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The Immune Nature of Platelets Revisited

Open access
Maouia, Amal, Rebetz, Johan, Kapur, Rick, Semple, John W.·2020·Transfusion Medicine Reviews

Abstract

Platelets are the primary cellular mediators of hemostasis and this function firmly acquaints them with a variety of inflammatory processes. For example, platelets can act as circulating sentinels by expressing Toll-like receptors (TLR) that bind pathogens and this allows platelets to effectively kill them or present them to cells of the immune system. Furthermore, activated platelets secrete and express many pro- and anti-inflammatory molecules that attract and capture circulating leukocytes and direct them to inflamed tissues. In addition, platelets can directly influence adaptive immune responses via secretion of, for example, CD40 and CD40L molecules. Platelets are also the source of most of the microvesicles in the circulation and these miniscule elements further enhance the platelet’s ability to communicate with the immune system. More recently, it has been demonstrated that platelets and their parent cells, the MK, can also uptake, process and present both foreign and self-antigens to CD8+ T-cells conferring on them the ability to directly alter adaptive immune responses. This review will highlight several of the non-hemostatic attributes of platelets that clearly and rightfully place them as integral players in immune reactions.

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Metadata

Authors
Maouia, A., Rebetz, J., Kapur, R., & Semple, J. W.
Venue
Transfusion Medicine Reviews
Publisher
Elsevier BV
Published
2020-10
Volume
34
Issue
4
Pages
209-220
ISSN
0887-7963 (ISSN-L)
OpenAlex
W3087279172
Cited by
238
References
10
FWCI
13.50
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: The Immune Nature of Platelets Revisited. https://app.cochat.ai/papers/10.1016/j.tmrv.2020.09.005
The paper
Maouia, A., Rebetz, J., Kapur, R., & Semple, J. W. (2020). The Immune Nature of Platelets Revisited. Transfusion Medicine Reviews. https://doi.org/10.1016/j.tmrv.2020.09.005

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

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