Immunomagnetic CD4+ and CD8+ cell depletion for patients at high risk for severe acute GVHD

Bone Marrow Transplant. 1996 Mar;17(3):377-82.

Abstract

Acute GVHD remains a major problem in allogeneic BMT, in particular when donors other than HLA-identical siblings are used. To determine the efficacy of an immunomagnetic method for depletion of CD4+ and CD8+ lymphocytes from the marrow graft, a series of 15 patients was studied. Thirteen patients had matched unrelated donors, and two patients had related donors. Cyclosporine was used as GVHD prophylaxis in combination with CD4+ and CD8+ depletion, which removed 94.1 +/- 3.2%, 97.0 +/- 5.1%, and 96.7 +/- 3.1% of CD3+, CD4+ and CD8+ cells, respectively. All patients engrafted promptly with AGC > 500/mm3 after a median of 16 days post-BMT. Acute GVHD grade II-IV developed in 0/2 related transplants and 4/13 MUD transplants; only one patient had grade III-IV acute GVHD. No late graft failure was observed. Three patients relapsed; two had advanced disease at the time of BMT. Seven patients are alive and in CCR after a median of 497 days; actuarial survival is 39% at 24 months. The fever syndrome observed with selective CD8+ cell depletion was not seen with the combined CD4+ and CD8+ cell depletion. Immunomagnetic CD4+ and CD8+ cell depletion of marrow grafts, in combination with in vivo cyclosporine, is a simple, reproducible and effective method to decrease the incidence and severity of acute GVHD in patients at high risk for this complication after allogeneic BMT.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Acute Disease
  • Adolescent
  • Adult
  • Bone Marrow Transplantation / adverse effects*
  • Bone Marrow Transplantation / immunology
  • CD4 Lymphocyte Count*
  • CD8-Positive T-Lymphocytes*
  • Child
  • Child, Preschool
  • Cyclosporine / therapeutic use
  • Female
  • Fever / etiology
  • Graft vs Host Disease / epidemiology
  • Graft vs Host Disease / immunology*
  • Humans
  • Immunomagnetic Separation*
  • Incidence
  • Male
  • Middle Aged
  • Risk Factors
  • Syndrome
  • Transplantation, Homologous

Substances

  • Cyclosporine