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一项针对人免疫缺陷病毒1型gp120 V3环的嵌合鼠-人单克隆抗体的I/IIA期临床研究。

A phase I/IIA clinical study with a chimeric mouse-human monoclonal antibody to the V3 loop of human immunodeficiency virus type 1 gp120.

作者信息

Günthard H F, Gowland P L, Schüpbach J, Fung M S, Böni J, Liou R S, Chang N T, Grob P, Graepel P, Braun D G

机构信息

Department of Medicine, University Hospital of Zurich, Switzerland.

出版信息

J Infect Dis. 1994 Dec;170(6):1384-93. doi: 10.1093/infdis/170.6.1384.

Abstract

A phase I/IIA clinical trial with the chimeric mouse-human monoclonal antibody CGP 47,439 to the principal neutralization determinant in the V3 region of human immunodeficiency virus type 1 (HIV-1) strain IIIB envelope protein gp120 is reported. The trial was an uncontrolled single-center, open-label, multidose tolerability, immunogenicity, and pharmacokinetic study in homosexual men with advanced HIV disease. Patient groups were formed on the basis of the reactivity of the antibody with the gp120 of their HIV-1 isolates. Intravenous infusions of 1, 10, and 25 mg of antibody were followed by seven escalated doses of 50, 100, and 200 mg, every 3 weeks. The antibody was well tolerated; no toxicity was observed. Some patients showed a transient but insignificant antibody response to the antibody with no apparent adverse reactions or accelerated elimination of it. Substantial serum levels of the antibody were maintained with a mean t1/2 beta of 8-16 days. A virus burden reduction was observed in some patients.

摘要

报道了一项针对人免疫缺陷病毒1型(HIV-1)IIIB株包膜蛋白gp120 V3区主要中和决定簇的嵌合型鼠-人单克隆抗体CGP 47,439的I/IIA期临床试验。该试验是一项针对患有晚期HIV疾病的同性恋男性的非对照单中心、开放标签、多剂量耐受性、免疫原性和药代动力学研究。患者组是根据抗体与其HIV-1分离株的gp120的反应性形成的。静脉输注1、10和25mg抗体后,每3周给予7个递增剂量的50、100和200mg抗体。该抗体耐受性良好;未观察到毒性。一些患者对该抗体表现出短暂但不显著的抗体反应,没有明显的不良反应或抗体加速清除。抗体在血清中维持了较高水平,平均β半衰期为8-16天。在一些患者中观察到病毒载量降低。

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