Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins
Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immuni...
Ausführliche Beschreibung
Autor*in: |
Bernardo, Lidice [verfasserIn] Hermida, Lisset [verfasserIn] Martin, Jorge [verfasserIn] Alvarez, Mayling [verfasserIn] Prado, Irina [verfasserIn] López, Carlos [verfasserIn] Martínez, Rafael [verfasserIn] Rodríguez-Roche, Rosmari [verfasserIn] Zulueta, Aida [verfasserIn] Lazo, Laura [verfasserIn] Rosario, Delfina [verfasserIn] Guillén, Gerardo [verfasserIn] Guzmán, María G. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2008 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Archives of virology - Wien : Springer, 1939, 153(2008), 5 vom: 26. Feb., Seite 849-854 |
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Übergeordnetes Werk: |
volume:153 ; year:2008 ; number:5 ; day:26 ; month:02 ; pages:849-854 |
Links: |
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DOI / URN: |
10.1007/s00705-008-0050-9 |
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Katalog-ID: |
SPR007383371 |
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245 | 1 | 0 | |a Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins |
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520 | |a Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. | ||
650 | 4 | |a Viral Challenge |7 (dpeaa)DE-He213 | |
650 | 4 | |a DENV Infection |7 (dpeaa)DE-He213 | |
650 | 4 | |a Recombinant Fusion Protein |7 (dpeaa)DE-He213 | |
650 | 4 | |a Neutralize Antibody Titer |7 (dpeaa)DE-He213 | |
650 | 4 | |a Dengue Vaccine |7 (dpeaa)DE-He213 | |
700 | 1 | |a Hermida, Lisset |e verfasserin |4 aut | |
700 | 1 | |a Martin, Jorge |e verfasserin |4 aut | |
700 | 1 | |a Alvarez, Mayling |e verfasserin |4 aut | |
700 | 1 | |a Prado, Irina |e verfasserin |4 aut | |
700 | 1 | |a López, Carlos |e verfasserin |4 aut | |
700 | 1 | |a Martínez, Rafael |e verfasserin |4 aut | |
700 | 1 | |a Rodríguez-Roche, Rosmari |e verfasserin |4 aut | |
700 | 1 | |a Zulueta, Aida |e verfasserin |4 aut | |
700 | 1 | |a Lazo, Laura |e verfasserin |4 aut | |
700 | 1 | |a Rosario, Delfina |e verfasserin |4 aut | |
700 | 1 | |a Guillén, Gerardo |e verfasserin |4 aut | |
700 | 1 | |a Guzmán, María G. |e verfasserin |4 aut | |
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10.1007/s00705-008-0050-9 doi (DE-627)SPR007383371 (SPR)s00705-008-0050-9-e DE-627 ger DE-627 rakwb eng 610 ASE 42.32 bkl 44.43 bkl Bernardo, Lidice verfasserin aut Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. Viral Challenge (dpeaa)DE-He213 DENV Infection (dpeaa)DE-He213 Recombinant Fusion Protein (dpeaa)DE-He213 Neutralize Antibody Titer (dpeaa)DE-He213 Dengue Vaccine (dpeaa)DE-He213 Hermida, Lisset verfasserin aut Martin, Jorge verfasserin aut Alvarez, Mayling verfasserin aut Prado, Irina verfasserin aut López, Carlos verfasserin aut Martínez, Rafael verfasserin aut Rodríguez-Roche, Rosmari verfasserin aut Zulueta, Aida verfasserin aut Lazo, Laura verfasserin aut Rosario, Delfina verfasserin aut Guillén, Gerardo verfasserin aut Guzmán, María G. verfasserin aut Enthalten in Archives of virology Wien : Springer, 1939 153(2008), 5 vom: 26. Feb., Seite 849-854 (DE-627)253390168 (DE-600)1458460-8 1432-8798 nnns volume:153 year:2008 number:5 day:26 month:02 pages:849-854 https://dx.doi.org/10.1007/s00705-008-0050-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.32 ASE 44.43 ASE AR 153 2008 5 26 02 849-854 |
spelling |
10.1007/s00705-008-0050-9 doi (DE-627)SPR007383371 (SPR)s00705-008-0050-9-e DE-627 ger DE-627 rakwb eng 610 ASE 42.32 bkl 44.43 bkl Bernardo, Lidice verfasserin aut Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. Viral Challenge (dpeaa)DE-He213 DENV Infection (dpeaa)DE-He213 Recombinant Fusion Protein (dpeaa)DE-He213 Neutralize Antibody Titer (dpeaa)DE-He213 Dengue Vaccine (dpeaa)DE-He213 Hermida, Lisset verfasserin aut Martin, Jorge verfasserin aut Alvarez, Mayling verfasserin aut Prado, Irina verfasserin aut López, Carlos verfasserin aut Martínez, Rafael verfasserin aut Rodríguez-Roche, Rosmari verfasserin aut Zulueta, Aida verfasserin aut Lazo, Laura verfasserin aut Rosario, Delfina verfasserin aut Guillén, Gerardo verfasserin aut Guzmán, María G. verfasserin aut Enthalten in Archives of virology Wien : Springer, 1939 153(2008), 5 vom: 26. Feb., Seite 849-854 (DE-627)253390168 (DE-600)1458460-8 1432-8798 nnns volume:153 year:2008 number:5 day:26 month:02 pages:849-854 https://dx.doi.org/10.1007/s00705-008-0050-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.32 ASE 44.43 ASE AR 153 2008 5 26 02 849-854 |
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10.1007/s00705-008-0050-9 doi (DE-627)SPR007383371 (SPR)s00705-008-0050-9-e DE-627 ger DE-627 rakwb eng 610 ASE 42.32 bkl 44.43 bkl Bernardo, Lidice verfasserin aut Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. Viral Challenge (dpeaa)DE-He213 DENV Infection (dpeaa)DE-He213 Recombinant Fusion Protein (dpeaa)DE-He213 Neutralize Antibody Titer (dpeaa)DE-He213 Dengue Vaccine (dpeaa)DE-He213 Hermida, Lisset verfasserin aut Martin, Jorge verfasserin aut Alvarez, Mayling verfasserin aut Prado, Irina verfasserin aut López, Carlos verfasserin aut Martínez, Rafael verfasserin aut Rodríguez-Roche, Rosmari verfasserin aut Zulueta, Aida verfasserin aut Lazo, Laura verfasserin aut Rosario, Delfina verfasserin aut Guillén, Gerardo verfasserin aut Guzmán, María G. verfasserin aut Enthalten in Archives of virology Wien : Springer, 1939 153(2008), 5 vom: 26. Feb., Seite 849-854 (DE-627)253390168 (DE-600)1458460-8 1432-8798 nnns volume:153 year:2008 number:5 day:26 month:02 pages:849-854 https://dx.doi.org/10.1007/s00705-008-0050-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.32 ASE 44.43 ASE AR 153 2008 5 26 02 849-854 |
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10.1007/s00705-008-0050-9 doi (DE-627)SPR007383371 (SPR)s00705-008-0050-9-e DE-627 ger DE-627 rakwb eng 610 ASE 42.32 bkl 44.43 bkl Bernardo, Lidice verfasserin aut Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. Viral Challenge (dpeaa)DE-He213 DENV Infection (dpeaa)DE-He213 Recombinant Fusion Protein (dpeaa)DE-He213 Neutralize Antibody Titer (dpeaa)DE-He213 Dengue Vaccine (dpeaa)DE-He213 Hermida, Lisset verfasserin aut Martin, Jorge verfasserin aut Alvarez, Mayling verfasserin aut Prado, Irina verfasserin aut López, Carlos verfasserin aut Martínez, Rafael verfasserin aut Rodríguez-Roche, Rosmari verfasserin aut Zulueta, Aida verfasserin aut Lazo, Laura verfasserin aut Rosario, Delfina verfasserin aut Guillén, Gerardo verfasserin aut Guzmán, María G. verfasserin aut Enthalten in Archives of virology Wien : Springer, 1939 153(2008), 5 vom: 26. Feb., Seite 849-854 (DE-627)253390168 (DE-600)1458460-8 1432-8798 nnns volume:153 year:2008 number:5 day:26 month:02 pages:849-854 https://dx.doi.org/10.1007/s00705-008-0050-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.32 ASE 44.43 ASE AR 153 2008 5 26 02 849-854 |
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10.1007/s00705-008-0050-9 doi (DE-627)SPR007383371 (SPR)s00705-008-0050-9-e DE-627 ger DE-627 rakwb eng 610 ASE 42.32 bkl 44.43 bkl Bernardo, Lidice verfasserin aut Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. Viral Challenge (dpeaa)DE-He213 DENV Infection (dpeaa)DE-He213 Recombinant Fusion Protein (dpeaa)DE-He213 Neutralize Antibody Titer (dpeaa)DE-He213 Dengue Vaccine (dpeaa)DE-He213 Hermida, Lisset verfasserin aut Martin, Jorge verfasserin aut Alvarez, Mayling verfasserin aut Prado, Irina verfasserin aut López, Carlos verfasserin aut Martínez, Rafael verfasserin aut Rodríguez-Roche, Rosmari verfasserin aut Zulueta, Aida verfasserin aut Lazo, Laura verfasserin aut Rosario, Delfina verfasserin aut Guillén, Gerardo verfasserin aut Guzmán, María G. verfasserin aut Enthalten in Archives of virology Wien : Springer, 1939 153(2008), 5 vom: 26. Feb., Seite 849-854 (DE-627)253390168 (DE-600)1458460-8 1432-8798 nnns volume:153 year:2008 number:5 day:26 month:02 pages:849-854 https://dx.doi.org/10.1007/s00705-008-0050-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_252 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.32 ASE 44.43 ASE AR 153 2008 5 26 02 849-854 |
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Enthalten in Archives of virology 153(2008), 5 vom: 26. Feb., Seite 849-854 volume:153 year:2008 number:5 day:26 month:02 pages:849-854 |
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Enthalten in Archives of virology 153(2008), 5 vom: 26. Feb., Seite 849-854 volume:153 year:2008 number:5 day:26 month:02 pages:849-854 |
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Viral Challenge DENV Infection Recombinant Fusion Protein Neutralize Antibody Titer Dengue Vaccine |
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Bernardo, Lidice @@aut@@ Hermida, Lisset @@aut@@ Martin, Jorge @@aut@@ Alvarez, Mayling @@aut@@ Prado, Irina @@aut@@ López, Carlos @@aut@@ Martínez, Rafael @@aut@@ Rodríguez-Roche, Rosmari @@aut@@ Zulueta, Aida @@aut@@ Lazo, Laura @@aut@@ Rosario, Delfina @@aut@@ Guillén, Gerardo @@aut@@ Guzmán, María G. @@aut@@ |
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2008-02-26T00:00:00Z |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR007383371</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519082225.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201005s2008 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s00705-008-0050-9</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR007383371</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s00705-008-0050-9-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">42.32</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">44.43</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Bernardo, Lidice</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2008</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Viral Challenge</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">DENV Infection</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Recombinant Fusion Protein</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Neutralize Antibody Titer</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Dengue Vaccine</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hermida, Lisset</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Martin, Jorge</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Alvarez, Mayling</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Prado, Irina</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">López, Carlos</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Martínez, Rafael</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Rodríguez-Roche, Rosmari</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zulueta, Aida</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Lazo, Laura</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Rosario, Delfina</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Guillén, Gerardo</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Guzmán, María G.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Archives of virology</subfield><subfield code="d">Wien : Springer, 1939</subfield><subfield code="g">153(2008), 5 vom: 26. 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|
author |
Bernardo, Lidice |
spellingShingle |
Bernardo, Lidice ddc 610 bkl 42.32 bkl 44.43 misc Viral Challenge misc DENV Infection misc Recombinant Fusion Protein misc Neutralize Antibody Titer misc Dengue Vaccine Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins |
authorStr |
Bernardo, Lidice |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)253390168 |
format |
electronic Article |
dewey-ones |
610 - Medicine & health |
delete_txt_mv |
keep |
author_role |
aut aut aut aut aut aut aut aut aut aut aut aut aut |
collection |
springer |
remote_str |
true |
illustrated |
Not Illustrated |
issn |
1432-8798 |
topic_title |
610 ASE 42.32 bkl 44.43 bkl Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins Viral Challenge (dpeaa)DE-He213 DENV Infection (dpeaa)DE-He213 Recombinant Fusion Protein (dpeaa)DE-He213 Neutralize Antibody Titer (dpeaa)DE-He213 Dengue Vaccine (dpeaa)DE-He213 |
topic |
ddc 610 bkl 42.32 bkl 44.43 misc Viral Challenge misc DENV Infection misc Recombinant Fusion Protein misc Neutralize Antibody Titer misc Dengue Vaccine |
topic_unstemmed |
ddc 610 bkl 42.32 bkl 44.43 misc Viral Challenge misc DENV Infection misc Recombinant Fusion Protein misc Neutralize Antibody Titer misc Dengue Vaccine |
topic_browse |
ddc 610 bkl 42.32 bkl 44.43 misc Viral Challenge misc DENV Infection misc Recombinant Fusion Protein misc Neutralize Antibody Titer misc Dengue Vaccine |
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Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins |
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Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins |
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Bernardo, Lidice |
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eng |
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Bernardo, Lidice Hermida, Lisset Martin, Jorge Alvarez, Mayling Prado, Irina López, Carlos Martínez, Rafael Rodríguez-Roche, Rosmari Zulueta, Aida Lazo, Laura Rosario, Delfina Guillén, Gerardo Guzmán, María G. |
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anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins |
title_auth |
Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins |
abstract |
Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. |
abstractGer |
Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. |
abstract_unstemmed |
Abstract The suitability of dengue 2 envelope domain III recombinant fusion proteins [(fusion (PD5) and insertion (PD3) variants)] for inducing functional antibodies and a protective immune response in nonhuman primates has been reported. However, the evaluation of the antibody response after immunization did not correlate with the protection data as measured by viremia detection. Here, we characterized the anamnestic immune response after viral challenge in monkeys immunized with the dengue 2 recombinant proteins in an attempt to define correlates of protection useful for vaccine studies. Monkeys immunized with PD5 (most protected group) exhibited an earlier increase in the anti-DENV-2 IgM response after challenge compared to control animals. Hemagglutination-inhibiting (HAI) antibodies were increased significantly earlier in PD5-immunized animals compared to those immunized with PD3. The fully protected monkeys showed the earliest HAI antibody response. These results underline the usefulness of the anamnestic antibody response for supporting protection data. The induction of an early HAI and IgM antibody response after challenge suggest a protective role against dengue virus (DENV) infection in monkeys, supporting their use as correlates of protection in vaccine studies. |
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title_short |
Anamnestic antibody response after viral challenge in monkeys immunized with dengue 2 recombinant fusion proteins |
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https://dx.doi.org/10.1007/s00705-008-0050-9 |
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Hermida, Lisset Martin, Jorge Alvarez, Mayling Prado, Irina López, Carlos Martínez, Rafael Rodríguez-Roche, Rosmari Zulueta, Aida Lazo, Laura Rosario, Delfina Guillén, Gerardo Guzmán, María G. |
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Hermida, Lisset Martin, Jorge Alvarez, Mayling Prado, Irina López, Carlos Martínez, Rafael Rodríguez-Roche, Rosmari Zulueta, Aida Lazo, Laura Rosario, Delfina Guillén, Gerardo Guzmán, María G. |
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up_date |
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|
score |
7.398464 |