Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range - Winkley, Konner; Banerjee, Dithi; Bradley, Todd; Koseva, Boryana; Cheung, Warren A.; Selvarangan, Rangaraj; Pastinen, Tomi; Grundberg, Elin (Scientific reports, 2021)
Keywords: 631/208/191; 631/250/347; Adolescent; Adult; Age; Antiviral activity; Antiviral drugs; Child; Child, Preschool; COVID-19; COVID-19 - genetics; COVID-19 - immunology; Epithelial cells; Female; Humanities and Social Sciences; Humans; Immune response; Immune system; Immunity, Cellular; Immunity, Innate; Immunization; Infant; Innate immunity; Life span; Lymphocytes T; Male; Middle Aged; Mucosa; multidisciplinary; Nasal Mucosa - cytology; Nasal Mucosa - immunology; Nasal Mucosa - metabolism; Respiratory diseases; SARS-CoV-2 - immunology; Science; Science (multidisciplinary); Severe acute respiratory syndrome coronavirus 2; Severity of Illness Index; T-Lymphocytes - immunology; T-Lymphocytes - metabolism; Transcription; Transcriptome; Young Adult