Biomedical Center, Institute for Cardiovascular Physiology and Pathophysiology, Ludwig-Maximilians-University Munich, Munich, Germany.
Walter-Brendel-Centre of Experimental Medicine, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
Front Immunol. 2019 Jan 10;9:3123. doi: 10.3389/fimmu.2018.03123. eCollection 2018.
Increased susceptibility to infectious diseases is a hallmark of the neonatal period of life that is generally attributed to a relative immaturity of the immune system. Dendritic cells (DCs) are innate immune sentinels with vital roles in the initiation and orchestration of immune responses, thus, constituting a promising target for promoting neonatal immunity. However, as is the case for other immune cells, neonatal DCs have been suggested to be functionally immature compared to their adult counterparts. Here we review some of the unique aspects of neonatal DCs that shape immune responses in early life and speculate whether the functional properties of neonatal DCs could be exploited or manipulated to promote more effective vaccination in early life.
新生儿期易患传染病是其生命阶段的一个显著特征,这通常归因于免疫系统的相对不成熟。树突状细胞(DCs)是先天免疫的哨兵,在启动和协调免疫反应中起着至关重要的作用,因此,它们是促进新生儿免疫的有希望的靶点。然而,与其他免疫细胞一样,人们认为新生儿 DC 与成人相比功能不成熟。在这里,我们回顾了塑造生命早期免疫反应的新生儿 DC 的一些独特方面,并推测新生儿 DC 的功能特性是否可以被利用或操纵,以促进生命早期更有效的疫苗接种。