부산대학교 도서관

BACKGROUND: The objective of this study was to establish a mobilization and apheresis regimen for collection of two consecutive polymorphonuclear neutrophil (PMN) concentrates from the same donor. STUDY DESIGN AND METHODS: In this prospective study, 111 healthy unrelated volunteers underwent either one (Group 1, n = 57) or two consecutive granulocyte apheresis procedure (Group 2, n = 54) using the a cell separator (Spectra). Both Group 1 and 2 donors were initially mobilized with glycosylated G-CSF 6.0 μg per kg (range, 5.2–7.0 μg/kg) subcutaneously plus oral dexa-methasone (DXM, 8 mg) and underwent granulocyte apheresis (GA-1) 16 hours (range, 13–18 hr) after initial G-CSF+DXM. Group 2 donors were remobilized with a second DXM dose of 8 mg (n = 13), 4 mg (n = 15), 1.5 mg (n = 13), or none (n = 13), and a second apheresis (GA-2) was run 40 hours (range, 37–42 hr) after G-CSF+DXM administration and 12 hours after remobilization with DXM alone. RESULTS: Based on equivalent median preapheresis WBC and PMN counts of around 35 × 10 WBCs per L and 33 × 10 PMNs per L after initial mobilization the GA-1 yields were 85 × 10 PMNs per U (range, 34–150) in Group 1 and 75 × 10 PMNs per U (range, 35–135) in Group 2 (p = 0.14, NS). In Group 2, median preapheresis values of 19.6 × 10 WBCs per L (range, 9.5–37.0) and 16.6 × 10 PMNs per L (range, 8.8–34.8) were measured after remobilization and GA-2 yields of 49 × 10 WBCs per U (range, 26–113) and 42 × 10 PMNs per U (range, 21–95) were obtained. Borderline statistical differences in the GA-2 yields were observed from the remobilized donors: 8 mg: 36 × 10 PMNs per U (range, 23–60); 4 mg: 47 × 10 PMNs per U (range, 21–56) (p ≤ 0.04); 1.5 mg: 45 × 10 PMNs per U (range, 23–79); placebo: 36 × 10 PMNs per U (range, 26–95) (p ≤ 0.04). CONCLUSION: Two consecutive neutrophil concentrates for transfusion can be obtained after single stimulation with Lenograstim+DXM. A second application of DXM alone is necessary, but of limited value.