Integrating innate and adaptive immunity in the whole animal.

Abstract:

:The mammalian defense system can respond to a variety of threats, but this capability is not just a simple alarm system for triggering antigen-presenting cells and initiating cellular immunity. Instead, the body is an integrated system in which nearly every cell type can relay the alarm through the production of chemokines, which recruit specific inflammatory cells to the target tissues. This chemokine production is carefully regulated at several levels so that the kinetics and character of local tissue inflammation is tailored to the specific threat. First, the production of nuclear factor-kappa B-regulated chemokines can be modulated in non-bone marrow-derived cells through transcriptional repression mediated by RelB. RelB is also implicated in the differentiation of lymphoid dendritic cells, suggesting that this gene regulates the transition from acute inflammation to adaptive immunity. Second, tissue parenchymal cells, in their capacity as sentinel cells, are able to produce different patterns of chemokines in response to different alarm stimuli. Third, cells from different tissues also show distinct potentials for chemokine responses so that the non-specific damage from inflammation might be avoided in some cases. Finally, the differentiation of T-cell effectors allows for further regulation of local inflammation as their cytokines can also affect chemokine production. This integration of innate and adaptive immunity allows for both rapid responses and dynamic regulation of inflammation in vivo.

journal_name

Immunol Rev

journal_title

Immunological reviews

authors

Lo D,Feng L,Li L,Carson MJ,Crowley M,Pauza M,Nguyen A,Reilly CR

doi

10.1111/j.1600-065x.1999.tb01318.x

keywords:

subject

Has Abstract

pub_date

1999-06-01 00:00:00

pages

225-39

eissn

0105-2896

issn

1600-065X

journal_volume

169

pub_type

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