Concept
Upregulation of Pulmonary Immune Cell-Derived Ligands from SARS-CoV-2 Infection.
Various genes have shown to be differentially expressed in COVID-19 patient bronchial alveolar lavage fluid (BALF) as compared to control data. The following list includes upregulated genes involved in known, clinical characterizations of COVID-19.
- cytokine storm ( CCL2/3/4/7/8, CXCL1/2/6/8/28, CCL3L3, CCL4L2)
- hypoxia (HIF1A, HLF)
- inflammasome /sepsis (IL1R1/2, IL5RA, IL33, IL31RA)
Immunity markers:
- alveolar cells (EHF, PAX9, ELF3, GHRL2)
- immune cells (RFX3, SOX5, TP63, HOPX)
- antiviral regulation (NR3C2)
- lymphocyte B cells (CD24 and CD38)
- lymphocyte T cells (CD4, CD8) (detected but not consistently upregulated)
Notable upregulated genes:
- Cytokines
- Epiregulin (EREG)
- Eph ligand genes (EFNA1, EFNA5)
0
1
Updated 2020-07-23
Tags
SARS-CoV-2 (COVID-19)
Biomedical Sciences
Related
Upregulation of Pulmonary Immune Cell-Derived Ligands from SARS-CoV-2 Infection.
Sensory Neurons Express Receptors for Immune Factors Upregulated from SARS-CoV-2 Infection
Figure: Chronology of events during SARS-CoV-2 infection.
Upregulation of Pulmonary Immune Cell-Derived Ligands from SARS-CoV-2 Infection.