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接受生物反应调节剂治疗的晚期癌症患者缺乏针对细菌感染的保护作用。

Lack of protection against bacterial infections in patients with advanced cancer treated by biologic response modifiers.

作者信息

Maoleekoonpairoj S, Mittelman A, Savona S, Ahmed T, Puccio C, Gafney E, Skelos A, Arnold P, Coombe N, Baskind P

机构信息

Division of Neoplastic Diseases, New York Medical College, Valhalla 10595.

出版信息

J Clin Microbiol. 1989 Oct;27(10):2305-8. doi: 10.1128/jcm.27.10.2305-2308.1989.

Abstract

A survey of patients with advanced cancer treated by biologic response modifiers (BRMs), including (i) recombinant interleukin-2 and lymphokine-activated killer cells, (ii) recombinant interleukin-2 and alpha interferon, and (iii) tumor necrosis factor, was done. A total of 52 patients were reviewed. A total of 73 courses of BRMs were administered. Prior to the initiation of therapy, all patients were infection free and not receiving antibiotics. Twelve patients developed bacteremia during treatment with these BRMs. Five of these 12 patients had catheter-related bacteremia. Six patients had bacteremic infections without an obvious source, and one patient had a urinary tract infection with bacteremia. Staphylococcus epidermidis accounted for six of the isolates. Other organisms were Staphylococcus aureus, group B streptococci, viridans group streptococci, and gram-negative bacilli. This was an unexpectedly high incidence of bacterial infections in patients treated with BRMs. These BRMs have been previously shown to be efficacious against infections (by bacteria and other intracellular organisms) in experimental animals. In this study BRMs did not influence host defense mechanisms or offer protection against bacterial infections.

摘要

对接受生物反应调节剂(BRM)治疗的晚期癌症患者进行了一项调查,这些生物反应调节剂包括:(i)重组白细胞介素-2和淋巴因子激活的杀伤细胞;(ii)重组白细胞介素-2和α干扰素;以及(iii)肿瘤坏死因子。总共对52例患者进行了评估。共给予了73个疗程的BRM。在开始治疗前,所有患者均无感染且未接受抗生素治疗。12例患者在接受这些BRM治疗期间发生了菌血症。这12例患者中有5例发生了与导管相关的菌血症。6例患者发生了无明显来源的菌血症感染,1例患者发生了伴有菌血症的尿路感染。表皮葡萄球菌占分离出的病原体中的6例。其他病原体包括金黄色葡萄球菌、B组链球菌、草绿色链球菌和革兰氏阴性杆菌。在接受BRM治疗的患者中,细菌感染的发生率出乎意料地高。这些BRM此前已被证明在实验动物中对感染(由细菌和其他细胞内病原体引起)有效。在本研究中,BRM并未影响宿主防御机制,也未提供针对细菌感染的保护作用。

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