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1.
Viruses ; 13(11)2021 11 08.
Artículo en Inglés | MEDLINE | ID: covidwho-1512696

RESUMEN

Survivors of severe SARS-CoV-2 infections frequently suffer from a range of post-infection sequelae. Whether survivors of mild or asymptomatic infections can expect any long-term health consequences is not yet known. Herein we investigated lasting changes to soluble inflammatory factors and cellular immune phenotype and function in individuals who had recovered from mild SARS-CoV-2 infections (n = 22), compared to those that had recovered from other mild respiratory infections (n = 11). Individuals who had experienced mild SARS-CoV-2 infections had elevated levels of C-reactive protein 1-3 months after symptom onset, and changes in phenotype and function of circulating T-cells that were not apparent in individuals 6-9 months post-symptom onset. Markers of monocyte activation, and expression of adherence and chemokine receptors indicative of altered migratory capacity, were also higher at 1-3 months post-infection in individuals who had mild SARS-CoV-2, but these were no longer elevated by 6-9 months post-infection. Perhaps most surprisingly, significantly more T-cells could be activated by polyclonal stimulation in individuals who had recently experienced a mild SARS-CoV-2, infection compared to individuals with other recent respiratory infections. These data are indicative of prolonged immune activation and systemic inflammation that persists for at least three months after mild or asymptomatic SARS-CoV-2 infections.


Asunto(s)
Infecciones Asintomáticas , COVID-19/inmunología , Citocinas/metabolismo , Leucocitos/inmunología , Leucocitos/metabolismo , Infecciones del Sistema Respiratorio/inmunología , SARS-CoV-2/inmunología , Adulto , Anciano , Anticuerpos Antivirales , Biomarcadores , Proteína C-Reactiva/inmunología , Proteína C-Reactiva/metabolismo , COVID-19/virología , Citocinas/inmunología , Femenino , Humanos , Inmunofenotipificación/métodos , Inflamación/metabolismo , Inflamación/virología , Activación de Linfocitos , Masculino , Persona de Mediana Edad , Infecciones del Sistema Respiratorio/virología , Glicoproteína de la Espiga del Coronavirus/inmunología , Sobrevivientes , Linfocitos T/inmunología , Linfocitos T/metabolismo
2.
Chest ; 158(6): 2270-2274, 2020 12.
Artículo en Inglés | MEDLINE | ID: covidwho-654747
4.
Chest ; 158(3): 1069-1078, 2020 09.
Artículo en Inglés | MEDLINE | ID: covidwho-735016

RESUMEN

The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2, has affected virtually all aspects of patient care. Health-care systems around the world are trying simultaneously to treat patients with COVID-19, prepare for its long-term impacts, and treat patients with other acute and chronic diseases. There are multiple ways that the COVID-19 pandemic will directly affect patients with fibrotic interstitial lung disease (ILD), particularly given their common risk factors for poor outcomes. Major issues for patients with ILD will include restricted access to key components of the diagnostic process, new uncertainties in the use of common ILD pharmacotherapies, limited ability to monitor both disease severity and the presence of medication adverse effects, and significantly curtailed research activities. The purpose of this review is to summarize how COVID-19 has impacted key components of the diagnosis and management of fibrotic ILD as well as to provide strategies to mitigate these challenges. We further review major obstacles for researchers and identify priority areas for future ILD research related to COVID-19. Our goals are to provide practical considerations to support the care of patients with ILD during the COVID-19 pandemic and to provide a road map for clinicians caring for these patients during future infectious disease outbreaks.


Asunto(s)
Betacoronavirus , Infecciones por Coronavirus/complicaciones , Manejo de la Enfermedad , Enfermedades Pulmonares Intersticiales/diagnóstico , Pandemias , Atención al Paciente/métodos , Neumonía Viral/complicaciones , COVID-19 , Infecciones por Coronavirus/epidemiología , Infecciones por Coronavirus/terapia , Humanos , Enfermedades Pulmonares Intersticiales/etiología , Enfermedades Pulmonares Intersticiales/terapia , Neumonía Viral/epidemiología , Neumonía Viral/terapia , Factores de Riesgo , SARS-CoV-2
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