Effect of Plasma TNF-α on Filgrastim-Stimulated Hematopoiesis in Mice and Humans |
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Authors: | William P. Petros Pharm.D. FCCP Josh Rabinowitz B.S. John P. Gibbs B.S. Iris H. Hall Ph.D. Ann R. Stuart B.S. William P. Peters M.D. Ph.D. |
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Affiliation: | 1. Bone Marrow Transplant Program, Department of Medicine, Duke University Medical Center, Durham, North Carolina;2. Department of Medicinal Chemistry, School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina. |
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Abstract: | Study Objective . To delineate possible explanations for a nonmonotone hematopoiesis, dose-response curve with filgrastim therapy after high-dose chemotherapy. Design . Sequential two-phase study. Settings . University teaching hospital and basic pharmaceutical sciences laboratory. Subjects . Thirty-nine patients with breast cancer or melanoma and 15 normal CF-1 male mice. Interventions . Serial blood samples were obtained from patients after high-dose chemotherapy to evaluate hematopoiesis and tumor necrosis factor-α (TNF-α) concentrations. Murine hematopoiesis was induced by filgrastim with or without coadministration of lipopolysaccharide. Measurements and Main Results . Detection of plasma TNF-α in patients corresponded to substantially slower recovery of granulocytes, erythrocytes, and platelets, and was directly proportional to the prescribed dosage of filgrastim. Lipopolysaccharide stimulated the secretion of TNF-α in mice and totally aberrated filgrastim-induced granulopoiesis. Conclusions . This in vivo evidence suggests that regulatory pathways involving endogenous cytokines may override the effect of recombinant cytokines. |
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