| Literature DB >> 29221731 |
Seong-Ji Han1, Arielle Glatman Zaretsky1, Vinicius Andrade-Oliveira1, Nicholas Collins1, Amiran Dzutsev2, Jahangheer Shaik1, Denise Morais da Fonseca1, Oliver J Harrison1, Samira Tamoutounour1, Allyson L Byrd3, Margery Smelkinson4, Nicolas Bouladoux5, James B Bliska6, Jason M Brenchley7, Igor E Brodsky8, Yasmine Belkaid9.
Abstract
White adipose tissue bridges body organs and plays a fundamental role in host metabolism. To what extent adipose tissue also contributes to immune surveillance and long-term protective defense remains largely unknown. Here, we have shown that at steady state, white adipose tissue contained abundant memory lymphocyte populations. After infection, white adipose tissue accumulated large numbers of pathogen-specific memory T cells, including tissue-resident cells. Memory T cells in white adipose tissue expressed a distinct metabolic profile, and white adipose tissue from previously infected mice was sufficient to protect uninfected mice from lethal pathogen challenge. Induction of recall responses within white adipose tissue was associated with the collapse of lipid metabolism in favor of antimicrobial responses. Our results suggest that white adipose tissue represents a memory T cell reservoir that provides potent and rapid effector memory responses, positioning this compartment as a potential major contributor to immunological memory. Published by Elsevier Inc.Entities:
Keywords: T cells; adipocytes; adipose tissue; central memory T cells; effector memory T cells; infection; lipids; memory; metabolism; resident memory T cells
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Year: 2017 PMID: 29221731 PMCID: PMC5773068 DOI: 10.1016/j.immuni.2017.11.009
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745