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Cited by 569

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Exosomes and tumor-mediated immune suppression

Open access
Whiteside, Theresa L.·2016·Journal of Clinical Investigation

Abstract

Tumor-derived exosomes (TEX) are harbingers of tumor-induced immune suppression: they carry immunosuppressive molecules and factors known to interfere with immune cell functions. By delivering suppressive cargos consisting of proteins similar to those in parent tumor cells to immune cells, TEX directly or indirectly influence the development, maturation, and antitumor activities of immune cells. TEX also deliver genomic DNA, mRNA, and microRNAs to immune cells, thereby reprogramming functions of responder cells to promote tumor progression. TEX carrying tumor-associated antigens can interfere with antitumor immunotherapies. TEX also have the potential to serve as noninvasive biomarkers of tumor progression. In the tumor microenvironment, TEX may be involved in operating numerous signaling pathways responsible for the downregulation of antitumor immunity.

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Crossref · 10.1172/jci81136

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9 of 9 references verified0 citation errors · 0 not checkable

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Metadata

Authors
Whiteside, T. L.
Venue
Journal of Clinical Investigation
Published
2016-02-29
Volume
126
Issue
4
Pages
1216-1223
ISSN
  • 0021-9738 (ISSN-L)
  • 1558-8238
OpenAlex
W2292821496
Cited by
569
References
9
FWCI
21.67
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Exosomes and tumor-mediated immune suppression. https://app.cochat.ai/papers/10.1172/jci81136
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Whiteside, T. L. (2016). Exosomes and tumor-mediated immune suppression. Journal of Clinical Investigation. https://doi.org/10.1172/jci81136

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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.