PLoS ONE (Jan 2016)

Exploring the Role of Killer Cell Immunoglobulin-Like Receptors and Their HLA Class I Ligands in Autoimmune Hepatitis.

  • Roberto Littera,
  • Luchino Chessa,
  • Simona Onali,
  • Francesco Figorilli,
  • Sara Lai,
  • Luca Secci,
  • Giorgio La Nasa,
  • Giovanni Caocci,
  • Marcella Arras,
  • Maurizio Melis,
  • Sara Cappellini,
  • Cinzia Balestrieri,
  • Giancarlo Serra,
  • Maria Conti,
  • Teresa Zolfino,
  • Michele Casale,
  • Stefania Casu,
  • Maria Cristina Pasetto,
  • Lucia Barca,
  • Claudia Salustro,
  • Laura Matta,
  • Rosetta Scioscia,
  • Fausto Zamboni,
  • Gavino Faa,
  • Sandro Orrù,
  • Carlo Carcassi

DOI
https://doi.org/10.1371/journal.pone.0146086
Journal volume & issue
Vol. 11, no. 1
p. e0146086

Abstract

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BACKGROUND: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. METHODS AND FINDINGS:KIR 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. CONCLUSIONS:The 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.