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肺炎球菌多样性:关于新疫苗策略的考量,重点关注肺炎球菌表面蛋白A(PspA)

Pneumococcal diversity: considerations for new vaccine strategies with emphasis on pneumococcal surface protein A (PspA).

作者信息

Briles D E, Tart R C, Swiatlo E, Dillard J P, Smith P, Benton K A, Ralph B A, Brooks-Walter A, Crain M J, Hollingshead S K, McDaniel L S

机构信息

Departments of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294-2170, USA.

出版信息

Clin Microbiol Rev. 1998 Oct;11(4):645-57. doi: 10.1128/CMR.11.4.645.

Abstract

Streptococcus pneumoniae is a problematic infectious agent, whose seriousness to human health has been underscored by the recent rise in the frequency of isolation of multidrug-resistant strains. Pneumococcal pneumonia in the elderly is common and often fatal. Young children in the developing world are at significant risk for fatal pneumococcal respiratory disease, while in the developed world otitis media in children results in substantial economic costs. Immunocompromised patients are extremely susceptible to pneumococcal infection. With 90 different capsular types thus far described, the diversity of pneumococci contributes to the challenges of preventing and treating S. pneumoniae infections. The current capsular polysaccharide vaccine is not recommended for use in children younger than 2 years and is not fully effective in the elderly. Therefore, innovative vaccine strategies to protect against this agent are needed. Given the immunogenic nature of S. pneumoniae proteins, these molecules are being investigated as potential vaccine candidates. Pneumococcal surface protein A (PspA) has been evaluated for its ability to elicit protection against S. pneumoniae infection in mouse models of systemic and local disease. This review focuses on immune system responsiveness to PspA and the ability of PspA to elicit cross-protection against heterologous strains. These parameters will be critical to the design of broadly protective pneumococcal vaccines.

摘要

肺炎链球菌是一种有问题的感染源,耐多药菌株分离频率最近上升,凸显了其对人类健康的严重性。老年人的肺炎球菌肺炎很常见,且往往致命。发展中世界的幼儿面临致命性肺炎球菌呼吸道疾病的重大风险,而在发达世界,儿童中耳炎造成了巨大的经济成本。免疫功能低下的患者极易感染肺炎球菌。迄今已描述了90种不同的荚膜类型,肺炎球菌的多样性给预防和治疗肺炎链球菌感染带来了挑战。目前的荚膜多糖疫苗不推荐用于2岁以下儿童,对老年人也不完全有效。因此,需要创新的疫苗策略来预防这种病原体。鉴于肺炎链球菌蛋白质的免疫原性,这些分子正作为潜在的疫苗候选物进行研究。肺炎球菌表面蛋白A(PspA)已在全身性和局部疾病的小鼠模型中评估其引发针对肺炎链球菌感染的保护作用的能力。本综述重点关注免疫系统对PspA的反应以及PspA引发针对异源菌株的交叉保护的能力。这些参数对于设计具有广泛保护作用的肺炎球菌疫苗至关重要。

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