Expression of AXL receptor tyrosine kinase relates to monocyte dysfunction and severity of cirrhosis
Research output: Contribution to journal › Article
Colleges, School and Institutes
- Medical Research Centre and Division of Gastroenterology and Hepatology
- King's Health Partners Cancer Biobank, King's College London, London, UK.
- Department of Life Sciences, Imperial College London, London, UK
- University of Basel and University Centre for Gastrointestinal and Liver Diseases
- Institute of Immunobiology, Kantonsspital St. Gallen , St. Gallen , Switzerland.
- Imperial College London
Infectious complications in patients with cirrhosis frequently initiate episodes of decompensation and substantially contribute to the high mortality. Mechanisms of the underlying immuneparesis remain underexplored. TAM receptors (TYRO3/AXL/MERTK) are important inhibitors of innate immune responses. To understand the pathophysiology of immuneparesis in cirrhosis, we detailed TAM receptor expression in relation to monocyte function and disease severity prior to the onset of acute decompensation. TNF-α/IL-6 responses to lipopolysaccharide were attenuated in monocytes from patients with cirrhosis (n = 96) compared with controls (n = 27) and decreased in parallel with disease severity. Concurrently, an AXL-expressing (AXL+) monocyte population expanded. AXL+ cells (CD14+CD16highHLA-DRhigh) were characterised by attenuated TNF-α/IL-6 responses and T cell activation but enhanced efferocytosis and preserved phagocytosis of Escherichia coli Their expansion correlated with disease severity, complications, infection, and 1-yr mortality. AXL+ monocytes were generated in response to microbial products and efferocytosis in vitro. AXL kinase inhibition and down-regulation reversed attenuated monocyte inflammatory responses in cirrhosis ex vivo. AXL may thus serve as prognostic marker and deserves evaluation as immunotherapeutic target in cirrhosis.
|Number of pages||16|
|Journal||Life Science Alliance|
|Early online date||10 Dec 2019|
|Publication status||Published - Jan 2020|