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10.1016/j.immuni.2022.04.013

http://scihub22266oqcxt.onion/10.1016/j.immuni.2022.04.013
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suck abstract from ncbi


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pmid35545027      Immunity 2022 ; 55 (5): 749-780
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  • Mucosal immune responses to infection and vaccination in the respiratory tract #MMPMID35545027
  • Mettelman RC; Allen EK; Thomas PG
  • Immunity 2022[May]; 55 (5): 749-780 PMID35545027show ga
  • The lungs are constantly exposed to inhaled debris, allergens, pollutants, commensal or pathogenic microorganisms, and respiratory viruses. As a result, innate and adaptive immune responses in the respiratory tract are tightly regulated and are in continual flux between states of enhanced pathogen clearance, immune-modulation, and tissue repair. New single-cell-sequencing techniques are expanding our knowledge of airway cellular complexity and the nuanced connections between structural and immune cell compartments. Understanding these varied interactions is critical in treatment of human pulmonary disease and infections and in next-generation vaccine design. Here, we review the innate and adaptive immune responses in the lung and airways following infection and vaccination, with particular focus on influenza virus and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The ongoing SARS-CoV-2 pandemic has put pulmonary research firmly into the global spotlight, challenging previously held notions of respiratory immunity and helping identify new populations at high risk for respiratory distress.
  • |*COVID-19/prevention & control[MESH]
  • |*SARS-CoV-2[MESH]
  • |Humans[MESH]
  • |Immunity, Innate[MESH]
  • |Immunity, Mucosal[MESH]
  • |Lung[MESH]


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