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用抗γ-干扰素单克隆抗体预处理的两阶段重度联合免疫缺陷小鼠模型用于抗微小隐孢子虫药物测试的评估。

Evaluation of a two-phase scid mouse model preconditioned with anti-interferon-gamma monoclonal antibody for drug testing against Cryptosporidium parvum.

作者信息

Tzipori S, Rand W, Theodos C

机构信息

Department of Comparative Medicine, Tufts University School of Veterinary Medicine, Grafton, MA 01536, USA.

出版信息

J Infect Dis. 1995 Oct;172(4):1160-4. doi: 10.1093/infdis/172.4.1160.

Abstract

One 1-mg injection of anti-interferon-gamma monoclonal antibody (anti-IFN-gamma MAb) into newly weaned scid mice 2 h before challenge with Cryptosporidium parvum oocysts markedly exacerbated the course of the infection for > or = 47 days, compared with challenged mice that received an equivalent dose of irrelevant MAb. Oocyst excretion in feces started 4-6 days after challenge and continued at high levels for > or = 47 days. Loss of body weight was also apparent. The extent and distribution of mucosal infection were profound, involving the stomach and several segments of the small and large intestines. The acute phase, which involved infection of the gut, was during the first 25 days after challenge. The following chronic phase consistently involved, in addition, infection of the hepatobiliary tract. The acute phase is a useful model in which to test luminally active drugs, while the chronic phase may be used in the future to test drugs that are active against hepatobiliary tract infections as well.

摘要

在新生断奶的重度联合免疫缺陷(scid)小鼠受到微小隐孢子虫卵囊攻击前2小时,注射1毫克抗干扰素-γ单克隆抗体(抗IFN-γ MAb),与接受等量无关单克隆抗体的受攻击小鼠相比,显著加剧了感染病程,长达47天或更长时间。攻击后4 - 6天开始粪便中出现卵囊排泄,并持续高水平排泄47天或更长时间。体重减轻也很明显。黏膜感染的程度和分布广泛,累及胃以及小肠和大肠的多个节段。急性期涉及肠道感染,发生在攻击后的前25天。随后的慢性期除肠道感染外,还始终涉及肝胆道感染。急性期是测试腔内活性药物的有用模型,而慢性期将来可能用于测试对肝胆道感染也有活性的药物。

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