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

Bone Marrow Transplant. 2002 Oct;30(7):421-6. doi: 10.1038/sj.bmt.1703680.

Abstract

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.

MeSH terms

  • Adolescent
  • Antigens, CD / analysis
  • Antilymphocyte Serum / administration & dosage*
  • Antilymphocyte Serum / pharmacology
  • Child
  • Child, Preschool
  • Dose-Response Relationship, Drug
  • Drug Evaluation
  • Female
  • Graft Survival / drug effects
  • Graft Survival / immunology
  • Graft vs Host Disease / drug therapy
  • Graft vs Host Disease / prevention & control
  • Hematologic Neoplasms / mortality
  • Hematologic Neoplasms / therapy
  • Hematopoietic Stem Cell Transplantation / methods*
  • Hematopoietic Stem Cell Transplantation / mortality
  • Histocompatibility / immunology
  • Humans
  • Immune System / cytology
  • Immune System / drug effects*
  • Immune System / growth & development
  • Infant
  • Kinetics
  • Male
  • Opportunistic Infections
  • Retrospective Studies
  • Transplantation, Homologous

Substances

  • Antigens, CD
  • Antilymphocyte Serum