4.8 Article

Microbiota-Dependent Sequelae of Acute Infection Compromise Tissue-Specific Immunity

Journal

CELL
Volume 163, Issue 2, Pages 354-366

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2015.08.030

Keywords

-

Funding

  1. Division of Intramural Research of the National Institute of Allergy and Infectious Diseases (NIAID), NIH
  2. FAPESP [2012/14669-7]
  3. CNPq/CAPES [10986-13-8]
  4. FDA/ODS Scholarship
  5. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [12/14669-7] Funding Source: FAPESP

Ask authors/readers for more resources

Infections have been proposed as initiating factors for inflammatory disorders; however, identifying associations between defined infectious agents and the initiation of chronic disease has remained elusive. Here, we report that a single acute infection can have dramatic and long-term consequences for tissue-specific immunity. Following clearance of Yersinia pseudotuberculosis, sustained inflammation and associated lymphatic leakage in the mesenteric adipose tissue deviates migratory dendritic cells to the adipose compartment, thereby preventing their accumulation in the mesenteric lymph node. As a consequence, canonical mucosal immune functions, including tolerance and protective immunity, are persistently compromised. Post-resolution of infection, signals derived from the microbiota maintain inflammatory mesentery remodeling and consequently, transient ablation of the microbiota restores mucosal immunity. Our results indicate that persistent disruption of communication between tissues and the immune system following clearance of an acute infection represents an inflection point beyond which tissue homeostasis and immunity is compromised for the long-term.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available