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HLA associations in inflammatory arthritis: emerging mechanisms and clinical implications
Our understanding of the mechanisms underlying HLA associations with inflammatory arthritis continues to evolve. Disease associations have been refined, and interactions of HLA genotype with other genes and environmental risk factors in determining disease risk have been identified. This Review prov...
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Published in: | Nature reviews. Rheumatology 2019-06, Vol.15 (6), p.364-381 |
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description | Our understanding of the mechanisms underlying HLA associations with inflammatory arthritis continues to evolve. Disease associations have been refined, and interactions of HLA genotype with other genes and environmental risk factors in determining disease risk have been identified. This Review provides basic information on the genetics and molecular function of HLA molecules, as well as general features of HLA associations with disease. Evidence is discussed regarding the various peptide-dependent and peptide-independent mechanisms by which HLA alleles might contribute to the pathogenesis of three types of inflammatory arthritis: rheumatoid arthritis, spondyloarthritis and systemic juvenile idiopathic arthritis. Also discussed are HLA allelic associations that shed light on the genetic heterogeneity of inflammatory arthritides and on the relationships between adult and paediatric forms of arthritis. Clinical implications range from improved diagnosis and outcome prediction to the possibility of using HLA associations in developing personalized strategies for the treatment and prevention of these diseases.
The HLA region is strongly associated with many rheumatic diseases, including inflammatory arthritis. In this Review, potential mechanisms underpinning these associations are discussed, as are the clinical implications of HLA associations for the diagnosis and treatment of these diseases.
Key points
The HLA gene complex is one of the best-studied regions of the human genome, and technical advances continue to deepen our understanding of its associations with inflammatory arthritis.
HLA genotypes corroborate distinct clinical and immunological subtypes between patients with the same clinical diagnosis or within the juvenile idiopathic arthritis umbrella.
HLA associations are helping to clarify mechanistic overlap between paediatric and adult forms of arthritis.
In some rheumatic conditions, potential mechanisms to explain HLA associations are emerging: shared epitope (SE)-dependent neoantigen presentation in anti-citrullinated protein antibody (ACPA)-positive rheumatoid arthritis and HLA-B27 open conformations stimulating innate immune receptors in spondyloarthritis, among others.
HLA associations can provide adjuncts to diagnosis and prognosis of rheumatic conditions, and novel therapeutic and preventive approaches might develop from further mechanistic studies of these associations. |
doi_str_mv | 10.1038/s41584-019-0219-5 |
format | article |
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The HLA region is strongly associated with many rheumatic diseases, including inflammatory arthritis. In this Review, potential mechanisms underpinning these associations are discussed, as are the clinical implications of HLA associations for the diagnosis and treatment of these diseases.
Key points
The HLA gene complex is one of the best-studied regions of the human genome, and technical advances continue to deepen our understanding of its associations with inflammatory arthritis.
HLA genotypes corroborate distinct clinical and immunological subtypes between patients with the same clinical diagnosis or within the juvenile idiopathic arthritis umbrella.
HLA associations are helping to clarify mechanistic overlap between paediatric and adult forms of arthritis.
In some rheumatic conditions, potential mechanisms to explain HLA associations are emerging: shared epitope (SE)-dependent neoantigen presentation in anti-citrullinated protein antibody (ACPA)-positive rheumatoid arthritis and HLA-B27 open conformations stimulating innate immune receptors in spondyloarthritis, among others.
HLA associations can provide adjuncts to diagnosis and prognosis of rheumatic conditions, and novel therapeutic and preventive approaches might develop from further mechanistic studies of these associations.</description><identifier>ISSN: 1759-4790</identifier><identifier>EISSN: 1759-4804</identifier><identifier>DOI: 10.1038/s41584-019-0219-5</identifier><identifier>PMID: 31092910</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/250/21 ; 692/4023/1670/2766 ; 692/4023/1670/427/1304 ; 692/4023/1670/498 ; 692/420/2780 ; Antigen presentation ; Arthritis ; Arthritis - etiology ; Arthritis - genetics ; Care and treatment ; Citrulline ; Development and progression ; Diagnosis ; Gene expression ; Genetic aspects ; Genomes ; Genotypes ; Health aspects ; Histocompatibility antigen HLA ; Histocompatibility antigens ; HLA Antigens - genetics ; HLA Antigens - physiology ; HLA histocompatibility antigens ; Humans ; Inflammation ; Inflammation - etiology ; Inflammation - genetics ; Inflammatory diseases ; Medicine ; Medicine & Public Health ; Peptides ; Review Article ; Rheumatic diseases ; Rheumatoid arthritis ; Rheumatology ; Risk factors</subject><ispartof>Nature reviews. Rheumatology, 2019-06, Vol.15 (6), p.364-381</ispartof><rights>Springer Nature Limited 2019</rights><rights>COPYRIGHT 2019 Nature Publishing Group</rights><rights>Springer Nature Limited 2019.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c579t-4c4f2e90a61581ac3ef498be9183a25d9793b617b6c09d8244974a3cf9ca8bdb3</citedby><cites>FETCH-LOGICAL-c579t-4c4f2e90a61581ac3ef498be9183a25d9793b617b6c09d8244974a3cf9ca8bdb3</cites><orcidid>0000-0002-4132-0751 ; 0000-0003-2577-139X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31092910$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Busch, Robert</creatorcontrib><creatorcontrib>Kollnberger, Simon</creatorcontrib><creatorcontrib>Mellins, Elizabeth D.</creatorcontrib><title>HLA associations in inflammatory arthritis: emerging mechanisms and clinical implications</title><title>Nature reviews. Rheumatology</title><addtitle>Nat Rev Rheumatol</addtitle><addtitle>Nat Rev Rheumatol</addtitle><description>Our understanding of the mechanisms underlying HLA associations with inflammatory arthritis continues to evolve. Disease associations have been refined, and interactions of HLA genotype with other genes and environmental risk factors in determining disease risk have been identified. This Review provides basic information on the genetics and molecular function of HLA molecules, as well as general features of HLA associations with disease. Evidence is discussed regarding the various peptide-dependent and peptide-independent mechanisms by which HLA alleles might contribute to the pathogenesis of three types of inflammatory arthritis: rheumatoid arthritis, spondyloarthritis and systemic juvenile idiopathic arthritis. Also discussed are HLA allelic associations that shed light on the genetic heterogeneity of inflammatory arthritides and on the relationships between adult and paediatric forms of arthritis. Clinical implications range from improved diagnosis and outcome prediction to the possibility of using HLA associations in developing personalized strategies for the treatment and prevention of these diseases.
The HLA region is strongly associated with many rheumatic diseases, including inflammatory arthritis. In this Review, potential mechanisms underpinning these associations are discussed, as are the clinical implications of HLA associations for the diagnosis and treatment of these diseases.
Key points
The HLA gene complex is one of the best-studied regions of the human genome, and technical advances continue to deepen our understanding of its associations with inflammatory arthritis.
HLA genotypes corroborate distinct clinical and immunological subtypes between patients with the same clinical diagnosis or within the juvenile idiopathic arthritis umbrella.
HLA associations are helping to clarify mechanistic overlap between paediatric and adult forms of arthritis.
In some rheumatic conditions, potential mechanisms to explain HLA associations are emerging: shared epitope (SE)-dependent neoantigen presentation in anti-citrullinated protein antibody (ACPA)-positive rheumatoid arthritis and HLA-B27 open conformations stimulating innate immune receptors in spondyloarthritis, among others.
HLA associations can provide adjuncts to diagnosis and prognosis of rheumatic conditions, and novel therapeutic and preventive approaches might develop from further mechanistic studies of these associations.</description><subject>631/250/21</subject><subject>692/4023/1670/2766</subject><subject>692/4023/1670/427/1304</subject><subject>692/4023/1670/498</subject><subject>692/420/2780</subject><subject>Antigen presentation</subject><subject>Arthritis</subject><subject>Arthritis - etiology</subject><subject>Arthritis - genetics</subject><subject>Care and treatment</subject><subject>Citrulline</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Genotypes</subject><subject>Health aspects</subject><subject>Histocompatibility antigen HLA</subject><subject>Histocompatibility antigens</subject><subject>HLA Antigens - genetics</subject><subject>HLA Antigens - physiology</subject><subject>HLA histocompatibility antigens</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Inflammation - etiology</subject><subject>Inflammation - genetics</subject><subject>Inflammatory diseases</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Peptides</subject><subject>Review Article</subject><subject>Rheumatic diseases</subject><subject>Rheumatoid arthritis</subject><subject>Rheumatology</subject><subject>Risk factors</subject><issn>1759-4790</issn><issn>1759-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kc1rFDEYxoMotlb_AC8yIIiXafM1mcTbUtQKC17qwVN4J5PZTcnHmswc-t83222tlZaEJCS_5yHv-yD0nuBTgpk8K5x0kreYqBbTunQv0DHpO9VyifnL-3Ov8BF6U8oVxoILqV6jI0awoorgY_T7Yr1qoJRkHMwuxdK4WOfkIQSYU75uIM_b7GZXvjQ22LxxcdMEa7YQXQmlgTg2xrvoDPjGhZ2vh1ujt-jVBL7Yd3f7Cfr17evl-UW7_vn9x_lq3ZquV3PLDZ-oVRhErYWAYXbiSg5WEcmAdqPqFRsE6QdhsBol5Vz1HJiZlAE5jAM7QZ8Pvruc_iy2zDq4Yqz3EG1aiqaUUcwE7XhFP_6HXqUlx_q7SlFVG8J4_0BtwFtde5HmDGZvqledFIISIUilTp-g6hhtcCZFO7l6_0jw6R_B1oKftyX55bZZj0FyAE1OpWQ76V12AfK1Jljvc9eH3HXNXe9z113VfLirbBmCHf8q7oOuAD0ApT7Fjc0PpT_vegO2YbXf</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>Busch, Robert</creator><creator>Kollnberger, Simon</creator><creator>Mellins, Elizabeth D.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4132-0751</orcidid><orcidid>https://orcid.org/0000-0003-2577-139X</orcidid></search><sort><creationdate>20190601</creationdate><title>HLA associations in inflammatory arthritis: emerging mechanisms and clinical implications</title><author>Busch, Robert ; Kollnberger, Simon ; Mellins, Elizabeth D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c579t-4c4f2e90a61581ac3ef498be9183a25d9793b617b6c09d8244974a3cf9ca8bdb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>631/250/21</topic><topic>692/4023/1670/2766</topic><topic>692/4023/1670/427/1304</topic><topic>692/4023/1670/498</topic><topic>692/420/2780</topic><topic>Antigen presentation</topic><topic>Arthritis</topic><topic>Arthritis - etiology</topic><topic>Arthritis - genetics</topic><topic>Care and treatment</topic><topic>Citrulline</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Genomes</topic><topic>Genotypes</topic><topic>Health aspects</topic><topic>Histocompatibility antigen HLA</topic><topic>Histocompatibility antigens</topic><topic>HLA Antigens - genetics</topic><topic>HLA Antigens - physiology</topic><topic>HLA histocompatibility antigens</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Inflammation - etiology</topic><topic>Inflammation - genetics</topic><topic>Inflammatory diseases</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Peptides</topic><topic>Review Article</topic><topic>Rheumatic diseases</topic><topic>Rheumatoid arthritis</topic><topic>Rheumatology</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Busch, Robert</creatorcontrib><creatorcontrib>Kollnberger, Simon</creatorcontrib><creatorcontrib>Mellins, Elizabeth D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Health and Medical Complete</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Nature reviews. Rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Busch, Robert</au><au>Kollnberger, Simon</au><au>Mellins, Elizabeth D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HLA associations in inflammatory arthritis: emerging mechanisms and clinical implications</atitle><jtitle>Nature reviews. Rheumatology</jtitle><stitle>Nat Rev Rheumatol</stitle><addtitle>Nat Rev Rheumatol</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>15</volume><issue>6</issue><spage>364</spage><epage>381</epage><pages>364-381</pages><issn>1759-4790</issn><eissn>1759-4804</eissn><abstract>Our understanding of the mechanisms underlying HLA associations with inflammatory arthritis continues to evolve. Disease associations have been refined, and interactions of HLA genotype with other genes and environmental risk factors in determining disease risk have been identified. This Review provides basic information on the genetics and molecular function of HLA molecules, as well as general features of HLA associations with disease. Evidence is discussed regarding the various peptide-dependent and peptide-independent mechanisms by which HLA alleles might contribute to the pathogenesis of three types of inflammatory arthritis: rheumatoid arthritis, spondyloarthritis and systemic juvenile idiopathic arthritis. Also discussed are HLA allelic associations that shed light on the genetic heterogeneity of inflammatory arthritides and on the relationships between adult and paediatric forms of arthritis. Clinical implications range from improved diagnosis and outcome prediction to the possibility of using HLA associations in developing personalized strategies for the treatment and prevention of these diseases.
The HLA region is strongly associated with many rheumatic diseases, including inflammatory arthritis. In this Review, potential mechanisms underpinning these associations are discussed, as are the clinical implications of HLA associations for the diagnosis and treatment of these diseases.
Key points
The HLA gene complex is one of the best-studied regions of the human genome, and technical advances continue to deepen our understanding of its associations with inflammatory arthritis.
HLA genotypes corroborate distinct clinical and immunological subtypes between patients with the same clinical diagnosis or within the juvenile idiopathic arthritis umbrella.
HLA associations are helping to clarify mechanistic overlap between paediatric and adult forms of arthritis.
In some rheumatic conditions, potential mechanisms to explain HLA associations are emerging: shared epitope (SE)-dependent neoantigen presentation in anti-citrullinated protein antibody (ACPA)-positive rheumatoid arthritis and HLA-B27 open conformations stimulating innate immune receptors in spondyloarthritis, among others.
HLA associations can provide adjuncts to diagnosis and prognosis of rheumatic conditions, and novel therapeutic and preventive approaches might develop from further mechanistic studies of these associations.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31092910</pmid><doi>10.1038/s41584-019-0219-5</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0002-4132-0751</orcidid><orcidid>https://orcid.org/0000-0003-2577-139X</orcidid><oa>free_for_read</oa></addata></record> |
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title | HLA associations in inflammatory arthritis: emerging mechanisms and clinical implications |
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