White Adipose Tissue Is a Reservoir for Memory T Cells and Promotes Protective Memory Responses to Infection.

TitleWhite Adipose Tissue Is a Reservoir for Memory T Cells and Promotes Protective Memory Responses to Infection.
Publication TypeJournal Article
Year of Publication2017
AuthorsHan, S-J, Zaretsky, AGlatman, Andrade-Oliveira, V, Collins, N, Dzutsev, A, Shaik, J, da Fonseca, DMorais, Harrison, OJ, Tamoutounour, S, Byrd, AL, Smelkinson, M, Bouladoux, N, Bliska, JB, Brenchley, JM, Brodsky, IE, Belkaid, Y
JournalImmunity
Volume47
Issue6
Pagination1154-1168.e6
Date Published2017 12 19
ISSN1097-4180
KeywordsAdipose Tissue, White, Animals, Bacterial Proteins, CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Gene Expression, Genes, Reporter, Immunologic Memory, Interferon-gamma, Interleukin-17, Interleukin-5, Lipid Metabolism, Luminescent Proteins, Mice, Mice, Inbred C57BL, Mice, Transgenic, Survival Analysis, Tissue Transplantation, Toxoplasma, Toxoplasmosis, Tumor Necrosis Factor-alpha, Yersinia pseudotuberculosis, Yersinia pseudotuberculosis Infections
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.

DOI10.1016/j.immuni.2017.11.009
Alternate JournalImmunity
PubMed ID29221731
PubMed Central IDPMC5773068
Grant ListR01 AI099222 / AI / NIAID NIH HHS / United States
ZIA AI001132-06 / / Intramural NIH HHS / United States
ZIA AI001132 / AI / NIAID NIH HHS / United States
R01 AI103062 / AI / NIAID NIH HHS / United States