自噬
生物
免疫系统
细胞生物学
先天免疫系统
免疫学
T细胞
先天性淋巴细胞
抗原呈递
癌症研究
细胞凋亡
生物化学
作者
Manuela Giansanti,Tobias Theinert,Sarah Katharina Boeing,Dorothee Haas,Paul‐Gerhardt Schlegel,Paola Vacca,Francesca Nazio,Ignazio Caruana
标识
DOI:10.1186/s12943-023-01893-w
摘要
Abstract Autophagy is an essential cellular homeostasis pathway initiated by multiple stimuli ranging from nutrient deprivation to viral infection, playing a key role in human health and disease. At present, a growing number of evidence suggests a role of autophagy as a primitive innate immune form of defense for eukaryotic cells, interacting with components of innate immune signaling pathways and regulating thymic selection, antigen presentation, cytokine production and T/NK cell homeostasis. In cancer, autophagy is intimately involved in the immunological control of tumor progression and response to therapy. However, very little is known about the role and impact of autophagy in T and NK cells, the main players in the active fight against infections and tumors. Important questions are emerging: what role does autophagy play on T/NK cells? Could its modulation lead to any advantages? Could specific targeting of autophagy on tumor cells (blocking) and T/NK cells (activation) be a new intervention strategy? In this review, we debate preclinical studies that have identified autophagy as a key regulator of immune responses by modulating the functions of different immune cells and discuss the redundancy or diversity among the subpopulations of both T and NK cells in physiologic context and in cancer.
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