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Influence of time and number of antigen encounters on memory CD8 T cell development

机译:时间和抗原接触次数对记忆CD8 T细胞发育的影响

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CD8 T cells are an important part of the adaptive immune system providing protection against intracellular bacteria, viruses, and protozoa. After infection and/or vaccination, increased numbers of antigen-specific CD8 T cells remain as a memory population that is capable of responding and providing enhanced protection during reinfection. Experimental studies indicate that while memory CD8 T cells can be maintained for great lengths of time, their properties change with time after infection and/or vaccination. However, the full scope of these changes and what effects they have on memory CD8 T cell function remain unknown. In addition, memory CD8 T cells can encounter antigen multiple times through either reinfection or prime-boost vaccine strategies designed to increase numbers of protective memory CD8 T cells. Importantly, recent studies suggest that memory CD8 T cell development following infection and/or vaccination is influenced by the number of times they have encountered cognate antigen. Since protection offered by memory CD8 T cells in response to infection depends on both the numbers and quality (functional characteristics) at the time of pathogen re-encounter, a thorough understanding of how time and antigen stimulation history impacts memory CD8 T cell properties is critical for the design of vaccines aimed at establishing populations of long-lived, protective memory CD8 T cells.
机译:CD8 T细胞是适应性免疫系统的重要组成部分,可提供针对细胞内细菌,病毒和原生动物的保护。感染和/或接种疫苗后,仍保留增加数量的抗原特异性CD8 T细胞作为记忆种群,能够在再感染期间做出反应并提供增强的保护。实验研究表明,虽然记忆CD8 T细胞可以维持很长的时间,但它们的特性在感染和/或接种疫苗后随时间而改变。但是,这些变化的全部范围以及它们对记忆CD8 T细胞功能的影响尚不清楚。此外,记忆CD8 T细胞可通过重新感染或初免-加强疫苗策略多次接触抗原,这些策略旨在增加保护性记忆CD8 T细胞的数量。重要的是,最近的研究表明,感染和/或接种疫苗后记忆CD8 T细胞的发育受它们遇到同源抗原的次数影响。由于记忆CD8 T细胞针对感染提供的保护取决于病原体再次接触时的数量和质量(功能特性),因此全面了解时间和抗原刺激史如何影响记忆CD8 T细胞特性至关重要。用于设计旨在建立长寿的保护性记忆CD8 T细胞群体的疫苗。

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