Izadjoo Mina J, Bhattacharjee Apurba K, Paranavitana Chrysanthi M, Hadfield Ted L, Hoover David L
Department of Infectious and Parasitic Diseases, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.
Infect Immun. 2004 Jul;72(7):4031-9. doi: 10.1128/IAI.72.7.4031-4039.2004.
Human brucellosis can be acquired from infected animal tissues by ingestion, inhalation, or contamination of conjunctiva or traumatized skin by infected animal products. In addition, Brucella is recognized as a biowarfare threat agent. Although a vaccine to protect humans from natural or deliberate infection could be useful, vaccines presently used in animals are unsuitable for human use. We tested orally administered live, attenuated, purine auxotrophic B. melitensis WR201 bacteria for their ability to elicit cellular and humoral immune responses and to protect mice against intranasal challenge with B. melitensis 16M bacteria. Immunized mice made serum antibody to lipopolysaccharide and non-O-polysaccharide antigens. Splenocytes from immunized animals released interleukin-2 and gamma interferon when grown in cultures with Brucella antigens. Immunization led to protection from disseminated infection and enhanced clearance of the challenge inoculum from the lungs. Optimal protection required administration of live bacteria, was related to immunizing dose, and was enhanced by booster immunization. These results establish the usefulness of oral vaccination against respiratory challenge with virulent Brucella and suggest that WR201 should be further investigated as a vaccine to prevent human brucellosis.
人类布鲁氏菌病可通过摄入、吸入感染动物组织,或感染动物产品污染结膜或创伤皮肤而获得。此外,布鲁氏菌被认为是一种生物战威胁剂。虽然一种能保护人类免受自然或蓄意感染的疫苗可能会有用,但目前用于动物的疫苗不适用于人类。我们测试了口服减毒活的嘌呤营养缺陷型羊种布鲁氏菌WR201细菌引发细胞免疫和体液免疫反应以及保护小鼠抵抗羊种布鲁氏菌16M细菌鼻内攻击的能力。免疫小鼠产生了针对脂多糖和非O-多糖抗原的血清抗体。免疫动物的脾细胞在与布鲁氏菌抗原一起培养时释放白细胞介素-2和γ干扰素。免疫可预防播散性感染,并增强从肺部清除攻击接种物的能力。最佳保护需要给予活细菌,与免疫剂量有关,并通过加强免疫得到增强。这些结果证实了口服疫苗预防强毒布鲁氏菌呼吸道攻击的有效性,并表明WR201作为预防人类布鲁氏菌病的疫苗应进一步研究。