tetano
Editor, Senior Moderator
Cell Rep
. 2024 Nov 1;43(11):114900.
doi: 10.1016/j.celrep.2024.114900. Online ahead of print. Serum proteome reveals distinctive molecular features of H7N9- and SARS-CoV-2-infected patients
Yunzhi Wang[SUP] 1 [/SUP], Zhigang Song[SUP] 2 [/SUP], Peng Ran[SUP] 1 [/SUP], Hang Xiang[SUP] 3 [/SUP], Ziyan Xu[SUP] 3 [/SUP], Ning Xu[SUP] 3 [/SUP], Mengjie Deng[SUP] 4 [/SUP], Lingli Zhu[SUP] 3 [/SUP], Yanan Yin[SUP] 3 [/SUP], Jinwen Feng[SUP] 3 [/SUP], Chen Ding[SUP] 5 [/SUP], Wenjun Yang[SUP] 6 [/SUP]
Affiliations
The coronavirus disease 2019 (COVID-19) pandemic has reminded us of human infections with the H7N9 virus and has raised questions related to the clinical and molecular pathophysiological diversity between the two diseases. Here, we performed a proteomic approach on sera samples from patients with H7N9-virus or SARS-CoV-2-virus infection and healthy controls. Compared to SARS-CoV-2, H7N9-virus infection caused elevated neutrophil concentrations, T cell exhaustion, and increased cytokine/interleukin secretion. Cell-type deconvolution and temporal analysis revealed that T cells and neutrophils could regulate the core immunological trajectory and influence the prognosis of patients with severe H7N9-virus infection. Elevated tissue-enhanced proteins combined with alterations of clinical biochemical indexes suggested that H7N9 infection induced more severe inflammatory organ injury and dysfunction in the liver and intestine. Further mechanical analysis revealed that the high concentration of neutrophils might impact the intestinal enterocyte cells through cytokine-receptor interaction, leading to intestinal damage in patients with H7N9-virus infection.
Keywords: CP: Immunology; H7N9 virus; SARS-CoV-2 virus; proteomics.
. 2024 Nov 1;43(11):114900.
doi: 10.1016/j.celrep.2024.114900. Online ahead of print. Serum proteome reveals distinctive molecular features of H7N9- and SARS-CoV-2-infected patients
Yunzhi Wang[SUP] 1 [/SUP], Zhigang Song[SUP] 2 [/SUP], Peng Ran[SUP] 1 [/SUP], Hang Xiang[SUP] 3 [/SUP], Ziyan Xu[SUP] 3 [/SUP], Ning Xu[SUP] 3 [/SUP], Mengjie Deng[SUP] 4 [/SUP], Lingli Zhu[SUP] 3 [/SUP], Yanan Yin[SUP] 3 [/SUP], Jinwen Feng[SUP] 3 [/SUP], Chen Ding[SUP] 5 [/SUP], Wenjun Yang[SUP] 6 [/SUP]
Affiliations
- PMID: 39487987
- DOI: 10.1016/j.celrep.2024.114900
The coronavirus disease 2019 (COVID-19) pandemic has reminded us of human infections with the H7N9 virus and has raised questions related to the clinical and molecular pathophysiological diversity between the two diseases. Here, we performed a proteomic approach on sera samples from patients with H7N9-virus or SARS-CoV-2-virus infection and healthy controls. Compared to SARS-CoV-2, H7N9-virus infection caused elevated neutrophil concentrations, T cell exhaustion, and increased cytokine/interleukin secretion. Cell-type deconvolution and temporal analysis revealed that T cells and neutrophils could regulate the core immunological trajectory and influence the prognosis of patients with severe H7N9-virus infection. Elevated tissue-enhanced proteins combined with alterations of clinical biochemical indexes suggested that H7N9 infection induced more severe inflammatory organ injury and dysfunction in the liver and intestine. Further mechanical analysis revealed that the high concentration of neutrophils might impact the intestinal enterocyte cells through cytokine-receptor interaction, leading to intestinal damage in patients with H7N9-virus infection.
Keywords: CP: Immunology; H7N9 virus; SARS-CoV-2 virus; proteomics.