Weiner D J, Soulsby E J
J Parasitol. 1976 Dec;62(6):886-93.
In each of 4 experiments, 58 multimammate rats (Mastomys natalensis) were subdivided into 5 groups. Thirty-four rats were infected with Litomosoides carinii and infections were allowed to become patent. Ten days after patency adult worms were surgically transferred from donor rats to each of 1 group of infected rats and 1 group of naive rats. Groups of infected and naive rats served as controls. Transfers were made either intrapleurally or intraperitoneally. Samples of blood and tissues were taken from each of 2 animals necropsied from each group at intervals to 31 days. At necropsy, the transferred worms and the original population (if any) were examined and samples were fixed. Infected rats accepted new worms with a minimum of reaction while naive rats rejected worms beginning at day 10 (intrapleural) of 17 (intraperitoneal). Rejections were complete leaving a white fibrous mass by day 24 or 31, respectively. Hemagglutination antibody titers fell into 2 groups: infected and naive. IHA titers of naive recipient rats increased into the infected range by day 3 (intrapleural) or day 10 (intraperitoneal). Microfilaria counts presented a more varied pattern but a similar lag in the intraperitoneal recipient group was observed. It was concluded that a preparation period is necessary for successful residence of adult worms, and that this preparation is not restricted to the pleural cavity.
在4个实验中的每一个实验里,58只多乳鼠(南非多乳鼠)被分成5组。34只大鼠感染了卡里尼丝虫,并让感染发展为显性感染。显性感染10天后,将成年虫体通过手术从供体大鼠转移到1组感染大鼠和1组未感染大鼠中的每只大鼠体内。感染组和未感染组大鼠作为对照。转移通过胸膜内或腹腔内进行。每隔一段时间直至31天,从每组剖检的2只动物身上采集血液和组织样本。在剖检时,检查转移的虫体和原来的虫群(如果有的话),并固定样本。感染大鼠对新虫体的反应极小,而未感染大鼠从第10天(胸膜内)或第17天(腹腔内)开始排斥虫体。排斥反应在第24天或31天分别完成,留下白色纤维团块。血凝抗体滴度分为两组:感染组和未感染组。未感染受体大鼠的间接血凝试验滴度在第3天(胸膜内)或第10天(腹腔内)升至感染范围内。微丝蚴计数呈现出更多样化的模式,但在腹腔内受体组中观察到了类似的滞后现象。得出的结论是,成年虫体成功驻留需要一个准备期,并且这种准备不限于胸膜腔。