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1.
Front Immunol ; 12: 687534, 2021.
Artículo en Inglés | MEDLINE | ID: covidwho-1295639

RESUMEN

The clinical significance of antiphospholipid antibodies (aPL) in the context of infections has attracted attention since their first discovery in patients with syphilis. In fact, the recognition of aPL in patients with infections has been described in parallel to the understating of the syndrome. Since the first description of aPL-positive tests in three patients with COVID-19 diagnosed in January 2020 in Wuhan, China, a large number of studies took part in the ongoing debate on SARS-2-Cov 2 induced coagulopathy, and many following reports speculated a potential role for aPL. In order to get further insights on the effective role of detectable aPL in the pro-thrombotic status observed in COVID-19 patients, we performed an observational age-sex controlled study to compare the aPL profile of hospitalized patients with COVID with those observed in a) patients with thrombotic APS and b) patients with cultural/serologically-proved infections. Our data showed positive aPL testing in about half of the patients (53%) with COVID-19 and patients with other viral/bacterial infections (49%). However, aPL profile was different when comparing patients with overt APS and patients with aPL detected in the contest of infections. Caution is therefore required in the interpretation and generalization of the role of aPL s in the management of patients with COVID-19. Before introducing aPL testing as a part of the routine testing in patients with COVID-19, larger well-designed clinical studies are required. While the pro-thrombotic status in patients with COVID-19 is now unquestionable, different mechanisms other than aPL should be further investigated.


Asunto(s)
Anticuerpos Antifosfolípidos/sangre , Síndrome Antifosfolípido/patología , Infecciones Bacterianas/patología , COVID-19/patología , Coagulación Intravascular Diseminada/patología , Virosis/patología , Anciano , Anticuerpos Antifosfolípidos/inmunología , Síndrome Antifosfolípido/complicaciones , Síndrome Antifosfolípido/inmunología , Infecciones Bacterianas/complicaciones , COVID-19/complicaciones , COVID-19/inmunología , Coagulación Intravascular Diseminada/virología , Femenino , Humanos , Masculino , SARS-CoV-2/inmunología , Virosis/complicaciones
2.
Prostaglandins Other Lipid Mediat ; 154: 106540, 2021 06.
Artículo en Inglés | MEDLINE | ID: covidwho-1096205

RESUMEN

Coronavirus Disease 2019 (COVID-19) is upsetting the world and innovative therapeutic solutions are needed in an attempt to counter this new pandemic. Great hope lies in vaccines, but drugs to cure the infected patient are just as necessary. In the most severe forms of the disease, a cytokine storm with neuroinflammation occurs, putting the patient's life at serious risk, with sometimes long-lasting sequelae. Palmitoylethanolamide (PEA) is known to possess anti-inflammatory and neuroprotective properties, which make it an ideal candidate to be assumed in the earliest stage of the disease. Here, we provide a mini-review on the topic, pointing out phospholipids consumption in COVID-19, the possible development of an antiphospholipid syndrome secondary to SARS-CoV-2 infection, and reporting our preliminary single-case experience concerning to a 45-year-old COVID-19 female patient recently treated with success by micronized / ultramicronized PEA.


Asunto(s)
Amidas/administración & dosificación , Antiinflamatorios/administración & dosificación , Síndrome Antifosfolípido/tratamiento farmacológico , Tratamiento Farmacológico de COVID-19 , Etanolaminas/administración & dosificación , Fármacos Neuroprotectores/administración & dosificación , Ácidos Palmíticos/administración & dosificación , SARS-CoV-2/metabolismo , Síndrome Antifosfolípido/etiología , Síndrome Antifosfolípido/metabolismo , Síndrome Antifosfolípido/patología , COVID-19/complicaciones , COVID-19/metabolismo , COVID-19/patología , Femenino , Humanos , Persona de Mediana Edad
3.
Int J Mol Med ; 46(3): 903-912, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: covidwho-750592

RESUMEN

The severe acute respiratory syndrome coronavirus 2 (SARS­CoV­2) is a novel ß coronavirus that is the etiological agent of the pandemic coronavirus disease 2019 (COVID­19) that at the time of writing (June 16, 2020) has infected almost 6 million people with some 450,000 deaths. These numbers are still rising daily. Most (some 80%) cases of COVID­19 infection are asymptomatic, a substantial number of cases (15%) require hospitalization and an additional fraction of patients (5%) need recovery in intensive care units. Mortality for COVID­19 infection appears to occur globally between 0.1 and 0.5% of infected patients although the frequency of lethality is significantly augmented in the elderly and in patients with other comorbidities. The development of acute respiratory distress syndrome and episodes of thromboembolism that may lead to disseminated intravascular coagulation (DIC) represent the primary causes of lethality during COVID­19 infection. Increasing evidence suggests that thrombotic diathesis is due to multiple derangements of the coagulation system including marked elevation of D­dimer that correlate negatively with survival. We propose here that the thromboembolic events and eventually the development of DIC provoked by SARS­CoV­2 infection may represent a secondary anti­phospholipid antibody syndrome (APS). We will apply both Baconian inductivism and Cartesian deductivism to prove that secondary APS is likely responsible for coagulopathy during the course of COVID­19 infection. Diagnostic and therapeutic implications of this are also discussed.


Asunto(s)
Síndrome Antifosfolípido/patología , Infecciones por Coronavirus/patología , Coagulación Intravascular Diseminada/patología , Neumonía Viral/patología , Tromboembolia/patología , Trombosis/patología , Síndrome Antifosfolípido/inmunología , Antivirales/uso terapéutico , Betacoronavirus , Coagulación Sanguínea/fisiología , COVID-19 , Infecciones por Coronavirus/tratamiento farmacológico , Infecciones por Coronavirus/inmunología , Coagulación Intravascular Diseminada/inmunología , Productos de Degradación de Fibrina-Fibrinógeno/metabolismo , Humanos , Pandemias , Fosfolípidos/inmunología , Neumonía Viral/tratamiento farmacológico , Neumonía Viral/inmunología , SARS-CoV-2 , Tromboembolia/inmunología
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