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10.3389/fimmu.2022.903498

http://scihub22266oqcxt.onion/10.3389/fimmu.2022.903498
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35711451!9196331!35711451
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suck abstract from ncbi


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pmid35711451      Front+Immunol 2022 ; 13 (ä): 903498
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  • Autophagy Hijacking in PBMC From COVID-19 Patients Results in Lymphopenia #MMPMID35711451
  • Barbati C; Celia AI; Colasanti T; Vomero M; Speziali M; Putro E; Buoncuore G; Savino F; Colafrancesco S; Ucci FM; Ciancarella C; Balbinot E; Scarpa S; Natalucci F; Pellegrino G; Ceccarelli F; Spinelli FR; Mastroianni CM; Conti F; Alessandri C
  • Front Immunol 2022[]; 13 (ä): 903498 PMID35711451show ga
  • Autophagy is a homeostatic process responsible for the self-digestion of intracellular components and antimicrobial defense by inducing the degradation of pathogens into autophagolysosomes. Recent findings suggest an involvement of this process in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. However, the role of autophagy in the immunological mechanisms of coronavirus disease 2019 (COVID-19) pathogenesis remains largely unexplored. This study reveals the presence of autophagy defects in peripheral immune cells from COVID-19 patients. The impairment of the autophagy process resulted in a higher percentage of lymphocytes undergoing apoptosis in COVID-19 patients. Moreover, the inverse correlation between autophagy markers levels and peripheral lymphocyte counts in COVID-19 patients confirms how a defect in autophagy might contribute to lymphopenia, causing a reduction in the activation of viral defense. These results provided intriguing data that could help in understanding the cellular underlying mechanisms in COVID-19 infection, especially in severe forms.
  • |*COVID-19[MESH]
  • |*Lymphopenia[MESH]
  • |Autophagy[MESH]
  • |Humans[MESH]
  • |Leukocytes, Mononuclear[MESH]


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