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Rev Iberoam Micol ; 37(2): 41-46, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33041191

RESUMEN

Critically ill COVID-19 patients have higher pro-inflammatory (IL-1, IL-2, IL-6, tumor necrosis alpha) and anti-inflammatory (IL-4, IL-10) cytokine levels, less CD4 interferon-gamma expression, and fewer CD4 and CD8 cells. This severe clinical situation increases the risk of serious fungal infections, such as invasive pulmonary aspergillosis, invasive candidiasis or Pneumocystis jirovecii pneumonia. However, few studies have investigated fungal coinfections in this population. We describe an update on published reports on fungal coinfections and our personal experience in three Spanish hospitals. We can conclude that despite the serious disease caused by SARS-CoV-2 in many patients, the scarcity of invasive mycoses is probably due to the few bronchoscopies and necropsies performed in these patients because of the high risk in aerosol generation. However, the presence of fungal markers in clinically relevant specimens, with the exception of bronchopulmonary colonization by Candida, should make it advisable to early implement antifungal therapy.


Asunto(s)
Betacoronavirus , Candidiasis Invasiva/epidemiología , Coinfección/epidemiología , Infecciones por Coronavirus/epidemiología , Aspergilosis Pulmonar Invasiva/epidemiología , Neumonía por Pneumocystis/epidemiología , Neumonía Viral/epidemiología , Linfocitos T CD4-Positivos , Linfocitos T CD8-positivos , COVID-19 , Infecciones por Coronavirus/sangre , Humanos , Interferón gamma/sangre , Interleucinas/sangre , Pandemias , Neumonía Viral/sangre , SARS-CoV-2 , España/epidemiología , Factor de Necrosis Tumoral alfa/sangre
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