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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Zikuan Song
Christian Frezza
Immunometabolism
University of Cologne
Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases
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Song et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69fada7f03f892aec9b1e50b — DOI: https://doi.org/10.1097/in9.0000000000000079