Analysis of HLA haplotypes in autoimmune hepatitis type 1: identifying the major susceptibility locus
Susceptibility to autoimmune hepatitis type I (AIH-1) has been associated with HLA-DR3, DR52, and DR4 antigens in Caucasian and Oriental patients. However, in Brazil, disease susceptibility is primarily linked to DR13 and DR52. In this highly admixed population, we find different DR13-associated hap...
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Veröffentlicht in: | Human immunology 2001-02, Vol.62 (2), p.165-169 |
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creator | Goldberg, Anna Carla Bittencourt, Paulo L Mougin, Bruno Cançado, Eduardo L.R Porta, Gilda Carrilho, Flair Kalil, Jorge |
description | Susceptibility to autoimmune hepatitis type I (AIH-1) has been associated with HLA-DR3, DR52, and DR4 antigens in Caucasian and Oriental patients. However, in Brazil, disease susceptibility is primarily linked to DR13 and DR52. In this highly admixed population, we find different DR13-associated haplotypes, presenting a unique opportunity to discriminate relevant genes within a tightly linked genomic region. To identify the primary susceptibility locus, we sequenced DR13 alleles of 39 patients with AIH-1 and 22 controls. Patients were almost exclusively DRB1∗1301, but half of controls typed DRB1∗1302. HLA-DQ haplotypes were varied. Oligotyping of DRB3 locus of all patients and also within the HLA-DR13 positive group showed an allele distribution comparable to controls, confirming that the stronger association lies in the DRB1 locus. On the other hand, if DRB1∗1301 is the major susceptibility factor in our sample, the only amino acid different from DRB1∗1302 in position 86, corresponding to pocket 1 in the peptide-presenting groove, may be important. We propose that peptide presentation leading to pathogenesis of AIH-1 may be quite stringent, but will also be affected by other strong genetic or environmental susceptibility factors, which would explain the various HLA molecules associated to the disease in the different populations. |
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However, in Brazil, disease susceptibility is primarily linked to DR13 and DR52. In this highly admixed population, we find different DR13-associated haplotypes, presenting a unique opportunity to discriminate relevant genes within a tightly linked genomic region. To identify the primary susceptibility locus, we sequenced DR13 alleles of 39 patients with AIH-1 and 22 controls. Patients were almost exclusively DRB1∗1301, but half of controls typed DRB1∗1302. HLA-DQ haplotypes were varied. Oligotyping of DRB3 locus of all patients and also within the HLA-DR13 positive group showed an allele distribution comparable to controls, confirming that the stronger association lies in the DRB1 locus. On the other hand, if DRB1∗1301 is the major susceptibility factor in our sample, the only amino acid different from DRB1∗1302 in position 86, corresponding to pocket 1 in the peptide-presenting groove, may be important. We propose that peptide presentation leading to pathogenesis of AIH-1 may be quite stringent, but will also be affected by other strong genetic or environmental susceptibility factors, which would explain the various HLA molecules associated to the disease in the different populations.</description><identifier>ISSN: 0198-8859</identifier><identifier>EISSN: 1879-1166</identifier><identifier>DOI: 10.1016/S0198-8859(00)00234-2</identifier><identifier>PMID: 11182227</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alleles ; Amino Acid Motifs - genetics ; autoimmune hepatitis ; Brazil ; Genetic Markers - immunology ; Genetic Predisposition to Disease - genetics ; genetic susceptibility ; Haplotypes - immunology ; Hepatitis, Autoimmune - classification ; Hepatitis, Autoimmune - etiology ; Hepatitis, Autoimmune - genetics ; Hepatitis, Autoimmune - immunology ; histocompatibility locus HLA ; Histocompatibility Testing ; HLA Antigens - genetics ; HLA genes ; HLA-DQ alpha-Chains ; HLA-DQ Antigens - genetics ; HLA-DQ beta-Chains ; HLA-DR Antigens - genetics ; HLA-DRB1 Chains ; HLA-DRB3 Chains ; Humans ; peptide presentation</subject><ispartof>Human immunology, 2001-02, Vol.62 (2), p.165-169</ispartof><rights>2001 American Society for Histocompatibility and Immunogenetics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-76743893523e94888c29c70492922b57a2101dad7507e19304c1caac91b086dd3</citedby><cites>FETCH-LOGICAL-c458t-76743893523e94888c29c70492922b57a2101dad7507e19304c1caac91b086dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0198-8859(00)00234-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11182227$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goldberg, Anna Carla</creatorcontrib><creatorcontrib>Bittencourt, Paulo L</creatorcontrib><creatorcontrib>Mougin, Bruno</creatorcontrib><creatorcontrib>Cançado, Eduardo L.R</creatorcontrib><creatorcontrib>Porta, Gilda</creatorcontrib><creatorcontrib>Carrilho, Flair</creatorcontrib><creatorcontrib>Kalil, Jorge</creatorcontrib><title>Analysis of HLA haplotypes in autoimmune hepatitis type 1: identifying the major susceptibility locus</title><title>Human immunology</title><addtitle>Hum Immunol</addtitle><description>Susceptibility to autoimmune hepatitis type I (AIH-1) has been associated with HLA-DR3, DR52, and DR4 antigens in Caucasian and Oriental patients. However, in Brazil, disease susceptibility is primarily linked to DR13 and DR52. In this highly admixed population, we find different DR13-associated haplotypes, presenting a unique opportunity to discriminate relevant genes within a tightly linked genomic region. To identify the primary susceptibility locus, we sequenced DR13 alleles of 39 patients with AIH-1 and 22 controls. Patients were almost exclusively DRB1∗1301, but half of controls typed DRB1∗1302. HLA-DQ haplotypes were varied. Oligotyping of DRB3 locus of all patients and also within the HLA-DR13 positive group showed an allele distribution comparable to controls, confirming that the stronger association lies in the DRB1 locus. On the other hand, if DRB1∗1301 is the major susceptibility factor in our sample, the only amino acid different from DRB1∗1302 in position 86, corresponding to pocket 1 in the peptide-presenting groove, may be important. We propose that peptide presentation leading to pathogenesis of AIH-1 may be quite stringent, but will also be affected by other strong genetic or environmental susceptibility factors, which would explain the various HLA molecules associated to the disease in the different populations.</description><subject>Alleles</subject><subject>Amino Acid Motifs - genetics</subject><subject>autoimmune hepatitis</subject><subject>Brazil</subject><subject>Genetic Markers - immunology</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>genetic susceptibility</subject><subject>Haplotypes - immunology</subject><subject>Hepatitis, Autoimmune - classification</subject><subject>Hepatitis, Autoimmune - etiology</subject><subject>Hepatitis, Autoimmune - genetics</subject><subject>Hepatitis, Autoimmune - immunology</subject><subject>histocompatibility locus HLA</subject><subject>Histocompatibility Testing</subject><subject>HLA Antigens - genetics</subject><subject>HLA genes</subject><subject>HLA-DQ alpha-Chains</subject><subject>HLA-DQ Antigens - genetics</subject><subject>HLA-DQ beta-Chains</subject><subject>HLA-DR Antigens - genetics</subject><subject>HLA-DRB1 Chains</subject><subject>HLA-DRB3 Chains</subject><subject>Humans</subject><subject>peptide presentation</subject><issn>0198-8859</issn><issn>1879-1166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUlPwzAQhS0EgrL8BJBPCA6BsbPY5oKqik2qxAE4W64zpUZJHGIHKf-elFZw5DSH-d4s7xFyyuCKASuuX4ApmUiZqwuASwCeZgnfIRMmhUoYK4pdMvlFDshhCB8AIEBk--SAMSY552JCcNqYagguUL-kj_MpXZm28nFoMVDXUNNH7-q6b5CusDXRxZFcdym7oa7EJrrl4Jp3GldIa_PhOxr6YLGNbuEqFwdaeduHY7K3NFXAk209Im_3d6-zx2T-_PA0m84Tm-UyJqIQWSpVmvMUVSaltFxZAZniivNFLgwfXy9NKXIQyFQKmWXWGKvYAmRRlukROd_MbTv_2WOIunbjNVVlGvR90AKKlIPM_gWZkAUXKR_BfAPazofQ4VK3natNN2gGeh2E_glCr13WAPonCL3WnW0X9Isayz_V1vkRuN0AOPrx5bDTwTpsLJauQxt16d0_K74BwMKXjA</recordid><startdate>20010201</startdate><enddate>20010201</enddate><creator>Goldberg, Anna Carla</creator><creator>Bittencourt, Paulo L</creator><creator>Mougin, Bruno</creator><creator>Cançado, Eduardo L.R</creator><creator>Porta, Gilda</creator><creator>Carrilho, Flair</creator><creator>Kalil, Jorge</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20010201</creationdate><title>Analysis of HLA haplotypes in autoimmune hepatitis type 1: identifying the major susceptibility locus</title><author>Goldberg, Anna Carla ; Bittencourt, Paulo L ; Mougin, Bruno ; Cançado, Eduardo L.R ; Porta, Gilda ; Carrilho, Flair ; Kalil, Jorge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-76743893523e94888c29c70492922b57a2101dad7507e19304c1caac91b086dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Alleles</topic><topic>Amino Acid Motifs - genetics</topic><topic>autoimmune hepatitis</topic><topic>Brazil</topic><topic>Genetic Markers - immunology</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>genetic susceptibility</topic><topic>Haplotypes - immunology</topic><topic>Hepatitis, Autoimmune - classification</topic><topic>Hepatitis, Autoimmune - etiology</topic><topic>Hepatitis, Autoimmune - genetics</topic><topic>Hepatitis, Autoimmune - immunology</topic><topic>histocompatibility locus HLA</topic><topic>Histocompatibility Testing</topic><topic>HLA Antigens - genetics</topic><topic>HLA genes</topic><topic>HLA-DQ alpha-Chains</topic><topic>HLA-DQ Antigens - genetics</topic><topic>HLA-DQ beta-Chains</topic><topic>HLA-DR Antigens - genetics</topic><topic>HLA-DRB1 Chains</topic><topic>HLA-DRB3 Chains</topic><topic>Humans</topic><topic>peptide presentation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goldberg, Anna Carla</creatorcontrib><creatorcontrib>Bittencourt, Paulo L</creatorcontrib><creatorcontrib>Mougin, Bruno</creatorcontrib><creatorcontrib>Cançado, Eduardo L.R</creatorcontrib><creatorcontrib>Porta, Gilda</creatorcontrib><creatorcontrib>Carrilho, Flair</creatorcontrib><creatorcontrib>Kalil, Jorge</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goldberg, Anna Carla</au><au>Bittencourt, Paulo L</au><au>Mougin, Bruno</au><au>Cançado, Eduardo L.R</au><au>Porta, Gilda</au><au>Carrilho, Flair</au><au>Kalil, Jorge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of HLA haplotypes in autoimmune hepatitis type 1: identifying the major susceptibility locus</atitle><jtitle>Human immunology</jtitle><addtitle>Hum Immunol</addtitle><date>2001-02-01</date><risdate>2001</risdate><volume>62</volume><issue>2</issue><spage>165</spage><epage>169</epage><pages>165-169</pages><issn>0198-8859</issn><eissn>1879-1166</eissn><abstract>Susceptibility to autoimmune hepatitis type I (AIH-1) has been associated with HLA-DR3, DR52, and DR4 antigens in Caucasian and Oriental patients. However, in Brazil, disease susceptibility is primarily linked to DR13 and DR52. In this highly admixed population, we find different DR13-associated haplotypes, presenting a unique opportunity to discriminate relevant genes within a tightly linked genomic region. To identify the primary susceptibility locus, we sequenced DR13 alleles of 39 patients with AIH-1 and 22 controls. Patients were almost exclusively DRB1∗1301, but half of controls typed DRB1∗1302. HLA-DQ haplotypes were varied. Oligotyping of DRB3 locus of all patients and also within the HLA-DR13 positive group showed an allele distribution comparable to controls, confirming that the stronger association lies in the DRB1 locus. On the other hand, if DRB1∗1301 is the major susceptibility factor in our sample, the only amino acid different from DRB1∗1302 in position 86, corresponding to pocket 1 in the peptide-presenting groove, may be important. We propose that peptide presentation leading to pathogenesis of AIH-1 may be quite stringent, but will also be affected by other strong genetic or environmental susceptibility factors, which would explain the various HLA molecules associated to the disease in the different populations.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11182227</pmid><doi>10.1016/S0198-8859(00)00234-2</doi><tpages>5</tpages></addata></record> |
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subjects | Alleles Amino Acid Motifs - genetics autoimmune hepatitis Brazil Genetic Markers - immunology Genetic Predisposition to Disease - genetics genetic susceptibility Haplotypes - immunology Hepatitis, Autoimmune - classification Hepatitis, Autoimmune - etiology Hepatitis, Autoimmune - genetics Hepatitis, Autoimmune - immunology histocompatibility locus HLA Histocompatibility Testing HLA Antigens - genetics HLA genes HLA-DQ alpha-Chains HLA-DQ Antigens - genetics HLA-DQ beta-Chains HLA-DR Antigens - genetics HLA-DRB1 Chains HLA-DRB3 Chains Humans peptide presentation |
title | Analysis of HLA haplotypes in autoimmune hepatitis type 1: identifying the major susceptibility locus |
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