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类鼻疽小鼠模型中保护性免疫的发展受伯克霍尔德菌假鼻疽抗原来源的影响。

Development of protective immunity in a murine model of melioidosis is influenced by the source of Burkholderia pseudomallei antigens.

作者信息

Barnes Jodie L, Ketheesan Natkunam

机构信息

Department of Microbiology and Immunology, School of Veterinary and Biomedical Sciences, James Cook University, Townsville, Queensland, Australia.

出版信息

Immunol Cell Biol. 2007 Oct;85(7):551-7. doi: 10.1038/sj.icb.7100084. Epub 2007 Jun 12.

Abstract

Melioidosis is a potentially fatal disease caused by the bacterium, Burkholderia pseudomallei. The current study was carried out to determine the mechanisms involved in the development of protective immunity in a murine model of melioidosis. Following intravenous infection with B. pseudomallei, both C57BL/6 and BALB/c mice demonstrated delayed-type hypersensitivity responses and lymphocyte proliferation towards B. pseudomallei antigens, indicating the generation of B. pseudomallei-specific lymphocytes. Adoptive transfer of these lymphocytes to naïve C57BL/6 mice was demonstrated by a delayed-type hypersensitivity response. Mice were not protected from a subsequent lethal challenge with a highly virulent strain of B. pseudomallei, suggesting that a single intravenous dose of the bacterium is insufficient to induce a protective adaptive immune response. Attempts to induce resistance in susceptible BALB/c mice used repetitive low-dose exposure to live B. pseudomallei. Immune responses and resistance following subcutaneous immunization with live B. pseudomallei were compared with exposure to heat-killed, culture filtrate and sonicated B. pseudomallei antigens. Compared to heat-killed B. pseudomallei, significant protection was generated in BALB/c mice following immunization with live bacteria. Our studies also demonstrate that the type of immune response generated in vivo is influenced by the antigenic preparation of B. pseudomallei used for immunization.

摘要

类鼻疽是由类鼻疽伯克霍尔德菌引起的一种潜在致命疾病。开展本研究以确定类鼻疽小鼠模型中保护性免疫发展所涉及的机制。用类鼻疽伯克霍尔德菌静脉感染后,C57BL/6和BALB/c小鼠均表现出对类鼻疽伯克霍尔德菌抗原的迟发型超敏反应和淋巴细胞增殖,表明产生了类鼻疽伯克霍尔德菌特异性淋巴细胞。通过迟发型超敏反应证明了将这些淋巴细胞过继转移至未接触过抗原的C57BL/6小鼠。小鼠未受到随后用高毒力类鼻疽伯克霍尔德菌菌株进行的致死性攻击的保护,这表明单次静脉注射该细菌不足以诱导保护性适应性免疫反应。尝试通过对易感BALB/c小鼠重复低剂量暴露于活的类鼻疽伯克霍尔德菌来诱导抗性。将用活的类鼻疽伯克霍尔德菌皮下免疫后的免疫反应和抗性与暴露于热灭活、培养滤液和超声处理的类鼻疽伯克霍尔德菌抗原后的情况进行比较。与热灭活的类鼻疽伯克霍尔德菌相比,用活细菌免疫后,BALB/c小鼠产生了显著的保护作用。我们的研究还表明,体内产生的免疫反应类型受用于免疫的类鼻疽伯克霍尔德菌抗原制剂的影响。

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