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1.
Muscle Nerve ; 62(2): 254-258, 2020 08.
Artículo en Inglés | MEDLINE | ID: covidwho-2209145

RESUMEN

INTRODUCTION: Coronavirus disease 2019 (COVID-19) has rapidly become a global pandemic, but little is known about its potential impact on patients with myasthenia gravis (MG). METHODS: We studied the clinical course of COVID-19 in five hospitalized patients with autoimmune MG (four with acetylcholine receptor antibodies, one with muscle-specific tyrosine kinase antibodies) between April 1, 2020-April 30-2020. RESULTS: Two patients required intubation for hypoxemic respiratory failure, whereas one required significant supplemental oxygen. One patient with previously stable MG had myasthenic exacerbation. One patient treated with tocilizumab for COVID-19 was successfully extubated. Two patients were treated for MG with intravenous immunoglobulin without thromboembolic complications. DISCUSSION: Our findings suggest that the clinical course and outcomes in patients with MG and COVID-19 are highly variable. Further large studies are needed to define best practices and determinants of outcomes in this unique population.


Asunto(s)
Anticuerpos Monoclonales Humanizados/uso terapéutico , Infecciones por Coronavirus/terapia , Hipoxia/terapia , Inmunoglobulinas Intravenosas/uso terapéutico , Factores Inmunológicos/uso terapéutico , Miastenia Gravis/terapia , Neumonía Viral/terapia , Insuficiencia Respiratoria/terapia , Adulto , Anciano de 80 o más Años , Betacoronavirus , COVID-19 , Infecciones por Coronavirus/complicaciones , Infecciones por Coronavirus/tratamiento farmacológico , Progresión de la Enfermedad , Femenino , Humanos , Hipoxia/etiología , Inmunosupresores/uso terapéutico , Intubación Intratraqueal , Masculino , Persona de Mediana Edad , Miastenia Gravis/complicaciones , Miastenia Gravis/inmunología , Terapia por Inhalación de Oxígeno , Pandemias , Neumonía Viral/complicaciones , Proteínas Tirosina Quinasas Receptoras/inmunología , Receptores Colinérgicos/inmunología , Respiración Artificial , Insuficiencia Respiratoria/etiología , SARS-CoV-2 , Tratamiento Farmacológico de COVID-19
2.
Biochim Biophys Acta Mol Cell Res ; 1868(6): 118992, 2021 05.
Artículo en Inglés | MEDLINE | ID: covidwho-1103718

RESUMEN

Receptor Tyrosine Kinases are critical regulators of signal transduction that support cell survival, proliferation, and differentiation. Dysregulation of normal Receptor Tyrosine Kinase function by mutation or other activity-altering event can be oncogenic or can impact the transformed malignant cell so it becomes particularly resistant to stress challenge, have increased proliferation, become evasive to immune surveillance, and may be more prone to metastasis of the tumor to other organ sites. The TAM family of Receptor Tyrosine Kinases (TYRO3, AXL, MERTK) is emerging as important components of malignant cell survival in many cancers. The TAM kinases are important regulators of cellular homeostasis and proper cell differentiation in normal cells as receptors for their ligands GAS6 and Protein S. They also are critical to immune and inflammatory processes. In malignant cells, the TAM kinases can act as ligand independent co-receptors to mutant Receptor Tyrosine Kinases and in some cases (e.g. FLT3-ITD mutant) are required for their function. They also have a role in immune checkpoint surveillance. At the time of this review, the Covid-19 pandemic poses a global threat to world health. TAM kinases play an important role in host response to many viruses and it is suggested the TAM kinases may be important in aspects of Covid-19 biology. This review will cover the TAM kinases and their role in these processes.


Asunto(s)
Muerte Celular , Inmunidad , Proteínas Tirosina Quinasas Receptoras/inmunología , Virosis/inmunología , Animales , COVID-19/genética , COVID-19/inmunología , COVID-19/metabolismo , Humanos , Inflamación/genética , Inflamación/inmunología , Inflamación/metabolismo , Mutación , Neoplasias/genética , Neoplasias/inmunología , Neoplasias/metabolismo , Proteínas Tirosina Quinasas Receptoras/genética , Proteínas Tirosina Quinasas Receptoras/metabolismo , Virosis/genética , Virosis/metabolismo
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