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在杜克雷嗜血杆菌感染与疾病的动物模型中,使用菌毛制剂加强疫苗接种进行诱导免疫。

Inducible immunity with a pilus preparation booster vaccination in an animal model of Haemophilus ducreyi infection and disease.

作者信息

Desjardins M, Filion L G, Robertson S, Cameron D W

机构信息

Department of Medicine, University of Ottawa, Ottawa General Hospital, Ontario, Canada.

出版信息

Infect Immun. 1995 May;63(5):2012-20. doi: 10.1128/iai.63.5.2012-2020.1995.

Abstract

Using the temperature-dependent rabbit model of Haemophilus ducreyi infection as a quantitative virulence assay, we tested the abilities of two bacterial antigen preparations to induce protection against subsequent infection and disease. Lipooligosaccharide (LOS) and a pilus preparation were purified from H. ducreyi 35000 and were used in a booster immunization procedure. The serologic response to each immunogen was monitored by enzyme immunoassay. H. ducreyi virulence was assayed by intraepithelial inoculation and subsequent measurement of disease for homologous strain 35000 or clinical isolate RO-34. LOS and the pilus preparation induced humoral responses. The kinetics of the LOS antibody response suggest a type 1 T-independent response, whereas the pilus preparation induced an anamnestic response. An inoculum of 10(5) CFU of H. ducreyi 35000 or RO-34 consistently produced ulcerative chancroidal lesions in naive rabbit controls. Immunization with LOS did not modify the virulence of H. ducreyi 35000. Immunization with the strain 35000 pilus preparation significantly reduced the severity of disease and the duration of infection and disease compared with controls, with either homologous or heterologous strain infection. The histology of lesions from pilus preparation-vaccinated rabbits compared with that of lesions from controls revealed accelerated lymphoid cell recruitment, more prominent plasma cell infiltrate, and reduction in subsequent histiocytic infiltration. We conclude that both LOS and the pilus preparation are immunogenic and that the latter induces homologous and heterologous strain protection in this animal model of infection and disease.

摘要

利用温度依赖性的杜克雷嗜血杆菌感染兔模型作为定量毒力测定方法,我们测试了两种细菌抗原制剂诱导针对后续感染和疾病的保护能力。从杜克雷嗜血杆菌35000株中纯化出脂寡糖(LOS)和菌毛制剂,并用于加强免疫程序。通过酶免疫测定法监测对每种免疫原的血清学反应。通过上皮内接种并随后测量同源菌株35000或临床分离株RO - 34的疾病情况来测定杜克雷嗜血杆菌的毒力。LOS和菌毛制剂诱导了体液反应。LOS抗体反应的动力学表明是1型非T细胞依赖性反应,而菌毛制剂诱导了回忆反应。10⁵CFU的杜克雷嗜血杆菌35000或RO - 34接种物在未免疫的兔对照中始终产生溃疡性软下疳病变。用LOS免疫并未改变杜克雷嗜血杆菌35000的毒力。与对照相比,用35000株菌毛制剂免疫显著降低了疾病的严重程度以及感染和疾病的持续时间,无论是同源菌株还是异源菌株感染。与对照兔病变的组织学相比,接种菌毛制剂的兔病变组织学显示淋巴细胞募集加速、浆细胞浸润更明显,以及随后组织细胞浸润减少。我们得出结论,LOS和菌毛制剂都具有免疫原性,并且后者在这种感染和疾病动物模型中诱导了同源和异源菌株保护。

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