共 50 条
Ketogenic diet activates protective γδ T cell responses against influenza virus infection
被引:98
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.
引用
收藏
页数:8
相关论文