| Literature DB >> 27423204 |
Melissa J Conroy1, Karen C Galvin1, Suzanne L Doyle1,2, Maria E Kavanagh1, Ann-Marie Mongan1, Aoife Cannon1, Gillian Y Moore1, John V Reynolds1,3, Joanne Lysaght4.
Abstract
In the midst of a worsening obesity epidemic, the incidence of obesity-associated morbidities, including cancer, diabetes, cardiac and liver disease is increasing. Insights into mechanisms underlying pathological obesity-associated inflammation are lacking. Both the omentum, the principal component of visceral fat, and liver of obese individuals are sites of excessive inflammation, but to date the T cell profiles of both compartments have not been assessed or compared in a patient cohort with obesity-associated disease. We have previously identified that omentum is enriched with inflammatory cytokines, chemokines and T cells. Here, we compared the inflammatory profile of T cells in the omentum and liver of patients with the obesity-associated malignancy oesophageal adenocarcinoma (OAC). Furthermore, we assessed the secreted cytokine profile in OAC patient serum, omentum and liver to assess systemic and local inflammation. We observed parallel T cell cytokine profiles and phenotypes in the omentum and liver of OAC patients, in particular CD69(+) and inflammatory effector memory T cells. This study reflects similar processes of inflammation and T cell activation in the omentum and liver, and may suggest common targets to modulate pathological inflammation at these sites.Entities:
Keywords: T cells; cancer; inflammation; liver; obesity; omentum
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Year: 2016 PMID: 27423204 DOI: 10.1007/s10753-016-0407-2
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092