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Antigenic variation of TprK V regions abrogates specific antibody binding in syphilis.梅毒中TprK可变区的抗原变异可消除特异性抗体结合。
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A monoclonal antibody that conveys in vitro killing and partial protection in experimental syphilis binds a phosphorylcholine surface epitope of Treponema pallidum.一种在实验性梅毒中具有体外杀伤作用和部分保护作用的单克隆抗体可结合梅毒螺旋体的磷酸胆碱表面表位。
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梅毒螺旋体候选外膜蛋白的细胞表面暴露及疫苗原性潜力评估

Assessment of cell-surface exposure and vaccinogenic potentials of Treponema pallidum candidate outer membrane proteins.

作者信息

Tomson Farol L, Conley Patrick G, Norgard Michael V, Hagman Kayla E

机构信息

Department of Microbiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390, USA.

出版信息

Microbes Infect. 2007 Sep;9(11):1267-75. doi: 10.1016/j.micinf.2007.05.018. Epub 2007 Jun 3.

DOI:10.1016/j.micinf.2007.05.018
PMID:17890130
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2112743/
Abstract

Syphilis, a sexually transmitted infection caused by the spirochetal bacterium Treponema pallidum, remains a global public health problem. T. pallidum is believed to be an extracellular pathogen and, as such, the identification of T. pallidum outer membrane proteins that could serve as targets for opsonic or bactericidal antibodies has remained a high research priority for vaccine development. However, the identification of T. pallidum outer membrane proteins has remained highly elusive. Recent studies and bioinformatics have implicated four treponemal proteins as potential outer membrane proteins (TP0155, TP0326, TP0483 and TP0956). Indirect immunofluorescence assays performed on treponemes encapsulated within agarose gel microdroplets failed to provide evidence that any of these four molecules were surface-exposed in T. pallidum. Second, recombinant fusion proteins corresponding to all four candidate outer membrane proteins were used separately, or in combination, to vaccinate New Zealand White rabbits. Despite achieving high titers (>1:50,000) of serum antibodies, none of the rabbits displayed chancre immunity after intradermal challenge with viable T. pallidum.

摘要

梅毒是一种由螺旋体细菌梅毒螺旋体引起的性传播感染,仍然是一个全球公共卫生问题。梅毒螺旋体被认为是一种细胞外病原体,因此,鉴定可作为调理或杀菌抗体靶点的梅毒螺旋体外膜蛋白一直是疫苗开发的高度优先研究事项。然而,梅毒螺旋体外膜蛋白的鉴定一直非常困难。最近的研究和生物信息学表明有四种密螺旋体蛋白可能是外膜蛋白(TP0155、TP0326、TP0483和TP0956)。对包裹在琼脂糖凝胶微滴中的密螺旋体进行的间接免疫荧光试验未能提供证据证明这四种分子中的任何一种在梅毒螺旋体中是表面暴露的。其次,分别或联合使用与所有四种候选外膜蛋白对应的重组融合蛋白对新西兰白兔进行免疫接种。尽管血清抗体效价很高(>1:50,000),但在用活的梅毒螺旋体进行皮内攻击后,没有一只兔子表现出溃疡免疫力。