Immune checkpoint blockade targets macrophage PD-1 to exacerbate metabolic dysfunction

Immune checkpoint blockade targets macrophage PD-1 to exacerbate metabolic dysfunction

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DOI 10.1097/IN9.0000000000000079
刊名
IJ
年,卷(期) 2026, 8(2)
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作者单位

Center for Molecular Medicine (CMMC), University of Cologne, Cologne, Germany

摘要
Immune checkpoint inhibitor therapies induce metabolic dysfunction. A study by Wu et al now pinpoints macrophage programmed cell death protein 1 (PD-1) as a key molecular mediator of the anti-PD-1 treatment-triggered exacerbation of systemic metabolic disorders. Macrophage PD-1 blockade disrupts the moonlighting function of PD-1 in suppressing endoplasmic reticulum stress-mediated inflammatory responses, thereby impairing adipose tissue thermogenesis, reducing energy expenditure, and ultimately leading to systemic metabolic dysfunction.
Abstract
Immune checkpoint inhibitor therapies induce metabolic dysfunction. A study by Wu et al now pinpoints macrophage programmed cell death protein 1 (PD-1) as a key molecular mediator of the anti-PD-1 treatment-triggered exacerbation of systemic metabolic disorders. Macrophage PD-1 blockade disrupts the moonlighting function of PD-1 in suppressing endoplasmic reticulum stress-mediated inflammatory responses, thereby impairing adipose tissue thermogenesis, reducing energy expenditure, and ultimately leading to systemic metabolic dysfunction.
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Song, Zikuan; Frezza, Christian. Immune checkpoint blockade targets macrophage PD-1 to exacerbate metabolic dysfunction [J]. Immunometabolism. 2026; 8; (2). - .

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