Antiviral anticoagulation (Record no. 52840)

MARC details
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control field MX-MdCICY
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control field 20250625162417.0
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Transcribing agency CICY
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Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-18694
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Title Antiviral anticoagulation
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Volume/sequential designation Res Pract Thromb Haemost., p.1-15, 2020
520 3# - SUMMARY, ETC.
Summary, etc. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)is a novel envelope virus that causes coronavirus disease 2019 (COVID-19). Hallmarks of COVID-19 are a puzzling form of thrombophilia that has elevated D-dimer but only modest effects on other parameters of coagulopathy. This is combined with severe inflammation, often leading to acute respiratory distress and possible lethality. Coagulopathy and inflammation are nterconnected by the transmembrane receptor, tissue factor (TF), which initiates blood clotting as a cofactor for factor VIIa (FVIIa)-mediated factor Xa (FXa)generation. TF also functions from within the nascent TF/FVIIa/FXa complex to trigger profound changes via protease-activated receptors (PARs)in many cell types, including SARS-CoV-2-trophic cells. Therefore, aberrant expression of TF may be the underlying basis of COVID-19 symptoms. Evidence suggests a correlation between infection with many virus types and development of clotting-related symptoms, ranging from heart disease to bleeding, depending on the virus. Since numerous cell types express TF and can act as sites for virus replication, a model envelope virus, herpes simplex virus type 1 (HSV1), has been used to investigate the uptake of TF into the envelope. Indeed, HSV1 and other viruses harbor surface TF antigen, which retains clotting and PAR signaling function. Strikingly, envelope TF is essential for HSV1 infection in mice, and the FXa-directed oral anticoagulant apixaban had remarkable antiviral efficacy. SARS-CoV-2 replicates in TF-bearing epithelial and endothelial cells and may stimulate and integrate host cell TF, like HSV1 and other known coagulopathic viruses. Combined with this possibility, the features of COVID-19 suggest that it is a TFopathy, and the TF/FVIIa/FXa complex is a feasible therapeutic target.
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Topical term or geographic name entry element COAGULATION
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Topical term or geographic name entry element COVID-19
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element HERPES SIMPLEX VIRUS
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Topical term or geographic name entry element INFLAMMATION
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PROTEASE-ACTIVATED RECEPTOR
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element TISSUE FACTOR
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Pryzdial, Edward L. G.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Lin, Bryan H.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Horwitz, Marc
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Personal name Sutherland, Michael R.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Horwitz, Marc
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Sutherland, Michael R.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1_1Wt6VCwRS79r_yjQPYFpibNPQu_OIHg/view?usp=drivesdk">https://drive.google.com/file/d/1_1Wt6VCwRS79r_yjQPYFpibNPQu_OIHg/view?usp=drivesdk</a>
Public note Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
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Source of classification or shelving scheme Clasificación local
Koha item type Documentos solicitados
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  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-18694 25.06.2025 25.06.2025 Documentos solicitados