The therapeutic efficacy of recombinant human leukemia inhibitory factor (LIF) was examined in a nonhuman primate model of radiation- induced marrow aplasia. Rhesus monkeys received 450 cGy of total-body, 1:1 mixed neutron:gamma radiation. For 23 days thereafter, each monkey received a daily subcutaneous injection of LIF or human serum albumin (HSA) at a dose of 15 micrograms/kg body weight. Complete blood counts and white blood cell differentials were monitored for 60 days postirradiation. Administration of LIF significantly decreased (P > or = .05) the duration of thrombocytopenia (platelet count > 30,000 or 20,000/microL), ie, 9.3 days or 6.3 days, respectively, versus the HSA- treated control monkeys, 12.2 days or 10.2 days, respectively. Treatment with LIF did not alter the duration of neutropenia (absolute neutrophil count > 1,000/microL) as compared with the HSA-treated control monkeys. Cytokine administration did not exacerbate the radiation-induced anemia observed in the HSA-treated control monkeys.
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December 1, 1994
Therapeutic efficacy of recombinant human leukemia inhibitory factor in a primate model of radiation-induced marrow aplasia
AM Farese,
AM Farese
Armed Forces Radiobiology, Research Institute, Bethesda, MD 20889-5603.
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LA Myers,
LA Myers
Armed Forces Radiobiology, Research Institute, Bethesda, MD 20889-5603.
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TJ MacVittie
TJ MacVittie
Armed Forces Radiobiology, Research Institute, Bethesda, MD 20889-5603.
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Blood (1994) 84 (11): 3675–3678.
Citation
AM Farese, LA Myers, TJ MacVittie; Therapeutic efficacy of recombinant human leukemia inhibitory factor in a primate model of radiation-induced marrow aplasia. Blood 1994; 84 (11): 3675–3678. doi: https://doi.org/10.1182/blood.V84.11.3675.bloodjournal84113675
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December 1 1994
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