir therapy from a median of 47 d (range 36-67 d) after CBT. This proportion was higher than that observed after R-BMT (28%. P = 0.0048), but did not differ from that after U-BMT (50%, P = 0.21). In addition, the probability of requiring more than two courses of ganciclovir therapy after CBT (21%) was higher than after R-BMT and U-BMT (0%. P = 0.015 and 0.039 respectively). One patient (5%) developed CMV disease after U-BMT, whereas no patients developed CMV disease after CBT or R-BMT. The CMV serostatus, use of a steroid and HLA disparity affected the probability of requiring ganciclovir therapy after CBT (P = 0.024, 0.032 and 0.017 respectively). These results suggest that recovery of CMV-specific immunity after CBT is delayed when compared with BMT.
AB - Cytomegalovirus (CMV) infection in 28 adult patients after cord blood transplantation (CBT) from unrelated donors was compared with that after bone marrow transplantation from HLA (human leucocyte antigen)matched related (R-BMT) and unrelated (U-BMT) donors. Positive CMV antigenaemia was seen in 19 (79%) of 24 CMV-seropositive patients at a median of 42 d (range 29-85 d) after CBT, but in zero of four CMV-seronegative patients. This did not differ significantly from values observed after R-BMT and U-BMT (66%, P = 0.22, and 60%, P = 0.15 respectively). Based on the antigenaemia results, 16 patients (67%) received pre-emptive ganciclovir therapy from a median of 47 d (range 36-67 d) after CBT. This proportion was higher than that observed after R-BMT (28%. P = 0.0048), but did not differ from that after U-BMT (50%, P = 0.21). In addition, the probability of requiring more than two courses of ganciclovir therapy after CBT (21%) was higher than after R-BMT and U-BMT (0%. P = 0.015 and 0.039 respectively). One patient (5%) developed CMV disease after U-BMT, whereas no patients developed CMV disease after CBT or R-BMT. The CMV serostatus, use of a steroid and HLA disparity affected the probability of requiring ganciclovir therapy after CBT (P = 0.024, 0.032 and 0.017 respectively). These results suggest that recovery of CMV-specific immunity after CBT is delayed when compared with BMT.
KW - Antigenaemia
KW - Cord blood transplantation
KW - Cytomegalovirus
KW - Ganciclovir
KW - Pre-emptive therapy
UR - https://www.scopus.com/pages/publications/0038555814
U2 - 10.1046/j.1365-2141.2003.04264.x
DO - 10.1046/j.1365-2141.2003.04264.x
M3 - 記事
C2 - 12694253
AN - SCOPUS:0038555814
SN - 0007-1048
VL - 121
SP - 304
EP - 311
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -