Department of Molecular Microbiology and Immunology and Johns Hopkins Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Proc Natl Acad Sci U S A. 2013 May 28;110(22):9090-5. doi: 10.1073/pnas.1303858110. Epub 2013 May 14.
CD8(+) T cells are specialized cells of the adaptive immune system capable of finding and eliminating pathogen-infected cells. To date it has not been possible to observe the destruction of any pathogen by CD8(+) T cells in vivo. Here we demonstrate a technique for imaging the killing of liver-stage malaria parasites by CD8(+) T cells bearing a transgenic T cell receptor specific for a parasite epitope. We report several features that have not been described by in vitro analysis of the process, chiefly the formation of large clusters of effector CD8(+) T cells around infected hepatocytes. The formation of clusters requires antigen-specific CD8(+) T cells and signaling by G protein-coupled receptors, although CD8(+) T cells of unrelated specificity are also recruited to clusters. By combining mathematical modeling and data analysis, we suggest that formation of clusters is mainly driven by enhanced recruitment of T cells into larger clusters. We further show various death phenotypes of the parasite, which typically follow prolonged interactions between infected hepatocytes and CD8(+) T cells. These findings stress the need for intravital imaging for dissecting the fine mechanisms of pathogen recognition and killing by CD8(+) T cells.
CD8(+) T 细胞是适应性免疫系统的专门细胞,能够发现并清除受病原体感染的细胞。迄今为止,还不可能在体内观察到 CD8(+) T 细胞对任何病原体的破坏。在这里,我们展示了一种用于观察携带针对寄生虫表位的转基因 T 细胞受体的 CD8(+) T 细胞杀伤肝期疟原虫的技术。我们报告了一些通过体外分析该过程未描述的特征,主要是在受感染的肝细胞周围形成效应 CD8(+) T 细胞的大簇。簇的形成需要抗原特异性 CD8(+) T 细胞和 G 蛋白偶联受体的信号传导,尽管非相关特异性的 CD8(+) T 细胞也被招募到簇中。通过结合数学建模和数据分析,我们提出簇的形成主要是由 T 细胞向更大的簇的增强募集驱动的。我们进一步展示了寄生虫的各种死亡表型,这些表型通常遵循受感染的肝细胞和 CD8(+) T 细胞之间的长时间相互作用。这些发现强调了需要进行活体成像以剖析 CD8(+) T 细胞识别和杀伤病原体的精细机制。