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The contact pathway and sepsis

The contact pathway factors XI (FXI) and XII (FXII) have been demonstrated to be largely dispensable for hemostasis, as their absence results in a mild to absent bleeding diathesis. A growing body of literature, however, suggests that the contact pathway contributes to the pathologic host response t...

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Autores principales: Raghunathan, Vikram, Zilberman‐Rudenko, Jevgenia, Olson, Sven R., Lupu, Florea, McCarty, Owen J. T., Shatzel, Joseph J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611366/
https://www.ncbi.nlm.nih.gov/pubmed/31294319
http://dx.doi.org/10.1002/rth2.12217
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author Raghunathan, Vikram
Zilberman‐Rudenko, Jevgenia
Olson, Sven R.
Lupu, Florea
McCarty, Owen J. T.
Shatzel, Joseph J.
author_facet Raghunathan, Vikram
Zilberman‐Rudenko, Jevgenia
Olson, Sven R.
Lupu, Florea
McCarty, Owen J. T.
Shatzel, Joseph J.
author_sort Raghunathan, Vikram
collection PubMed
description The contact pathway factors XI (FXI) and XII (FXII) have been demonstrated to be largely dispensable for hemostasis, as their absence results in a mild to absent bleeding diathesis. A growing body of literature, however, suggests that the contact pathway contributes to the pathologic host response to certain infectious organisms that produces the often‐fatal syndrome known as sepsis. The contact pathway factors serve as a central node connecting inflammation to coagulation, and may offer a potentially safe therapeutic target to mitigate the morbidity and mortality associated with sepsis. Herein, we summarize published in vivo and in vitro data that have explored the roles of the contact pathway in sepsis, and discuss potential clinical applications of novel FXI‐ and FXII‐inhibiting drugs currently under investigation.
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spelling pubmed-66113662019-07-10 The contact pathway and sepsis Raghunathan, Vikram Zilberman‐Rudenko, Jevgenia Olson, Sven R. Lupu, Florea McCarty, Owen J. T. Shatzel, Joseph J. Res Pract Thromb Haemost Review Articles The contact pathway factors XI (FXI) and XII (FXII) have been demonstrated to be largely dispensable for hemostasis, as their absence results in a mild to absent bleeding diathesis. A growing body of literature, however, suggests that the contact pathway contributes to the pathologic host response to certain infectious organisms that produces the often‐fatal syndrome known as sepsis. The contact pathway factors serve as a central node connecting inflammation to coagulation, and may offer a potentially safe therapeutic target to mitigate the morbidity and mortality associated with sepsis. Herein, we summarize published in vivo and in vitro data that have explored the roles of the contact pathway in sepsis, and discuss potential clinical applications of novel FXI‐ and FXII‐inhibiting drugs currently under investigation. John Wiley and Sons Inc. 2019-05-23 /pmc/articles/PMC6611366/ /pubmed/31294319 http://dx.doi.org/10.1002/rth2.12217 Text en © 2019 The Authors Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc. on behalf of International Society on Thrombosis and Haemostasis (ISTH) This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Raghunathan, Vikram
Zilberman‐Rudenko, Jevgenia
Olson, Sven R.
Lupu, Florea
McCarty, Owen J. T.
Shatzel, Joseph J.
The contact pathway and sepsis
title The contact pathway and sepsis
title_full The contact pathway and sepsis
title_fullStr The contact pathway and sepsis
title_full_unstemmed The contact pathway and sepsis
title_short The contact pathway and sepsis
title_sort contact pathway and sepsis
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611366/
https://www.ncbi.nlm.nih.gov/pubmed/31294319
http://dx.doi.org/10.1002/rth2.12217
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