Longitudinal mapping of hepatitis B vaccine‐induced B‐cell linear epitopes in healthy individuals
The elimination of hepatitis B virus (HBV) infection is partially facilitated by the prophylactic HB vaccine. As the loss of seroprotection over time remains a conundrum for long‐lasting protection, a comprehensive dynamic analysis of immunogenic targets of the HB vaccine will provide novel insights...
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Veröffentlicht in: | Journal of medical virology 2022-10, Vol.94 (10), p.4993-5006 |
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description | The elimination of hepatitis B virus (HBV) infection is partially facilitated by the prophylactic HB vaccine. As the loss of seroprotection over time remains a conundrum for long‐lasting protection, a comprehensive dynamic analysis of immunogenic targets of the HB vaccine will provide novel insights into the improvement and design of potential targets. In this study, 36 healthy subjects without prior history of hepatitis B infection and negative for hepatitis B surface antibody (anti‐HBs) were enrolled. Participants were given a series of three doses of HB vaccine on a 0‐, 1‐, and 6‐month schedule and longitudinally followed up. We systematically mapped 55 overlapping 15‐mer peptides covering the small S protein of hepatitis B virus (SHBs) of vaccinees' serum samples at seven time points by performing an ELISA assay. Additionally, the frequencies and function dynamics of adaptive immune response were assessed by flow cytometry. We found that the SHBs peptide coverage presented an overall upward trend along with the vaccination progress, and the individual subpartition recognition was strongly correlated with the anti‐HBs titers. Moreover, we identified one dominant epitope (S29) located on “a determinant region” associated with effective vaccine response. Besides, significant correlations between the proportion of plasmablasts and proliferating B cells and levels of anti‐HBs were ascertained. Taken together, our data characterized the dynamics of HB vaccine‐induced neutralizing antibodies against B‐cell linear epitopes on SHBs and adaptive immune response, which will be constructive to develop the next‐generation vaccine. |
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As the loss of seroprotection over time remains a conundrum for long‐lasting protection, a comprehensive dynamic analysis of immunogenic targets of the HB vaccine will provide novel insights into the improvement and design of potential targets. In this study, 36 healthy subjects without prior history of hepatitis B infection and negative for hepatitis B surface antibody (anti‐HBs) were enrolled. Participants were given a series of three doses of HB vaccine on a 0‐, 1‐, and 6‐month schedule and longitudinally followed up. We systematically mapped 55 overlapping 15‐mer peptides covering the small S protein of hepatitis B virus (SHBs) of vaccinees' serum samples at seven time points by performing an ELISA assay. Additionally, the frequencies and function dynamics of adaptive immune response were assessed by flow cytometry. We found that the SHBs peptide coverage presented an overall upward trend along with the vaccination progress, and the individual subpartition recognition was strongly correlated with the anti‐HBs titers. Moreover, we identified one dominant epitope (S29) located on “a determinant region” associated with effective vaccine response. Besides, significant correlations between the proportion of plasmablasts and proliferating B cells and levels of anti‐HBs were ascertained. Taken together, our data characterized the dynamics of HB vaccine‐induced neutralizing antibodies against B‐cell linear epitopes on SHBs and adaptive immune response, which will be constructive to develop the next‐generation vaccine.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.27926</identifier><identifier>PMID: 35676468</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>a determinant region ; adaptive immune response ; Adaptive immunity ; Antibodies ; B‐cell linear epitopes ; Enzyme-linked immunosorbent assay ; Epitope mapping ; Flow cytometry ; Hepatitis ; Hepatitis B ; hepatitis B vaccination ; Immune response ; Immune system ; Immunogenicity ; Infections ; Lymphocytes B ; peptide mapping ; Peptides ; Vaccination ; Vaccines ; Virology ; Viruses</subject><ispartof>Journal of medical virology, 2022-10, Vol.94 (10), p.4993-5006</ispartof><rights>2022 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2836-98eceab4d2c6a214d11ae000143214d4ddce05b3f3275af02424a0cea737cc153</citedby><cites>FETCH-LOGICAL-c2836-98eceab4d2c6a214d11ae000143214d4ddce05b3f3275af02424a0cea737cc153</cites><orcidid>0000-0001-6303-7642 ; 0000-0003-1075-6322</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.27926$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.27926$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35676468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhong, Shihong</creatorcontrib><creatorcontrib>Liu, Zhipeng</creatorcontrib><creatorcontrib>Zhou, Yang</creatorcontrib><creatorcontrib>Zhang, Tianling</creatorcontrib><creatorcontrib>Fu, Xin</creatorcontrib><creatorcontrib>Guo, Ling</creatorcontrib><creatorcontrib>Gu, Shuqin</creatorcontrib><creatorcontrib>Tang, Libo</creatorcontrib><creatorcontrib>Hou, Jinlin</creatorcontrib><creatorcontrib>Li, Yongyin</creatorcontrib><title>Longitudinal mapping of hepatitis B vaccine‐induced B‐cell linear epitopes in healthy individuals</title><title>Journal of medical virology</title><addtitle>J Med Virol</addtitle><description>The elimination of hepatitis B virus (HBV) infection is partially facilitated by the prophylactic HB vaccine. As the loss of seroprotection over time remains a conundrum for long‐lasting protection, a comprehensive dynamic analysis of immunogenic targets of the HB vaccine will provide novel insights into the improvement and design of potential targets. In this study, 36 healthy subjects without prior history of hepatitis B infection and negative for hepatitis B surface antibody (anti‐HBs) were enrolled. Participants were given a series of three doses of HB vaccine on a 0‐, 1‐, and 6‐month schedule and longitudinally followed up. We systematically mapped 55 overlapping 15‐mer peptides covering the small S protein of hepatitis B virus (SHBs) of vaccinees' serum samples at seven time points by performing an ELISA assay. Additionally, the frequencies and function dynamics of adaptive immune response were assessed by flow cytometry. We found that the SHBs peptide coverage presented an overall upward trend along with the vaccination progress, and the individual subpartition recognition was strongly correlated with the anti‐HBs titers. Moreover, we identified one dominant epitope (S29) located on “a determinant region” associated with effective vaccine response. Besides, significant correlations between the proportion of plasmablasts and proliferating B cells and levels of anti‐HBs were ascertained. Taken together, our data characterized the dynamics of HB vaccine‐induced neutralizing antibodies against B‐cell linear epitopes on SHBs and adaptive immune response, which will be constructive to develop the next‐generation vaccine.</description><subject>a determinant region</subject><subject>adaptive immune response</subject><subject>Adaptive immunity</subject><subject>Antibodies</subject><subject>B‐cell linear epitopes</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Epitope mapping</subject><subject>Flow cytometry</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>hepatitis B vaccination</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunogenicity</subject><subject>Infections</subject><subject>Lymphocytes B</subject><subject>peptide mapping</subject><subject>Peptides</subject><subject>Vaccination</subject><subject>Vaccines</subject><subject>Virology</subject><subject>Viruses</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kLtOwzAUhi0EoqUw8ALIEgsMKbbj2OlIK64qYgHWyLVPWle5ESdF3XgEnpEnwSWFAYnpHFvf-fXrQ-iYkiElhF0s89WQyRETO6hPyUgEIyLpLuoTykUgBI166MC5JSEkHjG2j3phJKTgIu4jmJbF3DatsYXKcK6qyhZzXKZ4AZVqbGMdHuOV0toW8Pn-YQvTajB47HcNWYYz_69qDJVtygoctoW_VFmzWPvV2JU1rcrcIdpL_YCj7Ryg5-urp8ltMH28uZtcTgPN4tDXjkGDmnHDtFCMckOpAt-a8nDz4sZoINEsTEMmI5USxhlXxJ_IUGpNo3CAzrrcqi5fW3BNklu36akKKFuXMCG5jLgUwqOnf9Bl2dZegqckYVJGjBJPnXeUrkvnakiTqra5qtcJJcnGfeLdJ9_uPXuyTWxnOZhf8ke2By464M1msP4_Kbl_eOkivwBPVZAW</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Zhong, Shihong</creator><creator>Liu, Zhipeng</creator><creator>Zhou, Yang</creator><creator>Zhang, Tianling</creator><creator>Fu, Xin</creator><creator>Guo, Ling</creator><creator>Gu, Shuqin</creator><creator>Tang, Libo</creator><creator>Hou, Jinlin</creator><creator>Li, Yongyin</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6303-7642</orcidid><orcidid>https://orcid.org/0000-0003-1075-6322</orcidid></search><sort><creationdate>202210</creationdate><title>Longitudinal mapping of hepatitis B vaccine‐induced B‐cell linear epitopes in healthy individuals</title><author>Zhong, Shihong ; Liu, Zhipeng ; Zhou, Yang ; Zhang, Tianling ; Fu, Xin ; Guo, Ling ; Gu, Shuqin ; Tang, Libo ; Hou, Jinlin ; Li, Yongyin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2836-98eceab4d2c6a214d11ae000143214d4ddce05b3f3275af02424a0cea737cc153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>a determinant region</topic><topic>adaptive immune response</topic><topic>Adaptive immunity</topic><topic>Antibodies</topic><topic>B‐cell linear epitopes</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Epitope mapping</topic><topic>Flow cytometry</topic><topic>Hepatitis</topic><topic>Hepatitis B</topic><topic>hepatitis B vaccination</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunogenicity</topic><topic>Infections</topic><topic>Lymphocytes B</topic><topic>peptide mapping</topic><topic>Peptides</topic><topic>Vaccination</topic><topic>Vaccines</topic><topic>Virology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhong, Shihong</creatorcontrib><creatorcontrib>Liu, Zhipeng</creatorcontrib><creatorcontrib>Zhou, Yang</creatorcontrib><creatorcontrib>Zhang, Tianling</creatorcontrib><creatorcontrib>Fu, Xin</creatorcontrib><creatorcontrib>Guo, Ling</creatorcontrib><creatorcontrib>Gu, Shuqin</creatorcontrib><creatorcontrib>Tang, Libo</creatorcontrib><creatorcontrib>Hou, Jinlin</creatorcontrib><creatorcontrib>Li, Yongyin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhong, Shihong</au><au>Liu, Zhipeng</au><au>Zhou, Yang</au><au>Zhang, Tianling</au><au>Fu, Xin</au><au>Guo, Ling</au><au>Gu, Shuqin</au><au>Tang, Libo</au><au>Hou, Jinlin</au><au>Li, Yongyin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal mapping of hepatitis B vaccine‐induced B‐cell linear epitopes in healthy individuals</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J Med Virol</addtitle><date>2022-10</date><risdate>2022</risdate><volume>94</volume><issue>10</issue><spage>4993</spage><epage>5006</epage><pages>4993-5006</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><abstract>The elimination of hepatitis B virus (HBV) infection is partially facilitated by the prophylactic HB vaccine. As the loss of seroprotection over time remains a conundrum for long‐lasting protection, a comprehensive dynamic analysis of immunogenic targets of the HB vaccine will provide novel insights into the improvement and design of potential targets. In this study, 36 healthy subjects without prior history of hepatitis B infection and negative for hepatitis B surface antibody (anti‐HBs) were enrolled. Participants were given a series of three doses of HB vaccine on a 0‐, 1‐, and 6‐month schedule and longitudinally followed up. We systematically mapped 55 overlapping 15‐mer peptides covering the small S protein of hepatitis B virus (SHBs) of vaccinees' serum samples at seven time points by performing an ELISA assay. Additionally, the frequencies and function dynamics of adaptive immune response were assessed by flow cytometry. We found that the SHBs peptide coverage presented an overall upward trend along with the vaccination progress, and the individual subpartition recognition was strongly correlated with the anti‐HBs titers. Moreover, we identified one dominant epitope (S29) located on “a determinant region” associated with effective vaccine response. Besides, significant correlations between the proportion of plasmablasts and proliferating B cells and levels of anti‐HBs were ascertained. Taken together, our data characterized the dynamics of HB vaccine‐induced neutralizing antibodies against B‐cell linear epitopes on SHBs and adaptive immune response, which will be constructive to develop the next‐generation vaccine.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35676468</pmid><doi>10.1002/jmv.27926</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-6303-7642</orcidid><orcidid>https://orcid.org/0000-0003-1075-6322</orcidid></addata></record> |
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subjects | a determinant region adaptive immune response Adaptive immunity Antibodies B‐cell linear epitopes Enzyme-linked immunosorbent assay Epitope mapping Flow cytometry Hepatitis Hepatitis B hepatitis B vaccination Immune response Immune system Immunogenicity Infections Lymphocytes B peptide mapping Peptides Vaccination Vaccines Virology Viruses |
title | Longitudinal mapping of hepatitis B vaccine‐induced B‐cell linear epitopes in healthy individuals |
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