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Cited by 425

The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.

Innate and Adaptive Immunity through Autophagy

Open access
Schmid, Dorothee, Münz, Christian·2007·Immunity

Abstract

The two main proteolytic machineries of eukaryotic cells, lysosomes and proteasomes, receive substrates by different routes. Polyubiquitination targets proteins for proteasomal degradation, whereas autophagy delivers intracellular material for lysosomal hydrolysis. The importance of autophagy for cell survival has long been appreciated, but more recently, its essential role in both innate and adaptive immunity has been characterized. Autophagy is now recognized to restrict viral infections and replication of intracellular bacteria and parasites. Additionally, this pathway delivers cytoplasmic antigens for MHC class II presentation to the adaptive immune system, which then in turn is able to regulate autophagy. At the same time, autophagy plays a role in the survival and the cell death of T cells. Thus, the immune system utilizes autophagic degradation of cytoplasmic material, to both restrict intracellular pathogens and regulate adaptive immunity.

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Crossref · 10.1016/j.immuni.2007.07.004

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Metadata

Authors
Schmid, D., & Münz, C.
Venue
Immunity
Publisher
Elsevier BV
Published
2007-07
Volume
27
Issue
1
Pages
11-21
ISSN
1074-7613 (ISSN-L)
OpenAlex
W2046428284
Cited by
425
References
17
FWCI
27.01
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Innate and Adaptive Immunity through Autophagy. https://app.cochat.ai/papers/10.1016/j.immuni.2007.07.004
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Schmid, D., & Münz, C. (2007). Innate and Adaptive Immunity through Autophagy. Immunity. https://doi.org/10.1016/j.immuni.2007.07.004

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.