Immune reconstitution after haematopoietic transplantation with two different doses of pre-graft antithymocyte globulin

被引:0
|
作者
M Duval
B Pédron
P Rohrlich
F Legrand
A Faye
B Lescoeur
P Bensaid
R Larchee
G Sterkers
E Vilmer
机构
[1] Service d'Hémato-immunologie,
[2] Hôpital Robert Debré,undefined
[3] Laboratoire d'Immunologie,undefined
[4] Hôpital Robert Debré,undefined
来源
Bone Marrow Transplantation | 2002年 / 30卷
关键词
allogeneic haematopoietic transplantation; unrelated donor; antithymocyte globulin; graft-versus-host disease; immune reconstitution;
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摘要
Antithymocyte globulin is widely used before haematopoietic transplantation with HLA-matched unrelated donors or mismatched relatives to prevent rejection and graft-versus-host disease (GVHD). However, optimal dosage is still under debate. Thirty-one consecutive children, mainly with haematological malignancies, were transplanted in a single institution with such donors, selected by HLA-A -B compatibility by serology and DRB1* by DNA typing. Antithymocyte globulin (Thymoglobuline; Sangstat) was infused at days −3, −2, −1. Total dosage varied: 16 patients received a median of 7.5 mg/kg (2.5 to 10.5: low-dose group), and 15 a median of 15.5 mg/kg (14.4 to 19.4: high-dose group). Post-transplant GVHD prophylaxis consisted of cyclosporine, short-course methotrexate and steroids. CD3+, CD4+ and CD19+ cell reconstitution was slower in the high-dose group. Median time to reach 100 CD4+ cells was 8 months vs 4 months (P = 0.03). Median time to normal CD19+ cells was 16 months vs 8 months (P = 0.01). CD16+CD56+ and CD8+ cell reconstitution was similar. Nine patients in the high-dose group and two in the low-dose group experienced life-threatening opportunistic infections (P = 0.009). Although obtained from a limited number of patients, our data suggest that a higher pre-graft dose of antithymocyte globulin may negatively influence immune reconstitution.
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页码:421 / 426
页数:5
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