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Protein D of Haemophilus influenzae: a protective nontypeable H. influenzae antigen and a carrier for pneumococcal conjugate vaccines.

机译:流感嗜血杆菌的蛋白D:保护性不可分型流感嗜血杆菌抗原和肺炎球菌结合疫苗的载体。

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摘要

Protein D (PD) is a highly conserved 42 kDa surface lipoprotein found in all Haemophilus influenzae, including nontypeable (NT) H. influenzae. PD is involved in the pathogenesis of respiratory tract infections, in the context of which it has been shown to impair ciliary function in a human nasopharyngeal tissue culture model and to augment the capacity to cause otitis media in rats. A likely mechanism indicating that PD is a virulence factor is its glycerophosphodiesterase activity, which leads to the release of phosphorylcholine from host epithelial cells. PD has been demonstrated to be a promising vaccine candidate against experimental NT H. influenzae infection. Rats vaccinated with PD cleared NT H. influenzae better after middle ear and pulmonary bacterial challenge, and chinchillas vaccinated with PD showed significant protection against NT H. influenzae-dependent acute otitis media. In a clinical trial involving children, PD was used as an antigenically active carrier protein in an 11-valent pneumococcal conjugate investigational vaccine; significant protection was achieved against acute otitis media not only caused by pneumococci but also caused by NT H. influenzae. This may have great clinical implications, because PD is the first NT H. influenzae antigen that has induced protective responses in humans.
机译:蛋白D(PD)是一种高度保守的42 kDa表面脂蛋白,存在于所有流感嗜血杆菌中,包括非分型(NT)流感嗜血杆菌。 PD参与呼吸道感染的发病机理,在此背景下,PD已显示出其在人鼻咽组织培养模型中损害睫状功能并增强引起大鼠中耳炎的能力。表明PD是一种致病因子的可能机制是其磷酸甘油二酸酯酶活性,该活性导致磷酸胆碱从宿主上皮细胞中释放出来。已经证明PD是针对实验性NT H.流感病毒感染的有前途的候选疫苗。接种PD疫苗的大鼠在中耳和肺部细菌攻击后能更好地清除NT H.流感,接种PD的龙猫显示出对依赖NT H.流感的急性中耳炎的显着保护作用。在一项涉及儿童的临床试验中,PD被用作11价肺炎球菌结合物研究疫苗中的一种抗原活性载体蛋白。针对由肺炎球菌引起的急性中耳炎,以及由流感嗜血杆菌引起的急性中耳炎,均获得了显着的保护。这可能具有重大的临床意义,因为PD是第一种在人类中诱导保护反应的NT H.流感抗原。

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