Journal
FRONTIERS IN IMMUNOLOGY
Volume 9, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2018.03123
Keywords
dendritic cell (DC); DC subsets; early life immunity; vaccination; immune system development; T cell activation; innate immunity; DC targeting
Categories
Funding
- ERC Starting Grant [ERC-2016-STG-715182]
- German Research Foundation: Emmy Noether Grant [Schr 1444/1-1, SFB914, SFB1335]
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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.
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