Vector saliva controlled inflammatory response of the host may represent the Achilles heel during pathogen transmission.

Claudia Demarta-Gatsi, Salah Mécheri
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引用次数: 5

Abstract

Infection with vector-borne pathogens starts with the inoculation of these pathogens during blood feeding. In endemic regions, the population is regularly bitten by naive vectors, implicating a permanent stimulation of the immune system by the vector saliva itself (pre-immune context). Comparatively, the number of bites received by exposed individuals from non-infected vectors is much higher than the bites from infected ones. Therefore, vector saliva and the immunological response in the skin may play an important role, so far underestimated, in the establishment of anti-pathogen immunity in endemic areas. Hence, the parasite biology and the disease pathogenesis in "saliva-primed" and "saliva-unprimed" individuals must be different. This integrated view on how the pathogen evolves within the host together with vector salivary components, which are known to be endowed with a variety of pharmacological and immunological properties, must remain the focus of any investigational study dealing with vector-borne diseases. Considering this three-way partnership, the host skin (immune system), the pathogen, and the vector saliva, the approach that consists in the validation of vector saliva as a source of molecular entities with anti-disease vaccine potential has been recently a subject of active and fruitful investigation. As an example, the vaccination with maxadilan, a potent vasodilator peptide extracted from the saliva of the sand fly Lutzomyia longipalpis, was able to protect against infection with various leishmanial parasites. More interestingly, a universal mosquito saliva vaccine that may potentially protect against a range of mosquito-borne infections including malaria, dengue, Zika, chikungunya and yellow fever. In this review, we highlight the key role played by the immunobiology of vector saliva in shaping the outcome of vector-borne diseases and discuss the value of studying diseases in the light of intimate cross talk among the pathogen, the vector saliva, and the host immune mechanisms.

Abstract Image

Abstract Image

宿主唾液控制的炎症反应可能是病原体传播过程中的致命弱点。
媒介传播的病原体感染始于在吸血期间接种这些病原体。在流行地区,人群经常被原生病媒叮咬,这意味着病媒唾液本身对免疫系统产生了永久性刺激(免疫前环境)。相比之下,暴露个体被未感染媒介叮咬的数量远高于被感染媒介叮咬的数量。因此,媒介唾液和皮肤中的免疫反应可能在流行地区建立抗病原体免疫中发挥重要作用,但迄今为止被低估。因此,“唾液启动”和“唾液未启动”个体的寄生虫生物学和疾病发病机制必然是不同的。这种关于病原体如何与媒介唾液成分(已知具有多种药理学和免疫学特性)一起在宿主内进化的综合观点,必须继续成为处理媒介传播疾病的任何调查研究的重点。考虑到这种三方伙伴关系,即宿主皮肤(免疫系统)、病原体和媒介唾液,验证媒介唾液作为具有抗病疫苗潜力的分子实体来源的方法最近已成为积极和富有成果的研究主题。例如,接种从长掌沙蝇唾液中提取的强效血管扩张肽maxadilan,能够预防各种利什曼寄生虫的感染。更有趣的是,一种通用的蚊子唾液疫苗可能会预防一系列蚊媒感染,包括疟疾、登革热、寨卡病毒、基孔肯雅热和黄热病。在本文中,我们强调了媒介唾液的免疫生物学在形成媒介传播疾病的结果中所起的关键作用,并讨论了在病原体、媒介唾液和宿主免疫机制之间密切交流的基础上研究疾病的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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