Ketogenic diet activates protective γδ T cell responses against influenza virus infection

被引:97
|
作者
Goldberg, Emily L. [1 ,2 ]
Molony, Ryan D. [2 ,3 ]
Kudo, Eriko [2 ]
Sidorov, Sviatoslav [1 ]
Kong, Yong [4 ]
Dixit, Vishwa Deep [1 ,2 ,5 ]
Iwasaki, Akiko [2 ,6 ,7 ]
机构
[1] Yale Sch Med, Dept Comparat Med, New Haven, CT 06519 USA
[2] Yale Sch Med, Dept Immunobiol, New Haven, CT 06519 USA
[3] Novartis Inst BioMed Res, 250 Massachusetts Ave, Cambridge, MA 02139 USA
[4] Yale Univ, WM Keck Fdn Biotechnol Resource Lab, Dept Mol Biophys & Biochem, Sch Med, New Haven, CT 06520 USA
[5] Yale Sch Med, Yale Ctr Res Aging, New Haven, CT 06519 USA
[6] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[7] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
关键词
NLRP3; INFLAMMASOME; KETONE-BODIES; GENE; MICE; MX1; METABOLISM; GENERATION; RESISTANCE; EXPRESSION; TOLERANCE;
D O I
10.1126/sciimmunol.aav2026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Influenza A virus (IAV) infection-associated morbidity and mortality are a key global health care concern, necessitating the identification of new therapies capable of reducing the severity of IAV infections. In this study, we show that the consumption of a low-carbohydrate, high-fat ketogenic diet (KD) protects mice from lethal IAV infection and disease. KD feeding resulted in an expansion of gamma delta T cells in the lung that improved barrier functions, thereby enhancing antiviral resistance. Expansion of these protective gamma delta T cells required metabolic adaptation to a ketogenic diet because neither feeding mice a high-fat, high-carbohydrate diet nor providing chemical ketone body substrate that bypasses hepatic ketogenesis protected against infection. Therefore, KD-mediated immune-metabolic integration represents a viable avenue toward preventing or alleviating influenza disease.
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页数:8
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