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  1. Article ; Online: Antiviral anticoagulation.

    Pryzdial, Edward L G / Sutherland, Michael R / Lin, Bryan H / Horwitz, Marc

    Research and practice in thrombosis and haemostasis

    2020  Volume 4, Issue 5, Page(s) 774–788

    Abstract: ... oral anticoagulant apixaban had remarkable antiviral efficacy. SARS-CoV-2 replicates in TF-bearing ...

    Abstract 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 interconnected 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.
    Keywords covid19
    Language English
    Publishing date 2020-07-06
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 2475-0379
    ISSN (online) 2475-0379
    DOI 10.1002/rth2.12406
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Antiviral anticoagulation

    Pryzdial, Edward L. G. / Sutherland, Michael R. / Lin, Bryan H. / Horwitz, Marc

    Res. Pract. Thromb. Haemost.

    Abstract: ... oral anticoagulant apixaban had remarkable antiviral efficacy. SARS-CoV-2 replicates in TF-bearing ...

    Abstract 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 interconnected 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.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #621849
    Database COVID19

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  3. Article ; Online: Antiviral anticoagulation

    Edward L. G. Pryzdial / Michael R. Sutherland / Bryan H. Lin / Marc Horwitz

    Research and Practice in Thrombosis and Haemostasis, Vol 4, Iss 5, Pp 774-

    2020  Volume 788

    Abstract: ... oral anticoagulant apixaban had remarkable antiviral efficacy. SARS‐CoV‐2 replicates in TF‐bearing ...

    Abstract Abstract 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 interconnected 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.
    Keywords coagulation ; COVID‐19 ; herpes simplex virus ; inflammation ; protease‐activated receptor ; tissue factor ; Diseases of the blood and blood-forming organs ; RC633-647.5 ; covid19
    Subject code 570
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher Wiley
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Another new application of heparin in COVID-19: more than anticoagulation and antiviral.

    Yu, Xianqiang

    Journal of investigative medicine : the official publication of the American Federation for Clinical Research

    2021  Volume 69, Issue 6, Page(s) 1258

    MeSH term(s) Anticoagulants/therapeutic use ; Antiviral Agents/therapeutic use ; COVID-19 ; Heparin ; Humans ; SARS-CoV-2
    Chemical Substances Anticoagulants ; Antiviral Agents ; Heparin (9005-49-6)
    Language English
    Publishing date 2021-06-10
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 1217870-6
    ISSN 1708-8267 ; 0009-9279 ; 1081-5589
    ISSN (online) 1708-8267
    ISSN 0009-9279 ; 1081-5589
    DOI 10.1136/jim-2021-001951
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Research Progress on Antiviral Activity of Heparin.

    Wang, Yi / Zhang, Yanqing / Wang, Ping / Jing, Tianyuan / Hu, Yanan / Chen, Xiushan

    Current medicinal chemistry

    2023  Volume 31, Issue 1, Page(s) 7–24

    Abstract: ... for several decades. Heparin is a life-saving drug and is widely used for anticoagulation in medical practice ...

    Abstract Heparin, as a glycosaminoglycan, is known for its anticoagulant and antithrombotic properties for several decades. Heparin is a life-saving drug and is widely used for anticoagulation in medical practice. In recent years, there have been extensive studies that heparin plays an important role in non-anticoagulant diseases, such as anti-inflammatory, anti-viral, anti-angiogenesis, anti-neoplastic, anti-metastatic effects, and so on. Clinical observation and in vitro experiments indicate that heparin displays a potential multitarget effect. In this brief review, we will summarize heparin and its derivative's recently studied progress for the treatment of various viral infections. The aim is to maximize the benefits of drugs through medically targeted development, to meet the unmet clinical needs of serious viral diseases.
    MeSH term(s) Humans ; Heparin/pharmacology ; Heparin/therapeutic use ; Anticoagulants/pharmacology ; Anticoagulants/therapeutic use ; Glycosaminoglycans ; Antiviral Agents/pharmacology ; Antiviral Agents/therapeutic use ; Heparitin Sulfate
    Chemical Substances Heparin (9005-49-6) ; Anticoagulants ; Glycosaminoglycans ; Antiviral Agents ; Heparitin Sulfate (9050-30-0)
    Language English
    Publishing date 2023-02-06
    Publishing country United Arab Emirates
    Document type Review ; Journal Article
    ZDB-ID 1319315-6
    ISSN 1875-533X ; 0929-8673
    ISSN (online) 1875-533X
    ISSN 0929-8673
    DOI 10.2174/0929867330666230203124032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The role of direct oral anticoagulants in the era of COVID-19: are antiviral therapy and pharmacogenetics limiting factors?

    Roguljić, Hrvoje / Arambašić, Jerko / Ninčević, Vjera / Kuna, Lucija / Šesto, Igor / Tabll, Ashraf / Smolić, Robert / Včev, Aleksandar / Primorac, Dragan / Wu, George Y / Smolić, Martina

    Croatian medical journal

    2022  Volume 63, Issue 3, Page(s) 287–294

    Abstract: ... which makes anticoagulation an integral part of treatment. However, pharmacodynamic and pharmacokinetic ... patients due to a significant interference with antiviral agents. DOACs use in COVID-19 hospitalized ...

    Abstract In patients with COVID-19, thromboinflammation is one of the main causes of morbidity and mortality, which makes anticoagulation an integral part of treatment. However, pharmacodynamic and pharmacokinetic properties of direct oral anticoagulants (DOACs) limit the use of this class of anticoagulants in COVID-19 patients due to a significant interference with antiviral agents. DOACs use in COVID-19 hospitalized patients is currently not recommended. Furthermore, patients already on oral anticoagulant drugs should be switched to heparin at hospital admission. Nevertheless, outpatients with a confirmed diagnosis of COVID-19 are recommended to continue prior DOAC therapy. More studies are required to clarify the pathogenesis of COVID-19-induced derangement of the coagulation system in order to recommend an appropriate anticoagulant treatment.
    MeSH term(s) Administration, Oral ; Anticoagulants/therapeutic use ; Antiviral Agents/therapeutic use ; COVID-19/drug therapy ; Humans ; Inflammation ; Pharmacogenetics ; Thrombosis
    Chemical Substances Anticoagulants ; Antiviral Agents
    Language English
    Publishing date 2022-06-13
    Publishing country Croatia
    Document type Journal Article
    ZDB-ID 1157623-6
    ISSN 1332-8166 ; 0353-9504
    ISSN (online) 1332-8166
    ISSN 0353-9504
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Intravenous high dose vitamin C and selected antiviral drugs in hospitalized COVID-19 patients: a descriptive cohort study.

    Fleifel, Mohamad / Mina, Jonathan / Haykal, Tony / Asmar, Rana / El Hout, Ghida / Harb, Ranime / Dimassi, Hani / Mokhbat, Jacques / Farra, Anna / Husni-Samaha, Rola

    Journal of infection in developing countries

    2022  Volume 16, Issue 10, Page(s) 1542–1554

    Abstract: ... study in Lebanon that addresses the descriptive cohort of HDVC and antiviral therapy amongst COVID-19 ... tocilizumab, and anticoagulation as recommended in the guidelines. Statistical significance was noted ...

    Abstract Introduction: There is lack of universal agreement on the management of COVID-19. Intravenous high dose vitamin C (HDVC), remdesivir (RDV), and favipiravir (FPV) have been suggested as part of the treatment regimens and only RDV is approved by the Food and Drug Administration (FDA) so far. There is no study in Lebanon that addresses the descriptive cohort of HDVC and antiviral therapy amongst COVID-19 inpatients. Our goal was to highlight such a cohort.
    Methodology: A retrospective electronic chart review of COVID-19 inpatients was done over a period of 10 months (August 2020 to April 2021). Comparative data analysis was performed between HDVC and non-HDVC (NHDVC) groups, and RDV and FPV groups.
    Results: Among HDVC patients, 70.1% (p = 0.035) and 67.2% (p = 0.008) had dyspnea and desaturation respectively. Patients on HDVC were less likely to remain in hospital for more than 20 days (p = 0.003). HDVC patients were more likely to be on oxygen therapy with 74.7% (p = 0.002). RDV patients were more likely to be on other COVID-19-related medications during hospitalization including the use of tofacitinib, baricitinib, tocilizumab, and anticoagulation as recommended in the guidelines. Statistical significance was noted for the status on discharge as 90.1% of the patients that received RDV were discharged after clinical improvement, compared to the 74.2% of the FPV patients.
    Conclusions: Further research is needed to establish local guidelines for the treatment of COVID-19. A significant role of HDVC and FPV might resurface if randomized control trials are conducted.
    MeSH term(s) Humans ; COVID-19/drug therapy ; Antiviral Agents/therapeutic use ; SARS-CoV-2 ; Retrospective Studies ; Cohort Studies ; Ascorbic Acid/therapeutic use
    Chemical Substances Antiviral Agents ; Ascorbic Acid (PQ6CK8PD0R)
    Language English
    Publishing date 2022-10-31
    Publishing country Italy
    Document type Journal Article
    ZDB-ID 2394024-4
    ISSN 1972-2680 ; 2036-6590
    ISSN (online) 1972-2680
    ISSN 2036-6590
    DOI 10.3855/jidc.16884
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Antiviral therapy of primary cytomegalovirus infection with vascular thrombosis in immunocompetent adults.

    Deconinck, L / Flateau, C / Pichenot, M / Morell-Dubois, S / Maillard, H / Hatron, P-Y / Guery, B / Faure, K

    Medecine et maladies infectieuses

    2016  Volume 46, Issue 2, Page(s) 87–92

    Abstract: ... for the management of these infections and particularly for the antiviral therapy indication.: Methods ... another risk factor for 27 patients (42%). Only 11 patients received an antiviral therapy. A positive outcome was ... observed in all patients.: Conclusion: We suggest that antiviral therapy should be considered ...

    Abstract Background: Vascular thromboembolism (VTE) complicating cytomegalovirus (CMV) primary infection is increasingly reported in immunocompetent adults. No guideline is, however, currently available for the management of these infections and particularly for the antiviral therapy indication.
    Methods: We performed a literature review of VTE complicating CMV primary infection in immunocompetent adults using PubMed.
    Results: Sixty-nine case patients of VTE complicating CMV primary infection were reported. The main sites of venous thrombosis were the splanchnic veins (30 patients) or those of the lower limbs (18 patients). One-third of patients presented with pulmonary embolism (25 patients). Forty-nine patients (76%) had at least one VTE risk factor, inherited or acquired thrombophilia for 37 patients (58%), and another risk factor for 27 patients (42%). Only 11 patients received an antiviral therapy. A positive outcome was observed in all patients.
    Conclusion: We suggest that antiviral therapy should be considered for patients presenting with severe VTE, VTE with a negative outcome despite anticoagulation, severe organ involvement, or for patients managed in the intensive care unit.
    MeSH term(s) Antiviral Agents/therapeutic use ; Cytomegalovirus Infections/complications ; Cytomegalovirus Infections/drug therapy ; Humans ; Immunocompetence ; Thrombosis/virology
    Chemical Substances Antiviral Agents
    Language English
    Publishing date 2016-03
    Publishing country France
    Document type Journal Article ; Review
    ZDB-ID 423536-8
    ISSN 1769-6690 ; 0399-077X ; 1166-8237
    ISSN (online) 1769-6690
    ISSN 0399-077X ; 1166-8237
    DOI 10.1016/j.medmal.2015.12.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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