Lauvau Grégoire, Boutet Marie, Williams Tere M, Chin Shu Shien, Chorro Laurent
Albert Einstein College of Medicine, Department of Microbiology and Immunology, New York, NY, USA.
Albert Einstein College of Medicine, Department of Microbiology and Immunology, New York, NY, USA.
Trends Immunol. 2016 Jun;37(6):375-385. doi: 10.1016/j.it.2016.04.001. Epub 2016 Apr 27.
Recent findings have revealed roles for systemic and mucosa-resident memory CD8(+) T cells in the orchestration of innate immune responses critical to host defense upon microbial infection. Here we integrate these findings into the current understanding of the molecular and cellular signals controlling memory CD8(+) T cell reactivation and the mechanisms by which these cells mediate effective protection in vivo. The picture that emerges presents memory CD8(+) T cells as early sensors of danger signals, mediating protective immunity both through licensing of cellular effectors of the innate immune system and via the canonical functions associated with memory T cells. We discuss implications for the development of T cell vaccines and therapies and highlight important areas in need of further investigation.
最近的研究结果揭示了全身和黏膜驻留记忆性CD8(+) T细胞在协调先天性免疫反应中的作用,这些反应对于宿主抵御微生物感染至关重要。在此,我们将这些研究结果整合到当前对控制记忆性CD8(+) T细胞重新激活的分子和细胞信号以及这些细胞在体内介导有效保护的机制的理解中。由此呈现出的情况是,记忆性CD8(+) T细胞是危险信号的早期传感器,通过赋予先天性免疫系统的细胞效应器许可以及通过与记忆性T细胞相关的经典功能来介导保护性免疫。我们讨论了对T细胞疫苗和疗法开发的影响,并强调了需要进一步研究的重要领域。