Abstract

BackgroundNatural killer cells are involved in the complex mechanisms underlying autoimmune diseases but few studies have investigated their role in autoimmune hepatitis. Killer immunoglobulin-like receptors are key regulators of natural killer cell-mediated immune responses.Methods and FindingsKIR gene frequencies, KIR haplotypes, KIR ligands and combinations of KIRs and their HLA Class I ligands were investigated in 114 patients diagnosed with type 1 autoimmune hepatitis and compared with a group of 221 healthy controls. HLA Class I and Class II antigen frequencies were compared to those of 551 healthy unrelated families representative of the Sardinian population. In our cohort, type 1 autoimmune hepatitis was strongly associated with the HLA-B18, Cw5, DR3 haplotype. The KIR2DS1 activating KIR gene and the high affinity HLA-C2 ligands were significantly higher in patients compared to controls. Patients also had a reduced frequency of HLA-Bw4 ligands for KIR3DL1 and HLA-C1 ligands for KIR2DL3. Age at onset was significantly associated with the KIR2DS1 activating gene but not with HLA-C1 or HLA-C2 ligand groups.ConclusionsThe activating KIR gene KIR2DS1 resulted to have an important predictive potential for early onset of type 1 autoimmune hepatitis. Additionally, the low frequency of the KIR-ligand combinations KIR3DL1/HLA-Bw4 and KIR2DL3/HLA-C1 coupled to the high frequency of the HLA-C2 high affinity ligands for KIR2DS1 could contribute to unwanted NK cell autoreactivity in AIH-1.

Highlights

  • Autoimmune hepatitis (AIH) is a rare chronic liver disorder [1] characterized by loss of immunological tolerance to autologous liver tissue

  • The diagnosis of AIH is primarily based on the scoring system established by the International Autoimmune Hepatitis Group (IAIHG) in 1993 and revised in 1999 [5]

  • Updated diagnostic and treatment strategies are published in the guidelines of the American Association for the Study of Liver Diseases (AASLD)

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Summary

Introduction

Autoimmune hepatitis (AIH) is a rare chronic liver disorder [1] characterized by loss of immunological tolerance to autologous liver tissue. This breakage in the immune system typically causes hepatocellular inflammation with high levels of circulating autoantibodies, hypergammaglobulinemia and fluctuating increases of serum transaminases and immunoglobulin G levels. The diagnosis of AIH is primarily based on the scoring system established by the International Autoimmune Hepatitis Group (IAIHG) in 1993 and revised in 1999 [5]. Natural killer cells are involved in the complex mechanisms underlying autoimmune diseases but few studies have investigated their role in autoimmune hepatitis. Killer immunoglobulin-like receptors are key regulators of natural killer cell-mediated immune responses

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