Autophagy proteins stabilize pathogen-containing phagosomes for prolonged MHC II antigen processing

自噬蛋白可稳定含病原体的吞噬体,从而延长 MHC II 抗原的处理时间

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作者:Susana Romao, Nathalie Gasser, Andrea C Becker, Bruno Guhl, Milica Bajagic, Danusia Vanoaica, Urs Ziegler, Joachim Roesler, Jörn Dengjel, Janine Reichenbach, Christian Münz

Abstract

Antigen preservation for presentation is a hallmark of potent antigen-presenting cells. In this paper, we report that in human macrophages and dendritic cells, a subset of phagosomes gets coated with Atg8/LC3, a component of the molecular machinery of macroautophagy, and maintains phagocytosed antigens for prolonged presentation on major histocompatibility complex class II molecules. These Atg8/LC3-positive phagosomes are formed around the antigen with TLR2 agonists and require reactive oxygen species production by NOX2 for their generation. A deficiency in the NOX2-dependent formation of these antigen storage phagosomes could contribute to compromise antifungal immune control in chronic granulomatous disease patients.

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