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High-Throughput Analysis of the T Cell Receptor Beta Chain Repertoire in PBMCs from Chronic Hepatitis B Patients with HBeAg Seroconversion
T lymphocytes are the most important immune cells that affect both the development and treatment of hepatitis B. We used high-throughput sequencing to determine the diversity in the V and J regions of the TCRβ chain in 4 chronic hepatitis B patients before and after HBeAg seroconversion. Here, we de...
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Published in: | The Canadian journal of infectious diseases & medical microbiology 2016-01, Vol.2016 (2016), p.1-7 |
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container_title | The Canadian journal of infectious diseases & medical microbiology |
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description | T lymphocytes are the most important immune cells that affect both the development and treatment of hepatitis B. We used high-throughput sequencing to determine the diversity in the V and J regions of the TCRβ chain in 4 chronic hepatitis B patients before and after HBeAg seroconversion. Here, we demonstrate that the 4 patients expressed Vβ12-4 at the highest frequencies of 10.6%, 9.2%, 17.5%, and 7.5%, and Vβ28 was the second most common, with frequencies of 7.8%, 6.7%, 5.3%, and 10.9%, respectively. No significant changes were observed following seroconversion. With regard to the Jβ gene, Jβ2-1 was the most commonly expressed in the 4 patients at frequencies of 5.8%, 6.5%, 11.3%, and 7.3%, respectively. Analysis of the V-J region genes revealed several differences, including significant increases in the expression levels of V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 and a decrease in that of V19-01-J2-3. These results illustrate the presence of biased TCRVβ and Jβ gene expression in the chronic hepatitis B patients. TRBVβ12-4, Vβ28, Jβ2-1, V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 may be associated with the development and treatment of CHB. |
doi_str_mv | 10.1155/2016/8594107 |
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We used high-throughput sequencing to determine the diversity in the V and J regions of the TCRβ chain in 4 chronic hepatitis B patients before and after HBeAg seroconversion. Here, we demonstrate that the 4 patients expressed Vβ12-4 at the highest frequencies of 10.6%, 9.2%, 17.5%, and 7.5%, and Vβ28 was the second most common, with frequencies of 7.8%, 6.7%, 5.3%, and 10.9%, respectively. No significant changes were observed following seroconversion. With regard to the Jβ gene, Jβ2-1 was the most commonly expressed in the 4 patients at frequencies of 5.8%, 6.5%, 11.3%, and 7.3%, respectively. Analysis of the V-J region genes revealed several differences, including significant increases in the expression levels of V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 and a decrease in that of V19-01-J2-3. These results illustrate the presence of biased TCRVβ and Jβ gene expression in the chronic hepatitis B patients. TRBVβ12-4, Vβ28, Jβ2-1, V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 may be associated with the development and treatment of CHB.</description><identifier>ISSN: 1712-9532</identifier><identifier>EISSN: 1918-1493</identifier><identifier>DOI: 10.1155/2016/8594107</identifier><identifier>PMID: 27818694</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Antigens ; Chains ; Crystal structure ; Disease ; Gene expression ; Genes ; Genetic aspects ; Health aspects ; Hepatitis ; Hepatitis associated antigen ; Hepatitis B ; Hepatitis B e antigen ; Hospitals ; Immune system ; Infections ; Infectious diseases ; Liver cancer ; Lymphocytes ; Lymphocytes T ; Next-generation sequencing ; Pathogenesis ; Patients ; Seroconversion ; Studies ; T cell receptors ; T cells</subject><ispartof>The Canadian journal of infectious diseases & medical microbiology, 2016-01, Vol.2016 (2016), p.1-7</ispartof><rights>Copyright © 2016 Yachao Qu et al.</rights><rights>COPYRIGHT 2016 John Wiley & Sons, Inc.</rights><rights>Copyright © 2016 Yachao Qu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2016 Yachao Qu et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c662t-a080d1052d31f35ded62e1f7d94e62dd7eb21d1a587d73074de705ab804797ed3</citedby><cites>FETCH-LOGICAL-c662t-a080d1052d31f35ded62e1f7d94e62dd7eb21d1a587d73074de705ab804797ed3</cites><orcidid>0000-0002-1269-9678 ; 0000-0003-4237-6404 ; 0000-0002-7491-5073 ; 0000-0002-8503-8045 ; 0000-0001-7466-5054</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1831181947/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1831181947?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27818694$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Semnani, Roshanak Tolouei</contributor><creatorcontrib>Lu, Jun</creatorcontrib><creatorcontrib>Tong, Yigang</creatorcontrib><creatorcontrib>Mi, Zhiqiang</creatorcontrib><creatorcontrib>Zhang, Zhiyi</creatorcontrib><creatorcontrib>Huang, Yinuo</creatorcontrib><creatorcontrib>Liu, Di</creatorcontrib><creatorcontrib>Huang, Yong</creatorcontrib><creatorcontrib>Qu, Yachao</creatorcontrib><creatorcontrib>An, Xiaoping</creatorcontrib><title>High-Throughput Analysis of the T Cell Receptor Beta Chain Repertoire in PBMCs from Chronic Hepatitis B Patients with HBeAg Seroconversion</title><title>The Canadian journal of infectious diseases & medical microbiology</title><addtitle>Can J Infect Dis Med Microbiol</addtitle><description>T lymphocytes are the most important immune cells that affect both the development and treatment of hepatitis B. We used high-throughput sequencing to determine the diversity in the V and J regions of the TCRβ chain in 4 chronic hepatitis B patients before and after HBeAg seroconversion. Here, we demonstrate that the 4 patients expressed Vβ12-4 at the highest frequencies of 10.6%, 9.2%, 17.5%, and 7.5%, and Vβ28 was the second most common, with frequencies of 7.8%, 6.7%, 5.3%, and 10.9%, respectively. No significant changes were observed following seroconversion. With regard to the Jβ gene, Jβ2-1 was the most commonly expressed in the 4 patients at frequencies of 5.8%, 6.5%, 11.3%, and 7.3%, respectively. Analysis of the V-J region genes revealed several differences, including significant increases in the expression levels of V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 and a decrease in that of V19-01-J2-3. These results illustrate the presence of biased TCRVβ and Jβ gene expression in the chronic hepatitis B patients. TRBVβ12-4, Vβ28, Jβ2-1, V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 may be associated with the development and treatment of CHB.</description><subject>Antigens</subject><subject>Chains</subject><subject>Crystal structure</subject><subject>Disease</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Hepatitis</subject><subject>Hepatitis associated antigen</subject><subject>Hepatitis B</subject><subject>Hepatitis B e antigen</subject><subject>Hospitals</subject><subject>Immune system</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Liver cancer</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Next-generation sequencing</subject><subject>Pathogenesis</subject><subject>Patients</subject><subject>Seroconversion</subject><subject>Studies</subject><subject>T cell receptors</subject><subject>T cells</subject><issn>1712-9532</issn><issn>1918-1493</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNks9v0zAUgCMEYmNw44wsJiEk6GY7sZ1ckNoK6KQhJhhny4tfGk9pnNnOpv0L_NW8rmNb0Q7Eh9jPX77o_ciy14weMCbEIadMHpaiKhhVT7JdVrFywooqf4p7xfikEjnfyV7EeE5pLjlTz7MdrkpWyqrYzX4v3LKdnLbBj8t2GBOZ9qa7ji4S35DUAjklc-g68gNqGJIPZAbJkHlrXI-xAULyLgDB08ns2zySJvgVXgffu5osYDDJJZTNyAnuoE-RXLnUksUMpkvyE4KvfX8JITrfv8yeNaaL8Or2vZf9-vL5dL6YHH__ejSfHk9qKXmaGFpSy6jgNmdNLixYyYE1ylYFSG6tgjPOLDOiVFblVBUWFBXmrKSFqhTYfC872nitN-d6CG5lwrX2xumbgA9LbUJydQdaWm7qvC6Zym1hDT7SSltgWSVVGEbXp41rGM9WYGvMMJhuS7p907tWL_2lFrRkhahQ8P5WEPzFCDHplYs1Vtz04MeoWZkrykvJBaL7_6DnfgzYrhuKsZJVhbqnlgYTcH3j8b_1WqqngiopMJm16-0jVD24C_0QOngEwmVh5bBv0DiMb1nfPfigBdOlNvpuTNjduA1-3IB18DEGaO4qxqheT7VeT7W-nWrE3zys8h38d4wR-LABWtdbc-X-UwfIQGPuaUYp5TT_A7x0BY0</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Lu, Jun</creator><creator>Tong, Yigang</creator><creator>Mi, Zhiqiang</creator><creator>Zhang, Zhiyi</creator><creator>Huang, Yinuo</creator><creator>Liu, Di</creator><creator>Huang, Yong</creator><creator>Qu, Yachao</creator><creator>An, Xiaoping</creator><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T7</scope><scope>7X7</scope><scope>7XB</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1269-9678</orcidid><orcidid>https://orcid.org/0000-0003-4237-6404</orcidid><orcidid>https://orcid.org/0000-0002-7491-5073</orcidid><orcidid>https://orcid.org/0000-0002-8503-8045</orcidid><orcidid>https://orcid.org/0000-0001-7466-5054</orcidid></search><sort><creationdate>20160101</creationdate><title>High-Throughput Analysis of the T Cell Receptor Beta Chain Repertoire in PBMCs from Chronic Hepatitis B Patients with HBeAg Seroconversion</title><author>Lu, Jun ; 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We used high-throughput sequencing to determine the diversity in the V and J regions of the TCRβ chain in 4 chronic hepatitis B patients before and after HBeAg seroconversion. Here, we demonstrate that the 4 patients expressed Vβ12-4 at the highest frequencies of 10.6%, 9.2%, 17.5%, and 7.5%, and Vβ28 was the second most common, with frequencies of 7.8%, 6.7%, 5.3%, and 10.9%, respectively. No significant changes were observed following seroconversion. With regard to the Jβ gene, Jβ2-1 was the most commonly expressed in the 4 patients at frequencies of 5.8%, 6.5%, 11.3%, and 7.3%, respectively. Analysis of the V-J region genes revealed several differences, including significant increases in the expression levels of V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 and a decrease in that of V19-01-J2-3. These results illustrate the presence of biased TCRVβ and Jβ gene expression in the chronic hepatitis B patients. TRBVβ12-4, Vβ28, Jβ2-1, V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 may be associated with the development and treatment of CHB.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>27818694</pmid><doi>10.1155/2016/8594107</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-1269-9678</orcidid><orcidid>https://orcid.org/0000-0003-4237-6404</orcidid><orcidid>https://orcid.org/0000-0002-7491-5073</orcidid><orcidid>https://orcid.org/0000-0002-8503-8045</orcidid><orcidid>https://orcid.org/0000-0001-7466-5054</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Chains Crystal structure Disease Gene expression Genes Genetic aspects Health aspects Hepatitis Hepatitis associated antigen Hepatitis B Hepatitis B e antigen Hospitals Immune system Infections Infectious diseases Liver cancer Lymphocytes Lymphocytes T Next-generation sequencing Pathogenesis Patients Seroconversion Studies T cell receptors T cells |
title | High-Throughput Analysis of the T Cell Receptor Beta Chain Repertoire in PBMCs from Chronic Hepatitis B Patients with HBeAg Seroconversion |
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