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用等渗阳离子脂质体包被物(ISCOMs)口服接种鸡球虫表面子孢子蛋白的小鼠的免疫反应和保护作用

Immune responses and protective effect in mice vaccinated orally with surface sporozoite protein of Eimeria falciformis in ISCOMs.

作者信息

Kazanji M, Laurent F, Péry P

机构信息

INRA, Unité de Virologie et Immunologie Moléculaires, Jouy-en-Josas, France.

出版信息

Vaccine. 1994 Jul;12(9):798-804. doi: 10.1016/0264-410x(94)90288-7.

DOI:10.1016/0264-410x(94)90288-7
PMID:7975858
Abstract

Immunostimulating complexes (ISCOMs) were built after treatment of a purified surface protein from Eimeria falciformis sporozoites with a palmitic acid derivation, leading to a high ratio (33-64%) of P27 incorporation in these cage-like structures. P27 kept its antigenicity after incorporation in ISCOMs, which induced, after iterative intubations by the oral route to groups of mice, a systemic IgG response, a local IgA response, and a local enhanced cellular response as demonstrated by lymphoproliferation of mesenteric lymph node cells upon in vitro stimulation with antigen. This immunization (120 micrograms in six oral doses at 2-day intervals) afforded mice a partial protection (60%) against a subsequent 400 oocyst challenge. The reduction in daily oocyst excretion was corroborated by significantly different weight losses between immunized and control mice on days 9 and 10 postinfection and the subsequent death of these control mice. These observations provide the first application of ISCOMs to parasitic intestinal diseases.

摘要

免疫刺激复合物(ISCOMs)是在用棕榈酸衍生物处理来自恶性疟原虫子孢子的纯化表面蛋白后构建而成的,这使得P27以高比例(33 - 64%)掺入这些笼状结构中。P27掺入ISCOMs后仍保持其抗原性,经对小鼠组进行多次口服插管后,诱导了全身性IgG反应、局部IgA反应以及局部增强的细胞反应,这通过体外抗原刺激后肠系膜淋巴结细胞的淋巴细胞增殖得以证明。这种免疫(分六次口服剂量,每次120微克,间隔2天)使小鼠对随后400个卵囊的攻击获得了部分保护(60%)。感染后第9天和第10天,免疫小鼠和对照小鼠之间显著不同的体重减轻以及随后对照小鼠的死亡证实了每日卵囊排泄量的减少。这些观察结果首次将ISCOMs应用于寄生性肠道疾病。

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