In vivo effects of recombinant human interleukin-6 in primates: stimulated production of platelets

S Asano(University of Tokyo Hospital), A Okano(University of Tokyo Hospital), Kazuhiro Ozawa(University of Tokyo Hospital), Tatsutoshi Nakahata(University of Tokyo Hospital), Toshihiro Ishibashi(University of Tokyo Hospital), Kazuhiko Koike(University of Tokyo Hospital), Hideo Kimura(University of Tokyo Hospital), Yoshikuni Tanioka(University of Tokyo Hospital), A Shibuya(University of Tokyo Hospital), Tomoko Hirano(University of Tokyo Hospital)
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Abstract

In cynomolgus monkeys, twice daily subcutaneous injections of recombinant human interleukin-6 (rhIL-6) at doses of 5 to 80 micrograms/kg/d for 14 consecutive days caused dose-dependent increases in platelet count, usually continuing for more than 1 week after cessation of the injections. The count reached a level approximately twofold or more above the preinjection level even at 5 micrograms/kg/d, and at doses of more than 20 micrograms/kg/d, the increase became biphasic with a higher second peak 3 days after cessation of the injections. Morphologic analysis of the bone marrow after the 7 day-injections with 80 micrograms/kg/d revealed a marked increment in size of megakaryocytes compared with control, indicating the promotion of megakaryocyte maturation. Other changes attributable to the rhIL-6 treatment include dose-dependent loss of body weight, anemia, neutrophilia and monocytosis, elevation of serum C-reactive protein and alpha-1 acid glycoprotein levels, and decrease of serum albumin; all of which returned to normal within 1 week after cessation of the injections and were tolerable at doses of less than 10 micrograms/kg/d. These findings suggest that rhIL-6 may be an effective strategy for the treatment of thrombocytopenia.


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