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Type I Interferons as Regulators of Human Antigen Presenting Cell Functions

期刊

TOXINS
卷 6, 期 6, 页码 1696-1723

出版社

MDPI AG
DOI: 10.3390/toxins6061696

关键词

type I interferon; dendritic cell; cell differentiation/activation; antigen uptake/processing/presentation; T cell response; transcriptional profile; microRNA

资金

  1. Associazione Italiana per la Ricerca sul Cancro (AIRC)
  2. Ricerca Finalizzata Project Italian Ministry of Health

向作者/读者索取更多资源

Type I interferons (IFNs) are pleiotropic cytokines, initially described for their antiviral activity. These cytokines exhibit a long record of clinical use in patients with some types of cancer, viral infections and chronic inflammatory diseases. It is now well established that IFN action mostly relies on their ability to modulate host innate and adaptive immune responses. Work in recent years has begun to elucidate the mechanisms by which type I IFNs modify the immune response, and this is now recognized to be due to effects on multiple cell types, including monocytes, dendritic cells (DCs), NK cells, T and B lymphocytes. An ensemble of results from both animal models and in vitro studies emphasized the key role of type I IFNs in the development and function of DCs, suggesting the existence of a natural alliance between these cytokines and DCs in linking innate to adaptive immunity. The identification of IFN signatures in DCs and their dysregulation under pathological conditions will therefore be pivotal to decipher the complexity of this DC-IFN interaction and to better exploit the therapeutic potential of these cells.

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