Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response
ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese...
Ausführliche Beschreibung
Autor*in: |
Anna E. Coghill [verfasserIn] Jianwen Fang [verfasserIn] Zhiwei Liu [verfasserIn] Chien-Jen Chen [verfasserIn] Ruth F. Jarrett [verfasserIn] Henrik Hjalgrim [verfasserIn] Carla Proietti [verfasserIn] Kelly J. Yu [verfasserIn] Wan-Lun Hsu [verfasserIn] Pei-Jen Lou [verfasserIn] Chen-Ping Wang [verfasserIn] Yingdong Zhao [verfasserIn] Denise L. Doolan [verfasserIn] Allan Hildesheim [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2022 |
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Übergeordnetes Werk: |
In: International Journal of Infectious Diseases - Elsevier, 2015, 114(2022), Seite 65-71 |
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Übergeordnetes Werk: |
volume:114 ; year:2022 ; pages:65-71 |
Links: |
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DOI / URN: |
10.1016/j.ijid.2021.10.054 |
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Katalog-ID: |
DOAJ063435195 |
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520 | |a ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. | ||
650 | 4 | |a Epstein–Barr virus | |
650 | 4 | |a IgG antibody array | |
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650 | 4 | |a EBNA protein | |
653 | 0 | |a Infectious and parasitic diseases | |
700 | 0 | |a Jianwen Fang |e verfasserin |4 aut | |
700 | 0 | |a Zhiwei Liu |e verfasserin |4 aut | |
700 | 0 | |a Chien-Jen Chen |e verfasserin |4 aut | |
700 | 0 | |a Ruth F. Jarrett |e verfasserin |4 aut | |
700 | 0 | |a Henrik Hjalgrim |e verfasserin |4 aut | |
700 | 0 | |a Carla Proietti |e verfasserin |4 aut | |
700 | 0 | |a Kelly J. Yu |e verfasserin |4 aut | |
700 | 0 | |a Wan-Lun Hsu |e verfasserin |4 aut | |
700 | 0 | |a Pei-Jen Lou |e verfasserin |4 aut | |
700 | 0 | |a Chen-Ping Wang |e verfasserin |4 aut | |
700 | 0 | |a Yingdong Zhao |e verfasserin |4 aut | |
700 | 0 | |a Denise L. Doolan |e verfasserin |4 aut | |
700 | 0 | |a Allan Hildesheim |e verfasserin |4 aut | |
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10.1016/j.ijid.2021.10.054 doi (DE-627)DOAJ063435195 (DE-599)DOAJbb033c0992f74958a4dbcc75d7993452 DE-627 ger DE-627 rakwb eng RC109-216 Anna E. Coghill verfasserin aut Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. Epstein–Barr virus IgG antibody array LMP1/2 EBNA protein Infectious and parasitic diseases Jianwen Fang verfasserin aut Zhiwei Liu verfasserin aut Chien-Jen Chen verfasserin aut Ruth F. Jarrett verfasserin aut Henrik Hjalgrim verfasserin aut Carla Proietti verfasserin aut Kelly J. Yu verfasserin aut Wan-Lun Hsu verfasserin aut Pei-Jen Lou verfasserin aut Chen-Ping Wang verfasserin aut Yingdong Zhao verfasserin aut Denise L. Doolan verfasserin aut Allan Hildesheim verfasserin aut In International Journal of Infectious Diseases Elsevier, 2015 114(2022), Seite 65-71 (DE-627)341907669 (DE-600)2070533-5 18783511 nnns volume:114 year:2022 pages:65-71 https://doi.org/10.1016/j.ijid.2021.10.054 kostenfrei https://doaj.org/article/bb033c0992f74958a4dbcc75d7993452 kostenfrei http://www.sciencedirect.com/science/article/pii/S1201971221008420 kostenfrei https://doaj.org/toc/1201-9712 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 114 2022 65-71 |
spelling |
10.1016/j.ijid.2021.10.054 doi (DE-627)DOAJ063435195 (DE-599)DOAJbb033c0992f74958a4dbcc75d7993452 DE-627 ger DE-627 rakwb eng RC109-216 Anna E. Coghill verfasserin aut Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. Epstein–Barr virus IgG antibody array LMP1/2 EBNA protein Infectious and parasitic diseases Jianwen Fang verfasserin aut Zhiwei Liu verfasserin aut Chien-Jen Chen verfasserin aut Ruth F. Jarrett verfasserin aut Henrik Hjalgrim verfasserin aut Carla Proietti verfasserin aut Kelly J. Yu verfasserin aut Wan-Lun Hsu verfasserin aut Pei-Jen Lou verfasserin aut Chen-Ping Wang verfasserin aut Yingdong Zhao verfasserin aut Denise L. Doolan verfasserin aut Allan Hildesheim verfasserin aut In International Journal of Infectious Diseases Elsevier, 2015 114(2022), Seite 65-71 (DE-627)341907669 (DE-600)2070533-5 18783511 nnns volume:114 year:2022 pages:65-71 https://doi.org/10.1016/j.ijid.2021.10.054 kostenfrei https://doaj.org/article/bb033c0992f74958a4dbcc75d7993452 kostenfrei http://www.sciencedirect.com/science/article/pii/S1201971221008420 kostenfrei https://doaj.org/toc/1201-9712 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 114 2022 65-71 |
allfields_unstemmed |
10.1016/j.ijid.2021.10.054 doi (DE-627)DOAJ063435195 (DE-599)DOAJbb033c0992f74958a4dbcc75d7993452 DE-627 ger DE-627 rakwb eng RC109-216 Anna E. Coghill verfasserin aut Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. Epstein–Barr virus IgG antibody array LMP1/2 EBNA protein Infectious and parasitic diseases Jianwen Fang verfasserin aut Zhiwei Liu verfasserin aut Chien-Jen Chen verfasserin aut Ruth F. Jarrett verfasserin aut Henrik Hjalgrim verfasserin aut Carla Proietti verfasserin aut Kelly J. Yu verfasserin aut Wan-Lun Hsu verfasserin aut Pei-Jen Lou verfasserin aut Chen-Ping Wang verfasserin aut Yingdong Zhao verfasserin aut Denise L. Doolan verfasserin aut Allan Hildesheim verfasserin aut In International Journal of Infectious Diseases Elsevier, 2015 114(2022), Seite 65-71 (DE-627)341907669 (DE-600)2070533-5 18783511 nnns volume:114 year:2022 pages:65-71 https://doi.org/10.1016/j.ijid.2021.10.054 kostenfrei https://doaj.org/article/bb033c0992f74958a4dbcc75d7993452 kostenfrei http://www.sciencedirect.com/science/article/pii/S1201971221008420 kostenfrei https://doaj.org/toc/1201-9712 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 114 2022 65-71 |
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10.1016/j.ijid.2021.10.054 doi (DE-627)DOAJ063435195 (DE-599)DOAJbb033c0992f74958a4dbcc75d7993452 DE-627 ger DE-627 rakwb eng RC109-216 Anna E. Coghill verfasserin aut Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. Epstein–Barr virus IgG antibody array LMP1/2 EBNA protein Infectious and parasitic diseases Jianwen Fang verfasserin aut Zhiwei Liu verfasserin aut Chien-Jen Chen verfasserin aut Ruth F. Jarrett verfasserin aut Henrik Hjalgrim verfasserin aut Carla Proietti verfasserin aut Kelly J. Yu verfasserin aut Wan-Lun Hsu verfasserin aut Pei-Jen Lou verfasserin aut Chen-Ping Wang verfasserin aut Yingdong Zhao verfasserin aut Denise L. Doolan verfasserin aut Allan Hildesheim verfasserin aut In International Journal of Infectious Diseases Elsevier, 2015 114(2022), Seite 65-71 (DE-627)341907669 (DE-600)2070533-5 18783511 nnns volume:114 year:2022 pages:65-71 https://doi.org/10.1016/j.ijid.2021.10.054 kostenfrei https://doaj.org/article/bb033c0992f74958a4dbcc75d7993452 kostenfrei http://www.sciencedirect.com/science/article/pii/S1201971221008420 kostenfrei https://doaj.org/toc/1201-9712 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 114 2022 65-71 |
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10.1016/j.ijid.2021.10.054 doi (DE-627)DOAJ063435195 (DE-599)DOAJbb033c0992f74958a4dbcc75d7993452 DE-627 ger DE-627 rakwb eng RC109-216 Anna E. Coghill verfasserin aut Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. Epstein–Barr virus IgG antibody array LMP1/2 EBNA protein Infectious and parasitic diseases Jianwen Fang verfasserin aut Zhiwei Liu verfasserin aut Chien-Jen Chen verfasserin aut Ruth F. Jarrett verfasserin aut Henrik Hjalgrim verfasserin aut Carla Proietti verfasserin aut Kelly J. Yu verfasserin aut Wan-Lun Hsu verfasserin aut Pei-Jen Lou verfasserin aut Chen-Ping Wang verfasserin aut Yingdong Zhao verfasserin aut Denise L. Doolan verfasserin aut Allan Hildesheim verfasserin aut In International Journal of Infectious Diseases Elsevier, 2015 114(2022), Seite 65-71 (DE-627)341907669 (DE-600)2070533-5 18783511 nnns volume:114 year:2022 pages:65-71 https://doi.org/10.1016/j.ijid.2021.10.054 kostenfrei https://doaj.org/article/bb033c0992f74958a4dbcc75d7993452 kostenfrei http://www.sciencedirect.com/science/article/pii/S1201971221008420 kostenfrei https://doaj.org/toc/1201-9712 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 114 2022 65-71 |
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R - Medicine |
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Anna E. Coghill |
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Anna E. Coghill misc RC109-216 misc Epstein–Barr virus misc IgG antibody array misc LMP1/2 misc EBNA protein misc Infectious and parasitic diseases Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response |
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RC109-216 Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response Epstein–Barr virus IgG antibody array LMP1/2 EBNA protein |
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Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response |
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Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response |
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Anna E. Coghill |
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Anna E. Coghill Jianwen Fang Zhiwei Liu Chien-Jen Chen Ruth F. Jarrett Henrik Hjalgrim Carla Proietti Kelly J. Yu Wan-Lun Hsu Pei-Jen Lou Chen-Ping Wang Yingdong Zhao Denise L. Doolan Allan Hildesheim |
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identifying epstein–barr virus peptide sequences associated with differential igg antibody response |
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RC109-216 |
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Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response |
abstract |
ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. |
abstractGer |
ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. |
abstract_unstemmed |
ABSTRACT: Background: Epstein–Barr virus (EBV) infection contributes to cancers in a fraction of seropositive individuals, but much remains to be learned about variation in EBV-directed humoral immunity in cancer-free adults. Methods: A protein microarray was used to probe serum from 175 Taiwanese and 141 Northern European adults for immunoglobulin G (IgG) antibody responses to 115 different peptide sequences, representing protein segments or protein variants, from 45 EBV proteins. It was posited that this antibody-based approach could identify EBV peptide sequences representing immunodominant regions relevant for B-cell immunity. Results: Analyses of 45 EBV proteins with multiple protein segments or variants printed on the array identified eight EBV peptide sequences that appear to play a role in immunogenicity. This included: (1) three proteins with segments/regions associated with IgG reactivity (BALF5, LMP1, LMP2A); and (2) five proteins with sequence variants/amino acid changes associated with IgG reactivity (BDLF4, EBNA3A, EBNA3B, EBNA-LP, LF1). Conclusion: This examination of IgG antibody responses against 115 EBV peptide sequences in 316 cancer-free adults represents an important step toward identifying specific EBV protein sequences that play a role in generating B-cell immunity in humans. |
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title_short |
Identifying Epstein–Barr virus peptide sequences associated with differential IgG antibody response |
url |
https://doi.org/10.1016/j.ijid.2021.10.054 https://doaj.org/article/bb033c0992f74958a4dbcc75d7993452 http://www.sciencedirect.com/science/article/pii/S1201971221008420 https://doaj.org/toc/1201-9712 |
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Jianwen Fang Zhiwei Liu Chien-Jen Chen Ruth F. Jarrett Henrik Hjalgrim Carla Proietti Kelly J. Yu Wan-Lun Hsu Pei-Jen Lou Chen-Ping Wang Yingdong Zhao Denise L. Doolan Allan Hildesheim |
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Jianwen Fang Zhiwei Liu Chien-Jen Chen Ruth F. Jarrett Henrik Hjalgrim Carla Proietti Kelly J. Yu Wan-Lun Hsu Pei-Jen Lou Chen-Ping Wang Yingdong Zhao Denise L. Doolan Allan Hildesheim |
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