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天花粉蛋白治疗HIV疾病的I/II期研究。

A phase I/II study of trichosanthin treatment of HIV disease.

作者信息

Byers V S, Levin A S, Waites L A, Starrett B A, Mayer R A, Clegg J A, Price M R, Robins R A, Delaney M, Baldwin R W

机构信息

University of Nottingham, UK.

出版信息

AIDS. 1990 Dec;4(12):1189-96. doi: 10.1097/00002030-199012000-00002.

Abstract

Trichosanthin, a ribosomal inhibitor protein, blocks HIV replication in lymphocytes and macrophages. This agent was used to treat 51 patients with advanced HIV disease in a dose-escalation study in which three injections were administered over a 9-21-day period in a dose range of 10-30 micrograms/kg per injection. The maximum tolerated dose was estimated to be 30 micrograms/kg. Reversible but severe fatigue and myalgias were the major dose-limiting side-effects; mild leucocytosis and elevations in serum transaminases were noted and were reversible. Non-dose-related reversible mental status changes were seen in six patients and were considered to be associated with the drug. This was usually manifest as dementia, but progressed to coma in two patients. This reversed, but the sequelae resulted in death in one patient. Decreases in serum p24 antigen levels were noted 1 month after the first infusion in 10 of 18 patients who entered the study with elevated levels; one converted to negative. Values usually remained low to the end of the study period (2 months). In those patients with CD4+ cell levels greater than 50 x 10(6) cells/l significant decreases in sedimentation rate and increases in CD4+ cell numbers were also noted. These changes were found at all dose levels but only in patients receiving three infusions.

摘要

天花粉蛋白是一种核糖体抑制蛋白,可阻断HIV在淋巴细胞和巨噬细胞中的复制。在一项剂量递增研究中,该药物被用于治疗51例晚期HIV疾病患者,在9至21天内分三次注射,每次注射剂量范围为10至30微克/千克。最大耐受剂量估计为30微克/千克。可逆但严重的疲劳和肌痛是主要的剂量限制性副作用;出现轻度白细胞增多和血清转氨酶升高,且这些情况是可逆的。6例患者出现与剂量无关的可逆性精神状态改变,认为与该药物有关。这通常表现为痴呆,但有2例进展为昏迷。这种情况有所逆转,但后遗症导致1例患者死亡。在18例入组时p24抗原水平升高的患者中,有10例在首次输注后1个月时血清p24抗原水平下降;1例转为阴性。这些值通常在研究期结束时(2个月)仍保持较低水平。在那些CD4+细胞水平大于50×10⁶个细胞/升的患者中,还观察到沉降率显著下降和CD4+细胞数量增加。这些变化在所有剂量水平都有发现,但仅见于接受三次输注的患者。

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