Keratinocyte growth factor separates graft-versus-leukemia effects from graft-versus-host disease
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Krijanovski, OI
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机构:Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Krijanovski, OI
Hill, GR
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机构:Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Hill, GR
Cooke, KR
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机构:Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Cooke, KR
Teshima, T
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机构:Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Teshima, T
Crawford, JM
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机构:Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Crawford, JM
Brinson, YS
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机构:Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Brinson, YS
Ferrara, JLM
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Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USAUniv Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Ferrara, JLM
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机构:
[1] Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Ctr Canc, Div Hematol & Oncol, Dept Pediat, Ann Arbor, MI 48109 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Childrens Hosp, Dept Pediat Oncol, Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
The major obstacles to successful outcome after allogeneic bone marrow transplantation (BMT) for leukemia remain graft-versus-host disease (GVHD) and leukemic relapse. Improved survival after BMT therefore requires more effective GVHD prophylaxis that does not impair graft-versus-leukemia (GVL) effects, We studied the administration of human recombinant keratinocyte growth factor (KGF) in a well-characterized murine BMT model for its effects on GVHD. KGF administration from day -3 to +7 significantly reduced GVHD mortality and the severity of GVHD in the gastrointestinal(GI) tract, reducing serum lipopolysaccharide (LPS) and tumor necrosis factor (TNF)alpha levels, but preserving donor T-cell responses (cytotoxic T lymphocyte [CTL] activity, proliferation, and interleukin [IL]-2 production) to host antigens. When mice received lethal doses of P815 leukemia cells at the time of BMT, KGF treatment significantly decreased acute GVHD compared with control-treated allogeneic mice and resulted in a significantly improved leukemia-free survival (42% v 4%, P < .001). KGF administration thus offers a novel approach to the separation of GVL effects from GVHD. (C) 1999 by The American Society of Hematology.