Proctor S J, Jackson G, Carey P, Stark A, Finney R, Saunders P, Summerfield G, Maharaj D, Youart A
Department of Haematology, Newcastle General Hospital, United Kingdom.
Blood. 1989 Nov 1;74(6):1894-7.
In 13 patients with severe steroid-refractory idiopathic immune thrombocytopenia (ITP), a short course of recombinant alpha 2b interferon (IFN), given at a dose of 3 MU for 12 doses, caused a significant increase in platelet count in 11 patients. The rise in platelet count occurred following completion of the short course of IFN in 10 patients and occurred during therapy in one patient. Three patients showed an increase to normal platelet counts within 14 days of discontinuing the drug, eight showed a partial response, with a platelet count increase from 30 to 100 x 10(9)/L, and two patients showed minimal response. One complete responder relapsed at 5 months from initial response, and a further course of alpha 2b IFN caused a second prompt response with a rise of platelet count to supranormal levels. Short-course alpha 2b IFN can be recommended as a therapy for severe ITP. Responses are seen in splenectomized and nonsplenectomized subjects, and thrombocytopenia is not exacerbated during treatment.
在13例严重的激素难治性特发性免疫性血小板减少症(ITP)患者中,给予一个疗程的重组α2b干扰素(IFN),剂量为3MU,共12剂,11例患者的血小板计数显著增加。10例患者在短疗程IFN治疗结束后血小板计数升高,1例患者在治疗期间血小板计数升高。3例患者在停药后14天内血小板计数升至正常,8例患者有部分反应,血小板计数从30升至100×10⁹/L,2例患者反应轻微。1例完全缓解者在初次缓解后5个月复发,再次给予α2b IFN疗程后血小板计数再次迅速升高至超正常水平。短疗程α2b IFN可推荐作为严重ITP的一种治疗方法。脾切除和未脾切除的患者均有反应,且治疗期间血小板减少症未加重。