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Kir Variation in Iranians Combines High Haplotype and Allotype Diversity With an Abundance of Functional Inhibitory Receptors Publisher Pubmed



Alicata C1 ; Ashouri E2, 3, 4, 5 ; Nematgorgani N2, 3, 6 ; Guethlein LA2, 3 ; Marin WM7 ; Tao S8, 9 ; Moretta L1 ; Hollenbach JA7 ; Trowsdale J6 ; Traherne JA6 ; Ghaderi A5 ; Parham P2, 3 ; Norman PJ2, 3, 9
Authors
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Authors Affiliations
  1. 1. Department of Immunology, IRCCS Bambino Gesu Children's Hospital, Rome, Italy
  2. 2. Department of Structural Biology, Stanford University School of Medicine, Stanford, CA, United States
  3. 3. Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, United States
  4. 4. Hematology-Oncology and Stem Cell Transplantation Research Center, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. School of Medicine, Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran
  6. 6. Division of Immunology, Department of Pathology, University of Cambridge, Cambridge, United Kingdom
  7. 7. Department of Neurology, University of California, San Francisco, San Francisco, CA, United States
  8. 8. Blood Center of Zhejiang Province, Hangzhou, China
  9. 9. Division of Personalized Medicine, Department of Immunology and Microbiology, University of Colorado, Anschutz Medical Campus, Aurora, CO, United States

Source: Frontiers in Immunology Published:2020


Abstract

Natural killer (NK) cells are innate lymphocytes that eliminate infected and transformed cells. They discriminate healthy from diseased tissue through killer cell Ig-like receptor (KIR) recognition of HLA class I ligands. Directly impacting NK cell function, KIR polymorphism associates with infection control and multiple autoimmune and pregnancy syndromes. Here we analyze KIR diversity of 241 individuals from five groups of Iranians. These five populations represent Baloch, Kurd, and Lur, together comprising 15% of the ethnically diverse Iranian population. We identified 159 KIR alleles, including 11 not previously characterized. We also identified 170 centromeric and 94 telomeric haplotypes, and 15 different KIR haplotypes carrying either a deletion or duplication encompassing one or more complete KIR genes. As expected, comparing our data with those representing major worldwide populations revealed the greatest similarity between Iranians and Europeans. Despite this similarity we observed higher frequencies of KIR3DL1*001 in Iran than any other population, and the highest frequency of HLA-B*51, a Bw4-containing allotype that acts as a strong educator of KIR3DL1*001+ NK cells. Compared to Europeans, the Iranians we studied also have a reduced frequency of 3DL1*004, which encodes an allotype that is not expressed at the NK cell surface. Concurrent with the resulting high frequency of strong viable interactions between inhibitory KIR and polymorphic HLA class I, the majority of KIR-A haplotypes characterized do not express a functional activating receptor. By contrast, the most frequent KIR-B haplotype in Iran expresses only one functional inhibitory KIR and the maximum number of activating KIR. This first complete, high-resolution, characterization of the KIR locus of Iranians will form a valuable reference for future clinical and population studies. © Copyright © 2020 Alicata, Ashouri, Nemat-Gorgani, Guethlein, Marin, Tao, Moretta, Hollenbach, Trowsdale, Traherne, Ghaderi, Parham and Norman.
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