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Uninfected Mosquito Bites Confer Protection against Infection with Malaria Parasites

机译:未感染的蚊子叮咬可预防疟疾寄生虫感染

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Despite decades of research and multiple initiatives, malaria continues to be one of the world's most debilitating infectious diseases. New insights for malaria control and vaccine development will be essential to thwart the staggering worldwide impact of this disease (A. Bjorkman and A. Bhattarai, Acta Trop. 94:163-169, 2005); ultimately successful vaccine strategies will undoubtedly be multifactorial, incorporating multiple antigens and targeting diverse aspects of the malaria parasites’ biology (M. F. Good et al., Immunol. Rev. 201:254-267, 2004). Using a murine model of malaria infection, we show here that exposure to bites from uninfected mosquitoes prior to Plasmodium yoelii infection influences the local and systemic immune responses and limits parasite development within the host. In hosts preexposed to bites from uninfected mosquitoes, reduced parasite burdens in the livers were detected early, and during the blood-stage of the life cycle, these burdens remained lower than those in hosts that received mosquito bites only at the time of infection. Repeated exposure to bites from uninfected mosquitoes skewed the immune response towards a T-helper 1 (Th1) phenotype as indicated by increased levels of interleukin-12, gamma interferon, and inducible nitric oxide synthase. These data suggest that the addition of mosquito salivary components to antimalaria vaccines may be a viable strategy for creating a Th1-biased environment known to be effective against malaria infection. Furthermore, this strategy may be important for the development of vaccines to combat other mosquito-transmitted pathogens.
机译:尽管进行了数十年的研究并采取了多种行动,但疟疾仍然是世界上最令人衰弱的传染病之一。对疟疾控制和疫苗开发的新见解对于阻止这种疾病在世界范围内的巨大影响至关重要(A. Bjorkman和A. Bhattarai,Acta Trop。94:163-169,2005);最终,成功的疫苗策略无疑将是多因素的,包括多种抗原并针对疟疾寄生虫生物学的各个方面(M. F. Good et al。,Immunol。Rev. 201:254-267,2004)。使用疟疾感染的鼠模型,我们在这里表明,在约氏疟原虫感染之前,暴露于未感染蚊子的叮咬会影响局部和全身免疫反应,并限制宿主体内的寄生虫发展。在未受到蚊子叮咬的宿主中,早期发现肝脏中的寄生虫负担降低,并且在生命周期的血液阶段,这些负担仍然低于仅在感染时受到蚊子叮咬的宿主。反复接触未感染蚊子的叮咬会使免疫应答偏向T辅助1(Th1)表型,如白介素12,γ干扰素和可诱导型一氧化氮合酶水平升高所表明。这些数据表明,在抗疟疾疫苗中添加蚊子唾液成分可能是建立Th1偏爱环境的可行策略,已知这种环境可有效对抗疟疾感染。此外,该策略对于开发抗击其他蚊子传播的病原体的疫苗可能很重要。

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