A Simplified PCR-SSP Method for HLA-A2 Subtype in a Population of Wuhan, China
HLA-A2 is the most frequent HLA-A allele in all ethnic populations, and an important restriction element for peptide presentation to T cells in infectious disease and cancer. However, the HLA-A2 supertype consisting of up to 75 subtypes, mutation studies and analyses using cytotoxic T lymphocytes su...
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description | HLA-A2 is the most frequent HLA-A allele in all ethnic populations, and an important restriction element for peptide presentation to T cells in infectious disease and cancer. However, the HLA-A2 supertype consisting of up to 75 subtypes, mutation studies and analyses using cytotoxic T lymphocytes suggest the functional relevance of subtype-specific differences in HLA-A2 molecules for peptide binding and T-cell recognition. Therefore, it is necessary for T-cell response study to discriminate the HLA-A2 subtypes and to understand the profile of HLA-A2 allellc distribution in a given population. In this study, we developed a simple, robust approach based on the nested polymerase chain reaction using sequence-specific primers (PCR-SSP) to discriminate 17 HLA-A2 subtypes which cover the most HLA-A2 alleles (〉 99% allele frequency) reported in Chinese, using 15 combinations of 19 allelic specific primers. In the first round of PCR, 3 combinations of 5 primers were used to determine whether the tested sample was HLA-A2 positive, meanwhile the subtypes of HLA-A*0209 and HLA-A*0215N were determined for the variant position of these two subtypes is in exon 4 instead of exon 2, 3. Samples of HLA-A2 positive were subtyped in the second round of PCR, using PCR products of the first round as templates. This strategy was applied to test the samples of 78 random HLA-A2 positive individuals for their HLA-A2 subtypes. Those samples were screened for HLA-A2 positive by the first round PCR-SSP from 154 healthy blood donors in Wuhan, China. The subtyping results were verified by using flow cytometric analysis (FCM) with HLA-A2 specific monoclonal antibody BB7.2 and DNA sequencing. The typing results of the samples show 50.7% random individuals in the population carry HLA-A2, HLA-A*0201 ranks the first (allele frequency = 15.5%), followed by A*0207 (5.8%), A*0206 (4.7%), A*0203 (2.6%), A*0210 (0.7%), and these 5 alleles account for 99.0% HLA-A2 subtypes of allele frequency. Our study indicates that the developed typing method is simple and reliable for HLA-A2 subtyping in Chinese, and the profile of allelic distribution of HLA-A2 subtypes is revealed in the population of Wuhan, China. |
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However, the HLA-A2 supertype consisting of up to 75 subtypes, mutation studies and analyses using cytotoxic T lymphocytes suggest the functional relevance of subtype-specific differences in HLA-A2 molecules for peptide binding and T-cell recognition. Therefore, it is necessary for T-cell response study to discriminate the HLA-A2 subtypes and to understand the profile of HLA-A2 allellc distribution in a given population. In this study, we developed a simple, robust approach based on the nested polymerase chain reaction using sequence-specific primers (PCR-SSP) to discriminate 17 HLA-A2 subtypes which cover the most HLA-A2 alleles (〉 99% allele frequency) reported in Chinese, using 15 combinations of 19 allelic specific primers. In the first round of PCR, 3 combinations of 5 primers were used to determine whether the tested sample was HLA-A2 positive, meanwhile the subtypes of HLA-A*0209 and HLA-A*0215N were determined for the variant position of these two subtypes is in exon 4 instead of exon 2, 3. Samples of HLA-A2 positive were subtyped in the second round of PCR, using PCR products of the first round as templates. This strategy was applied to test the samples of 78 random HLA-A2 positive individuals for their HLA-A2 subtypes. Those samples were screened for HLA-A2 positive by the first round PCR-SSP from 154 healthy blood donors in Wuhan, China. The subtyping results were verified by using flow cytometric analysis (FCM) with HLA-A2 specific monoclonal antibody BB7.2 and DNA sequencing. The typing results of the samples show 50.7% random individuals in the population carry HLA-A2, HLA-A*0201 ranks the first (allele frequency = 15.5%), followed by A*0207 (5.8%), A*0206 (4.7%), A*0203 (2.6%), A*0210 (0.7%), and these 5 alleles account for 99.0% HLA-A2 subtypes of allele frequency. Our study indicates that the developed typing method is simple and reliable for HLA-A2 subtyping in Chinese, and the profile of allelic distribution of HLA-A2 subtypes is revealed in the population of Wuhan, China.</description><identifier>ISSN: 1672-7681</identifier><identifier>EISSN: 2042-0226</identifier><identifier>PMID: 17257499</identifier><language>eng</language><publisher>China: Department of Immunology,Tongji Medical College,Huazhong Universityof Science & Technology,Wuhan,China</publisher><subject>China ; HLA-A2 Antigen - classification ; HLA-A2 Antigen - genetics ; Humans ; Polymerase Chain Reaction ; 聚合酶链反应</subject><ispartof>Cellular & molecular immunology, 2006-12, Vol.3 (6), p.453-458</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/87787X/87787X.jpg</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17257499$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liang, Bing</creatorcontrib><creatorcontrib>Zhu, Lijun</creatorcontrib><creatorcontrib>Liang, Zhihui</creatorcontrib><creatorcontrib>Weng, Xiufang</creatorcontrib><creatorcontrib>Lu, Xiaoling</creatorcontrib><creatorcontrib>Zhang, Cai'e</creatorcontrib><creatorcontrib>Li, Hui</creatorcontrib><creatorcontrib>Wu, Xiongwen</creatorcontrib><title>A Simplified PCR-SSP Method for HLA-A2 Subtype in a Population of Wuhan, China</title><title>Cellular & molecular immunology</title><addtitle>Cellular & Molecular Immunology</addtitle><description>HLA-A2 is the most frequent HLA-A allele in all ethnic populations, and an important restriction element for peptide presentation to T cells in infectious disease and cancer. However, the HLA-A2 supertype consisting of up to 75 subtypes, mutation studies and analyses using cytotoxic T lymphocytes suggest the functional relevance of subtype-specific differences in HLA-A2 molecules for peptide binding and T-cell recognition. Therefore, it is necessary for T-cell response study to discriminate the HLA-A2 subtypes and to understand the profile of HLA-A2 allellc distribution in a given population. In this study, we developed a simple, robust approach based on the nested polymerase chain reaction using sequence-specific primers (PCR-SSP) to discriminate 17 HLA-A2 subtypes which cover the most HLA-A2 alleles (〉 99% allele frequency) reported in Chinese, using 15 combinations of 19 allelic specific primers. In the first round of PCR, 3 combinations of 5 primers were used to determine whether the tested sample was HLA-A2 positive, meanwhile the subtypes of HLA-A*0209 and HLA-A*0215N were determined for the variant position of these two subtypes is in exon 4 instead of exon 2, 3. Samples of HLA-A2 positive were subtyped in the second round of PCR, using PCR products of the first round as templates. This strategy was applied to test the samples of 78 random HLA-A2 positive individuals for their HLA-A2 subtypes. Those samples were screened for HLA-A2 positive by the first round PCR-SSP from 154 healthy blood donors in Wuhan, China. The subtyping results were verified by using flow cytometric analysis (FCM) with HLA-A2 specific monoclonal antibody BB7.2 and DNA sequencing. The typing results of the samples show 50.7% random individuals in the population carry HLA-A2, HLA-A*0201 ranks the first (allele frequency = 15.5%), followed by A*0207 (5.8%), A*0206 (4.7%), A*0203 (2.6%), A*0210 (0.7%), and these 5 alleles account for 99.0% HLA-A2 subtypes of allele frequency. Our study indicates that the developed typing method is simple and reliable for HLA-A2 subtyping in Chinese, and the profile of allelic distribution of HLA-A2 subtypes is revealed in the population of Wuhan, China.</description><subject>China</subject><subject>HLA-A2 Antigen - classification</subject><subject>HLA-A2 Antigen - genetics</subject><subject>Humans</subject><subject>Polymerase Chain Reaction</subject><subject>聚合酶链反应</subject><issn>1672-7681</issn><issn>2042-0226</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo10E9LwzAYBvAgipvTryDBgwexkKRpkh7LUCdMHVbxGNI2WTPbpOsfdPv0FjZ5D8_lx_PAewKmBFESIELYKZhixknAmcATcNF1G4QiQTk9BxPMScRpHE_BawJTWzeVNVYXcDV_D9J0BV90X_oCGt_CxTIJEgLTIet3jYbWQQVXvhkq1VvvoDfwayiVu4fz0jp1Cc6Mqjp9dcwZ-Hx8-JgvguXb0_M8WQY54bgPMI0iSiLEdIiMjnVe8ExkGcrDGAtGixhrRaNcCMUjFppIFAJlnFNa5DFhSIczcHfo_VHOKLeWGz-0blyU-3W9-93vpSYIsfEQH_HtATet3w6662Vtu1xXlXLaD51kIsQoDvEIr49wyGpdyKa1tWp38v9dI7g5gLz0br2143Cm8m9jKy1JyDiLCQr_AA-pbxw</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>Liang, Bing</creator><creator>Zhu, Lijun</creator><creator>Liang, Zhihui</creator><creator>Weng, Xiufang</creator><creator>Lu, Xiaoling</creator><creator>Zhang, Cai'e</creator><creator>Li, Hui</creator><creator>Wu, Xiongwen</creator><general>Department of Immunology,Tongji Medical College,Huazhong Universityof Science & Technology,Wuhan,China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>WU4</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20061201</creationdate><title>A Simplified PCR-SSP Method for HLA-A2 Subtype in a Population of Wuhan, China</title><author>Liang, Bing ; Zhu, Lijun ; Liang, Zhihui ; Weng, Xiufang ; Lu, Xiaoling ; Zhang, Cai'e ; Li, Hui ; Wu, Xiongwen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c271t-145542506e30fe9ecd7b8bb0c391864d91ea45c88a7563f58d80b7744dc9260e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>China</topic><topic>HLA-A2 Antigen - classification</topic><topic>HLA-A2 Antigen - genetics</topic><topic>Humans</topic><topic>Polymerase Chain Reaction</topic><topic>聚合酶链反应</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liang, Bing</creatorcontrib><creatorcontrib>Zhu, Lijun</creatorcontrib><creatorcontrib>Liang, Zhihui</creatorcontrib><creatorcontrib>Weng, Xiufang</creatorcontrib><creatorcontrib>Lu, Xiaoling</creatorcontrib><creatorcontrib>Zhang, Cai'e</creatorcontrib><creatorcontrib>Li, Hui</creatorcontrib><creatorcontrib>Wu, Xiongwen</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-自然科学</collection><collection>中文科技期刊数据库-自然科学-生物科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Cellular & molecular immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liang, Bing</au><au>Zhu, Lijun</au><au>Liang, Zhihui</au><au>Weng, Xiufang</au><au>Lu, Xiaoling</au><au>Zhang, Cai'e</au><au>Li, Hui</au><au>Wu, Xiongwen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Simplified PCR-SSP Method for HLA-A2 Subtype in a Population of Wuhan, China</atitle><jtitle>Cellular & molecular immunology</jtitle><addtitle>Cellular & Molecular Immunology</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>3</volume><issue>6</issue><spage>453</spage><epage>458</epage><pages>453-458</pages><issn>1672-7681</issn><eissn>2042-0226</eissn><abstract>HLA-A2 is the most frequent HLA-A allele in all ethnic populations, and an important restriction element for peptide presentation to T cells in infectious disease and cancer. However, the HLA-A2 supertype consisting of up to 75 subtypes, mutation studies and analyses using cytotoxic T lymphocytes suggest the functional relevance of subtype-specific differences in HLA-A2 molecules for peptide binding and T-cell recognition. Therefore, it is necessary for T-cell response study to discriminate the HLA-A2 subtypes and to understand the profile of HLA-A2 allellc distribution in a given population. In this study, we developed a simple, robust approach based on the nested polymerase chain reaction using sequence-specific primers (PCR-SSP) to discriminate 17 HLA-A2 subtypes which cover the most HLA-A2 alleles (〉 99% allele frequency) reported in Chinese, using 15 combinations of 19 allelic specific primers. In the first round of PCR, 3 combinations of 5 primers were used to determine whether the tested sample was HLA-A2 positive, meanwhile the subtypes of HLA-A*0209 and HLA-A*0215N were determined for the variant position of these two subtypes is in exon 4 instead of exon 2, 3. Samples of HLA-A2 positive were subtyped in the second round of PCR, using PCR products of the first round as templates. This strategy was applied to test the samples of 78 random HLA-A2 positive individuals for their HLA-A2 subtypes. Those samples were screened for HLA-A2 positive by the first round PCR-SSP from 154 healthy blood donors in Wuhan, China. The subtyping results were verified by using flow cytometric analysis (FCM) with HLA-A2 specific monoclonal antibody BB7.2 and DNA sequencing. The typing results of the samples show 50.7% random individuals in the population carry HLA-A2, HLA-A*0201 ranks the first (allele frequency = 15.5%), followed by A*0207 (5.8%), A*0206 (4.7%), A*0203 (2.6%), A*0210 (0.7%), and these 5 alleles account for 99.0% HLA-A2 subtypes of allele frequency. Our study indicates that the developed typing method is simple and reliable for HLA-A2 subtyping in Chinese, and the profile of allelic distribution of HLA-A2 subtypes is revealed in the population of Wuhan, China.</abstract><cop>China</cop><pub>Department of Immunology,Tongji Medical College,Huazhong Universityof Science & Technology,Wuhan,China</pub><pmid>17257499</pmid><tpages>6</tpages></addata></record> |
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subjects | China HLA-A2 Antigen - classification HLA-A2 Antigen - genetics Humans Polymerase Chain Reaction 聚合酶链反应 |
title | A Simplified PCR-SSP Method for HLA-A2 Subtype in a Population of Wuhan, China |
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