Using heparin molecules to manage COVID‐2019
The coronavirus disease 2019 (COVID‐19) pandemic is becoming one of the largest global public health crises in modern history. The race for an effective drug to prevent or treat the infection is the highest priority among health care providers, government officials, and the pharmaceutical industry....
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Published in | Research and practice in thrombosis and haemostasis Vol. 4; no. 4; pp. 518 - 523 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.05.2020
Elsevier Limited John Wiley and Sons Inc Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | The coronavirus disease 2019 (COVID‐19) pandemic is becoming one of the largest global public health crises in modern history. The race for an effective drug to prevent or treat the infection is the highest priority among health care providers, government officials, and the pharmaceutical industry. Recent evidence reports that the use of low‐molecular‐weight heparin reduces mortality in patients with severe coronavirus with coagulopathy. Although the full scope of the benefits from heparin for COVID‐19 patients is unfolding, encouraging clinical data suggest that heparin‐like molecules may represent a useful approach to treat or prevent severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection. The intent of this article is to offer our opinions on the mechanism(s) by which heparin may attenuate the course of SARS‐CoV‐2 infection. Furthermore, we propose a novel strategy to treat or prevent SARS‐CoV‐2 infection using “designer” heparin molecules that are fabricated using a synthetic biology approach. |
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Bibliography: | Funding information Handling Editor: Yotis Senis This work is supported in part by NIH grants (HL094463, HL144970, HL146226 and HL 142604). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ISSN: | 2475-0379 2475-0379 |
DOI: | 10.1002/rth2.12353 |