The effect of G-CSF-stimulated donor marrow on engraftment and incidence of graft-versus-host disease in allogeneic bone marrow transplantation

Graft-versus-host disease (GVHD) and infection are major obstacles to succe ssful allogeneic bone marrow transplantation (allo-BMT). In an attempt to i mprove the results of HLA-identical sibling BMT, we investigated the effect of accelerating hemopoietic reconstitution and reducing acute GVHD (aGVHD) in allo-BMT receiving G-CSF-stimulated donor marrow and the preliminary bi ological mechanism. The donors of 30 patients (study group) with leukemia w ere given G-CSF 3-4 mug/kg/d for 7 doses prior to marrow harvest. The resul ts of subsequent engraftment in the recipients were compared with those of 18 patients without G-CSF (control group). Five donors themselves were stud ied to assess the effects of G-CSF on the hematopoietic progenitor cells an d lymphocyte subsets in the bone marrow (BM). We observed that the stimulat ed BM yielded higher numbers of nucleated cells as well as CFU-GM and CD34( +) cells (p < 0.01), and that hemopoietic reconstitution was accelerated. T he median number of days of granulocyte count exceeding 0.5 x 10(9)/L and p latelet count exceeding 20 x 10(9)/L was 16 (range 10-23 d) and 18.5 (range 13-31 d), respectively (control group: median 22 d, range 13-29 d and medi an 23 d, range 17-34 d; p = 0.001). The incidence of grade II-IV severe aGV HD was very low, with only 1 case (3.3%) with acute grade II aGVHD limited to the skin in the study group. Five of 18 patients in the control group ma nifested grade II-IV severe aGVHD (27.8%, p = 0.02). The number of T-lympho cyte subsets in the harvested BM using G-CSF stimulation was changed. In th e G-CSF-stimulated marrow group, CD4(+) decreased and CD8(+) increased sign ificantly (p = 0.02). The changes of progenitor cells and T-lymphocyte subs ets in donors BM from pre- and post-G-CSF stimulation showed that the perce ntage of CD4(+) reduced (p = 0.04) and that of CD8(+) increased (p = 0.06), while that of CD34(+) also increased (p = 0.002). The incidence of chronic GVHD and relapse had no significant difference between both groups. These results indicate that allo-BMT in BM G-CSF priming can accelerate engraftme nt and minimize the incidence of severe aGVHD. There is a trend in favor of improved transplantation-related mortality.