Istituto Nazionale Genetica Molecolare "Romeo ed Enrica Invernizzi," Milan , Italy.
Front Immunol. 2014 Feb 10;5:43. doi: 10.3389/fimmu.2014.00043. eCollection 2014.
Induction of the adaptive immune system is evaluated mostly by assessment of serum antibody titers and T lymphocyte responses in peripheral blood, although T and B cell activation occurs in lymphoid tissues. In recent years, the release of microRNAs (miRNAs) in the extra-cellular environment has been exploited to assess cell functions at distance via measurement of serum miRNAs. Activated lymphocytes release a large amount of nano-sized vesicles (exosomes), containing miRNA, however there are insufficient data to determine whether this phenomenon is reflected in modulation of serum miRNAs. Interestingly, miRNA signatures of CD4(+) T cell-derived exosomes are substantially different from intracellular miRNA signatures of the same cells. We have recently identified serum circulating miR-150 as a sensor of general lymphocyte activation and we strongly believe that miRNAs differentially released by specific CD4(+) effector T cell subsets (Th1, Th2, Th17, and Treg) may serve as serum biomarkers of their elicitation in lymphoid tissues but also in damaged tissues, potentially providing clinically relevant information about the nature of immune responses in health and disease.
适应性免疫系统的诱导主要通过评估血清抗体滴度和外周血 T 淋巴细胞反应来评估,尽管 T 细胞和 B 细胞的激活发生在淋巴组织中。近年来,细胞外环境中 microRNAs(miRNAs)的释放已被用于通过测量血清 miRNAs 来评估远距离的细胞功能。活化的淋巴细胞会释放大量纳米大小的囊泡(外泌体),其中包含 miRNA,但目前尚无足够的数据来确定这种现象是否反映在血清 miRNAs 的调节中。有趣的是,CD4(+)T 细胞来源的外泌体中的 miRNA 特征与同一细胞内的 miRNA 特征有很大的不同。我们最近发现血清循环 miR-150 是一般淋巴细胞活化的传感器,我们坚信,特定 CD4(+)效应 T 细胞亚群(Th1、Th2、Th17 和 Treg)释放的 miRNA 可能作为其在淋巴组织中诱导的血清生物标志物,也可能作为受损组织中诱导的血清生物标志物,可能为健康和疾病中免疫反应的性质提供临床相关信息。