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The clinical significance of intrahepatic Th22 cells in liver cirrhosis.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University 2019 Februrary 9
BACKGROUND: Th22 cells are a recently identified CD4+ T helper subset and have been implicated in the pathogenesis of certain diseases in humans, but the role of Th22 cells in liver cirrhosis (LC) remains unclear.
OBJECTIVES: The aim of the study was to investigate the expression and clinical significance of intrahepatic Th22 cells in LC tissues.
MATERIAL AND METHODS: Samples of liver tissue of 20 LC patients and 12 normal controls (NC) were collected. Interleukin 22 (IL-22), IL-22R1 mRNA and aryl hydrocarbon receptor (AHR) expression were examined using quantitative reverse transcription polymerase chain reaction (RT-PCR). The protein expression of Th22 and CD4+ cells in liver tissue was measured with immunohistochemistry.
RESULTS: The number of intrahepatic Th22 and CD4+ cells increased markedly in LC patients and the number of Th22 cells positively correlated with the number of CD4+ cells (p < 0.05). Moreover, the number of Th22 cells positively correlated with the serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST), as well as the Child-Pugh score in LC patients (p < 0.05). The expression of IL-22, IL-22R1 and AHR in LC patients was significantly increased compared with the NC group (p < 0.05).
CONCLUSIONS: Our findings suggest that the expression of intrahepatic Th22 cells increased in LC patients and was associated with the progression of LC.
OBJECTIVES: The aim of the study was to investigate the expression and clinical significance of intrahepatic Th22 cells in LC tissues.
MATERIAL AND METHODS: Samples of liver tissue of 20 LC patients and 12 normal controls (NC) were collected. Interleukin 22 (IL-22), IL-22R1 mRNA and aryl hydrocarbon receptor (AHR) expression were examined using quantitative reverse transcription polymerase chain reaction (RT-PCR). The protein expression of Th22 and CD4+ cells in liver tissue was measured with immunohistochemistry.
RESULTS: The number of intrahepatic Th22 and CD4+ cells increased markedly in LC patients and the number of Th22 cells positively correlated with the number of CD4+ cells (p < 0.05). Moreover, the number of Th22 cells positively correlated with the serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST), as well as the Child-Pugh score in LC patients (p < 0.05). The expression of IL-22, IL-22R1 and AHR in LC patients was significantly increased compared with the NC group (p < 0.05).
CONCLUSIONS: Our findings suggest that the expression of intrahepatic Th22 cells increased in LC patients and was associated with the progression of LC.
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