Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy
Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to...
Ausführliche Beschreibung
Autor*in: |
Calvo-Alvarez, Estefanía [verfasserIn] D’Alessandro, Sarah [verfasserIn] Zanotta, Nunzia [verfasserIn] Basilico, Nicoletta [verfasserIn] Parapini, Silvia [verfasserIn] Signorini, Lucia [verfasserIn] Perego, Federica [verfasserIn] Maina, Kevin Kamau [verfasserIn] Ferrante, Pasquale [verfasserIn] Modenese, Annalisa [verfasserIn] Pizzocri, Pierluigi [verfasserIn] Ronsivalle, Andrea [verfasserIn] Delbue, Serena [verfasserIn] Comar, Manola [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2024 |
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Schlagwörter: |
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Anmerkung: |
© The Author(s) 2024 |
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Übergeordnetes Werk: |
Enthalten in: BMC immunology - BioMed Central, 2000, 25(2024), 1 vom: 26. Juli |
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Übergeordnetes Werk: |
volume:25 ; year:2024 ; number:1 ; day:26 ; month:07 |
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DOI / URN: |
10.1186/s12865-024-00641-z |
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Katalog-ID: |
SPR056739176 |
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245 | 1 | 0 | |a Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy |
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520 | |a Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. | ||
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650 | 4 | |a Primarily-infected subjects |7 (dpeaa)DE-He213 | |
650 | 4 | |a Serum cytokine/chemokines levels |7 (dpeaa)DE-He213 | |
650 | 4 | |a Anti-SARS-CoV-2 IgG |7 (dpeaa)DE-He213 | |
700 | 1 | |a D’Alessandro, Sarah |e verfasserin |4 aut | |
700 | 1 | |a Zanotta, Nunzia |e verfasserin |4 aut | |
700 | 1 | |a Basilico, Nicoletta |e verfasserin |4 aut | |
700 | 1 | |a Parapini, Silvia |e verfasserin |4 aut | |
700 | 1 | |a Signorini, Lucia |e verfasserin |4 aut | |
700 | 1 | |a Perego, Federica |e verfasserin |4 aut | |
700 | 1 | |a Maina, Kevin Kamau |e verfasserin |4 aut | |
700 | 1 | |a Ferrante, Pasquale |e verfasserin |4 aut | |
700 | 1 | |a Modenese, Annalisa |e verfasserin |4 aut | |
700 | 1 | |a Pizzocri, Pierluigi |e verfasserin |4 aut | |
700 | 1 | |a Ronsivalle, Andrea |e verfasserin |4 aut | |
700 | 1 | |a Delbue, Serena |e verfasserin |4 aut | |
700 | 1 | |a Comar, Manola |e verfasserin |4 aut | |
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10.1186/s12865-024-00641-z doi (DE-627)SPR056739176 (SPR)s12865-024-00641-z-e DE-627 ger DE-627 rakwb eng 610 VZ 44.45 bkl Calvo-Alvarez, Estefanía verfasserin aut Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. COVID-19 (dpeaa)DE-He213 SARS-CoV-2 (dpeaa)DE-He213 Primarily-infected subjects (dpeaa)DE-He213 Serum cytokine/chemokines levels (dpeaa)DE-He213 Anti-SARS-CoV-2 IgG (dpeaa)DE-He213 D’Alessandro, Sarah verfasserin aut Zanotta, Nunzia verfasserin aut Basilico, Nicoletta verfasserin aut Parapini, Silvia verfasserin aut Signorini, Lucia verfasserin aut Perego, Federica verfasserin aut Maina, Kevin Kamau verfasserin aut Ferrante, Pasquale verfasserin aut Modenese, Annalisa verfasserin aut Pizzocri, Pierluigi verfasserin aut Ronsivalle, Andrea verfasserin aut Delbue, Serena verfasserin aut Comar, Manola verfasserin aut Enthalten in BMC immunology BioMed Central, 2000 25(2024), 1 vom: 26. Juli (DE-627)326644962 (DE-600)2041500-X 1471-2172 nnns volume:25 year:2024 number:1 day:26 month:07 https://dx.doi.org/10.1186/s12865-024-00641-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 44.45 VZ AR 25 2024 1 26 07 |
spelling |
10.1186/s12865-024-00641-z doi (DE-627)SPR056739176 (SPR)s12865-024-00641-z-e DE-627 ger DE-627 rakwb eng 610 VZ 44.45 bkl Calvo-Alvarez, Estefanía verfasserin aut Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. COVID-19 (dpeaa)DE-He213 SARS-CoV-2 (dpeaa)DE-He213 Primarily-infected subjects (dpeaa)DE-He213 Serum cytokine/chemokines levels (dpeaa)DE-He213 Anti-SARS-CoV-2 IgG (dpeaa)DE-He213 D’Alessandro, Sarah verfasserin aut Zanotta, Nunzia verfasserin aut Basilico, Nicoletta verfasserin aut Parapini, Silvia verfasserin aut Signorini, Lucia verfasserin aut Perego, Federica verfasserin aut Maina, Kevin Kamau verfasserin aut Ferrante, Pasquale verfasserin aut Modenese, Annalisa verfasserin aut Pizzocri, Pierluigi verfasserin aut Ronsivalle, Andrea verfasserin aut Delbue, Serena verfasserin aut Comar, Manola verfasserin aut Enthalten in BMC immunology BioMed Central, 2000 25(2024), 1 vom: 26. Juli (DE-627)326644962 (DE-600)2041500-X 1471-2172 nnns volume:25 year:2024 number:1 day:26 month:07 https://dx.doi.org/10.1186/s12865-024-00641-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 44.45 VZ AR 25 2024 1 26 07 |
allfields_unstemmed |
10.1186/s12865-024-00641-z doi (DE-627)SPR056739176 (SPR)s12865-024-00641-z-e DE-627 ger DE-627 rakwb eng 610 VZ 44.45 bkl Calvo-Alvarez, Estefanía verfasserin aut Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. COVID-19 (dpeaa)DE-He213 SARS-CoV-2 (dpeaa)DE-He213 Primarily-infected subjects (dpeaa)DE-He213 Serum cytokine/chemokines levels (dpeaa)DE-He213 Anti-SARS-CoV-2 IgG (dpeaa)DE-He213 D’Alessandro, Sarah verfasserin aut Zanotta, Nunzia verfasserin aut Basilico, Nicoletta verfasserin aut Parapini, Silvia verfasserin aut Signorini, Lucia verfasserin aut Perego, Federica verfasserin aut Maina, Kevin Kamau verfasserin aut Ferrante, Pasquale verfasserin aut Modenese, Annalisa verfasserin aut Pizzocri, Pierluigi verfasserin aut Ronsivalle, Andrea verfasserin aut Delbue, Serena verfasserin aut Comar, Manola verfasserin aut Enthalten in BMC immunology BioMed Central, 2000 25(2024), 1 vom: 26. Juli (DE-627)326644962 (DE-600)2041500-X 1471-2172 nnns volume:25 year:2024 number:1 day:26 month:07 https://dx.doi.org/10.1186/s12865-024-00641-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 44.45 VZ AR 25 2024 1 26 07 |
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10.1186/s12865-024-00641-z doi (DE-627)SPR056739176 (SPR)s12865-024-00641-z-e DE-627 ger DE-627 rakwb eng 610 VZ 44.45 bkl Calvo-Alvarez, Estefanía verfasserin aut Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. COVID-19 (dpeaa)DE-He213 SARS-CoV-2 (dpeaa)DE-He213 Primarily-infected subjects (dpeaa)DE-He213 Serum cytokine/chemokines levels (dpeaa)DE-He213 Anti-SARS-CoV-2 IgG (dpeaa)DE-He213 D’Alessandro, Sarah verfasserin aut Zanotta, Nunzia verfasserin aut Basilico, Nicoletta verfasserin aut Parapini, Silvia verfasserin aut Signorini, Lucia verfasserin aut Perego, Federica verfasserin aut Maina, Kevin Kamau verfasserin aut Ferrante, Pasquale verfasserin aut Modenese, Annalisa verfasserin aut Pizzocri, Pierluigi verfasserin aut Ronsivalle, Andrea verfasserin aut Delbue, Serena verfasserin aut Comar, Manola verfasserin aut Enthalten in BMC immunology BioMed Central, 2000 25(2024), 1 vom: 26. Juli (DE-627)326644962 (DE-600)2041500-X 1471-2172 nnns volume:25 year:2024 number:1 day:26 month:07 https://dx.doi.org/10.1186/s12865-024-00641-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 44.45 VZ AR 25 2024 1 26 07 |
allfieldsSound |
10.1186/s12865-024-00641-z doi (DE-627)SPR056739176 (SPR)s12865-024-00641-z-e DE-627 ger DE-627 rakwb eng 610 VZ 44.45 bkl Calvo-Alvarez, Estefanía verfasserin aut Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s) 2024 Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. COVID-19 (dpeaa)DE-He213 SARS-CoV-2 (dpeaa)DE-He213 Primarily-infected subjects (dpeaa)DE-He213 Serum cytokine/chemokines levels (dpeaa)DE-He213 Anti-SARS-CoV-2 IgG (dpeaa)DE-He213 D’Alessandro, Sarah verfasserin aut Zanotta, Nunzia verfasserin aut Basilico, Nicoletta verfasserin aut Parapini, Silvia verfasserin aut Signorini, Lucia verfasserin aut Perego, Federica verfasserin aut Maina, Kevin Kamau verfasserin aut Ferrante, Pasquale verfasserin aut Modenese, Annalisa verfasserin aut Pizzocri, Pierluigi verfasserin aut Ronsivalle, Andrea verfasserin aut Delbue, Serena verfasserin aut Comar, Manola verfasserin aut Enthalten in BMC immunology BioMed Central, 2000 25(2024), 1 vom: 26. Juli (DE-627)326644962 (DE-600)2041500-X 1471-2172 nnns volume:25 year:2024 number:1 day:26 month:07 https://dx.doi.org/10.1186/s12865-024-00641-z X:SPRINGER Resolving-System kostenfrei Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 44.45 VZ AR 25 2024 1 26 07 |
language |
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source |
Enthalten in BMC immunology 25(2024), 1 vom: 26. Juli volume:25 year:2024 number:1 day:26 month:07 |
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Enthalten in BMC immunology 25(2024), 1 vom: 26. Juli volume:25 year:2024 number:1 day:26 month:07 |
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COVID-19 SARS-CoV-2 Primarily-infected subjects Serum cytokine/chemokines levels Anti-SARS-CoV-2 IgG |
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BMC immunology |
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Calvo-Alvarez, Estefanía @@aut@@ D’Alessandro, Sarah @@aut@@ Zanotta, Nunzia @@aut@@ Basilico, Nicoletta @@aut@@ Parapini, Silvia @@aut@@ Signorini, Lucia @@aut@@ Perego, Federica @@aut@@ Maina, Kevin Kamau @@aut@@ Ferrante, Pasquale @@aut@@ Modenese, Annalisa @@aut@@ Pizzocri, Pierluigi @@aut@@ Ronsivalle, Andrea @@aut@@ Delbue, Serena @@aut@@ Comar, Manola @@aut@@ |
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2024-07-26T00:00:00Z |
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Calvo-Alvarez, Estefanía D’Alessandro, Sarah Zanotta, Nunzia Basilico, Nicoletta Parapini, Silvia Signorini, Lucia Perego, Federica Maina, Kevin Kamau Ferrante, Pasquale Modenese, Annalisa Pizzocri, Pierluigi Ronsivalle, Andrea Delbue, Serena Comar, Manola |
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multiplex array analysis of circulating cytokines and chemokines in covid-19 patients during the first wave of the sars-cov-2 pandemic in milan, italy |
title_auth |
Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy |
abstract |
Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. © The Author(s) 2024 |
abstractGer |
Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. © The Author(s) 2024 |
abstract_unstemmed |
Background The systemic inflammatory syndrome called “cytokine storm” has been described in COVID-19 pathogenesis, contributing to disease severity. The analysis of cytokine and chemokine levels in the blood of 21 SARS-CoV-2 positive patients throughout the phases of the pandemic has been studied to understand immune response dysregulation and identify potential disease biomarkers for new treatments. The present work reports the cytokine and chemokine levels in sera from a small cohort of individuals primarily infected with SARS-CoV-2 during the first wave of the COVID-19 pandemic in Milan (Italy). Results Among the 27 cytokines and chemokines investigated, a significant higher expression of Interleukin-9 (IL-9), IP-10 (CXCL10), MCP-1 (CCL2) and RANTES (CCL-5) in infected patients compared to uninfected subjects was observed. When the change in cytokine/chemokine levels was monitored over time, from the hospitalization day to discharge, only IL-6 and IP-10 showed a significant decrease. Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. Consequently, the immunological features and dynamic cytokine profiles of non-vaccinated and primarily-infected subjects reported here provide novel insights into the inflammatory immune landscape in the context of SARS-CoV-2 infection, and offer valuable knowledge for addressing future viral infections and the development of novel treatments. © The Author(s) 2024 |
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Multiplex array analysis of circulating cytokines and chemokines in COVID-19 patients during the first wave of the SARS-CoV-2 pandemic in Milan, Italy |
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https://dx.doi.org/10.1186/s12865-024-00641-z |
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D’Alessandro, Sarah Zanotta, Nunzia Basilico, Nicoletta Parapini, Silvia Signorini, Lucia Perego, Federica Maina, Kevin Kamau Ferrante, Pasquale Modenese, Annalisa Pizzocri, Pierluigi Ronsivalle, Andrea Delbue, Serena Comar, Manola |
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D’Alessandro, Sarah Zanotta, Nunzia Basilico, Nicoletta Parapini, Silvia Signorini, Lucia Perego, Federica Maina, Kevin Kamau Ferrante, Pasquale Modenese, Annalisa Pizzocri, Pierluigi Ronsivalle, Andrea Delbue, Serena Comar, Manola |
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Consistent with these findings, a significant negative correlation was observed between IP-10 and anti-Spike IgG antibodies in infected individuals. In contrast, IL-17 was positively correlated with the production of IgG against SARS-CoV-2. Conclusions The cytokine storm and the modulation of cytokine levels by SARS-CoV-2 infection are hallmarks of COVID-19. The current global immunity profile largely stems from widespread vaccination campaigns and previous infection exposures. 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