دورية أكاديمية

Maturation signatures of conventional dendritic cell subtypes in COVID‐19 suggest direct viral sensing

التفاصيل البيبلوغرافية
العنوان: Maturation signatures of conventional dendritic cell subtypes in COVID‐19 suggest direct viral sensing
المؤلفون: Marongiu, Laura, Protti, Giulia, Facchini, Fabio A., Valache, Mihai, Mingozzi, Francesca, Ranzani, Valeria, Putignano, Anna Rita, Salviati, Lorenzo, Bevilacqua, Valeria, Curti, Serena, Crosti, Mariacristina, Sarnicola, Maria Lucia, D'Angiò, Mariella, Bettini, Laura Rachele, Biondi, Andrea, Nespoli, Luca, Tamini, Nicolò, Clementi, Nicola, Mancini, Nicasio, Abrignani, Sergio, Spreafico, Roberto, Granucci, Francesca
المساهمون: Marongiu, Laura, Protti, Giulia, Facchini, Fabio A., Valache, Mihai, Mingozzi, Francesca, Ranzani, Valeria, Putignano, Anna Rita, Salviati, Lorenzo, Bevilacqua, Valeria, Curti, Serena, Crosti, Mariacristina, Sarnicola, Maria Lucia, D'Angiò, Mariella, Bettini, Laura Rachele, Biondi, Andrea, Nespoli, Luca, Tamini, Nicolò, Clementi, Nicola, Mancini, Nicasio, Abrignani, Sergio, Spreafico, Roberto, Granucci, Francesca
سنة النشر: 2022
المجموعة: IRInSubria - Institutional Repository Insubria (Università degli Studi dell’Insubria)
مصطلحات موضوعية: COVID-19, dendritic cells, single cell transcriptomics
الوصف: Growing evidence suggests that conventional dendritic cells (cDCs) undergo aberrant maturation in COVID-19, which negatively affects T-cell activation. The presence of effector T cells in patients with mild disease and dysfunctional T cells in severely ill patients suggests that adequate T-cell responses limit disease severity. Understanding how cDCs cope with SARS-CoV-2 can help elucidate how protective immune responses are generated. Here, we report that cDC2 subtypes exhibit similar infection-induced gene signatures, with the upregulation of interferon-stimulated genes and interleukin (IL)-6 signaling pathways. Furthermore, comparison of cDCs between patients with severe and mild disease showed severely ill patients to exhibit profound downregulation of genes encoding molecules involved in antigen presentation, such as MHCII, TAP, and costimulatory proteins, whereas we observed the opposite for proinflammatory molecules, such as complement and coagulation factors. Thus, as disease severity increases, cDC2s exhibit enhanced inflammatory properties and lose antigen presentation capacity. Moreover, DC3s showed upregulation of anti-apoptotic genes and accumulated during infection. Direct exposure of cDC2s to the virus in vitro recapitulated the activation profile observed in vivo. Our findings suggest that SARS-CoV-2 interacts directly with cDC2s and implements an efficient immune escape mechanism that correlates with disease severity by downregulating crucial molecules required for T-cell activation.
نوع الوثيقة: article in journal/newspaper
وصف الملف: ELETTRONICO
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34333764; info:eu-repo/semantics/altIdentifier/wos/WOS:000702439500001; volume:52; issue:1; firstpage:109; lastpage:122; numberofpages:14; journal:EUROPEAN JOURNAL OF IMMUNOLOGY; https://hdl.handle.net/11383/2148967Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85114479544
DOI: 10.1002/eji.202149298
الإتاحة: https://doi.org/10.1002/eji.202149298Test
https://hdl.handle.net/11383/2148967Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.312CD2E8
قاعدة البيانات: BASE