17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients
Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patien...
Ausführliche Beschreibung
Autor*in: |
Wieten, R.W. [verfasserIn] Goorhuis, A. [verfasserIn] Jonker, E.F.F. [verfasserIn] de Bree, G.J. [verfasserIn] de Visser, A.W. [verfasserIn] van Genderen, P.J.J. [verfasserIn] Remmerswaal, E.B.M. [verfasserIn] ten Berge, I.J.M. [verfasserIn] Visser, L.G. [verfasserIn] Grobusch, M.P. [verfasserIn] van Leeuwen, E.M.M. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2016 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Journal of infection - Amsterdam [u.a.] : Elsevier, 1979, 72 |
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Übergeordnetes Werk: |
volume:72 |
DOI / URN: |
10.1016/j.jinf.2016.02.017 |
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Katalog-ID: |
ELV029526663 |
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245 | 1 | 0 | |a 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients |
264 | 1 | |c 2016 | |
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520 | |a Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. | ||
650 | 4 | |a 17D yellow fever | |
650 | 4 | |a Vaccination | |
650 | 4 | |a Immune-compromised | |
700 | 1 | |a Goorhuis, A. |e verfasserin |4 aut | |
700 | 1 | |a Jonker, E.F.F. |e verfasserin |4 aut | |
700 | 1 | |a de Bree, G.J. |e verfasserin |4 aut | |
700 | 1 | |a de Visser, A.W. |e verfasserin |4 aut | |
700 | 1 | |a van Genderen, P.J.J. |e verfasserin |4 aut | |
700 | 1 | |a Remmerswaal, E.B.M. |e verfasserin |4 aut | |
700 | 1 | |a ten Berge, I.J.M. |e verfasserin |4 aut | |
700 | 1 | |a Visser, L.G. |e verfasserin |4 aut | |
700 | 1 | |a Grobusch, M.P. |e verfasserin |4 aut | |
700 | 1 | |a van Leeuwen, E.M.M. |e verfasserin |4 aut | |
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2016 |
allfields |
10.1016/j.jinf.2016.02.017 doi (DE-627)ELV029526663 (ELSEVIER)S0163-4453(16)00082-7 DE-627 ger DE-627 rda eng 610 VZ 44.75 bkl Wieten, R.W. verfasserin aut 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients 2016 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. 17D yellow fever Vaccination Immune-compromised Goorhuis, A. verfasserin aut Jonker, E.F.F. verfasserin aut de Bree, G.J. verfasserin aut de Visser, A.W. verfasserin aut van Genderen, P.J.J. verfasserin aut Remmerswaal, E.B.M. verfasserin aut ten Berge, I.J.M. verfasserin aut Visser, L.G. verfasserin aut Grobusch, M.P. verfasserin aut van Leeuwen, E.M.M. verfasserin aut Enthalten in Journal of infection Amsterdam [u.a.] : Elsevier, 1979 72 Online-Ressource (DE-627)320506436 (DE-600)2012883-6 (DE-576)104344717 1532-2742 nnns volume:72 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2056 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_2098 GBV_ILN_2106 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_2470 GBV_ILN_2507 GBV_ILN_2522 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_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.75 Infektionskrankheiten parasitäre Krankheiten Medizin VZ AR 72 |
spelling |
10.1016/j.jinf.2016.02.017 doi (DE-627)ELV029526663 (ELSEVIER)S0163-4453(16)00082-7 DE-627 ger DE-627 rda eng 610 VZ 44.75 bkl Wieten, R.W. verfasserin aut 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients 2016 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. 17D yellow fever Vaccination Immune-compromised Goorhuis, A. verfasserin aut Jonker, E.F.F. verfasserin aut de Bree, G.J. verfasserin aut de Visser, A.W. verfasserin aut van Genderen, P.J.J. verfasserin aut Remmerswaal, E.B.M. verfasserin aut ten Berge, I.J.M. verfasserin aut Visser, L.G. verfasserin aut Grobusch, M.P. verfasserin aut van Leeuwen, E.M.M. verfasserin aut Enthalten in Journal of infection Amsterdam [u.a.] : Elsevier, 1979 72 Online-Ressource (DE-627)320506436 (DE-600)2012883-6 (DE-576)104344717 1532-2742 nnns volume:72 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2056 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_2098 GBV_ILN_2106 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_2470 GBV_ILN_2507 GBV_ILN_2522 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_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.75 Infektionskrankheiten parasitäre Krankheiten Medizin VZ AR 72 |
allfields_unstemmed |
10.1016/j.jinf.2016.02.017 doi (DE-627)ELV029526663 (ELSEVIER)S0163-4453(16)00082-7 DE-627 ger DE-627 rda eng 610 VZ 44.75 bkl Wieten, R.W. verfasserin aut 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients 2016 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. 17D yellow fever Vaccination Immune-compromised Goorhuis, A. verfasserin aut Jonker, E.F.F. verfasserin aut de Bree, G.J. verfasserin aut de Visser, A.W. verfasserin aut van Genderen, P.J.J. verfasserin aut Remmerswaal, E.B.M. verfasserin aut ten Berge, I.J.M. verfasserin aut Visser, L.G. verfasserin aut Grobusch, M.P. verfasserin aut van Leeuwen, E.M.M. verfasserin aut Enthalten in Journal of infection Amsterdam [u.a.] : Elsevier, 1979 72 Online-Ressource (DE-627)320506436 (DE-600)2012883-6 (DE-576)104344717 1532-2742 nnns volume:72 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2056 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_2098 GBV_ILN_2106 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_2470 GBV_ILN_2507 GBV_ILN_2522 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_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.75 Infektionskrankheiten parasitäre Krankheiten Medizin VZ AR 72 |
allfieldsGer |
10.1016/j.jinf.2016.02.017 doi (DE-627)ELV029526663 (ELSEVIER)S0163-4453(16)00082-7 DE-627 ger DE-627 rda eng 610 VZ 44.75 bkl Wieten, R.W. verfasserin aut 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients 2016 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. 17D yellow fever Vaccination Immune-compromised Goorhuis, A. verfasserin aut Jonker, E.F.F. verfasserin aut de Bree, G.J. verfasserin aut de Visser, A.W. verfasserin aut van Genderen, P.J.J. verfasserin aut Remmerswaal, E.B.M. verfasserin aut ten Berge, I.J.M. verfasserin aut Visser, L.G. verfasserin aut Grobusch, M.P. verfasserin aut van Leeuwen, E.M.M. verfasserin aut Enthalten in Journal of infection Amsterdam [u.a.] : Elsevier, 1979 72 Online-Ressource (DE-627)320506436 (DE-600)2012883-6 (DE-576)104344717 1532-2742 nnns volume:72 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2056 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_2098 GBV_ILN_2106 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_2470 GBV_ILN_2507 GBV_ILN_2522 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_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.75 Infektionskrankheiten parasitäre Krankheiten Medizin VZ AR 72 |
allfieldsSound |
10.1016/j.jinf.2016.02.017 doi (DE-627)ELV029526663 (ELSEVIER)S0163-4453(16)00082-7 DE-627 ger DE-627 rda eng 610 VZ 44.75 bkl Wieten, R.W. verfasserin aut 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients 2016 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. 17D yellow fever Vaccination Immune-compromised Goorhuis, A. verfasserin aut Jonker, E.F.F. verfasserin aut de Bree, G.J. verfasserin aut de Visser, A.W. verfasserin aut van Genderen, P.J.J. verfasserin aut Remmerswaal, E.B.M. verfasserin aut ten Berge, I.J.M. verfasserin aut Visser, L.G. verfasserin aut Grobusch, M.P. verfasserin aut van Leeuwen, E.M.M. verfasserin aut Enthalten in Journal of infection Amsterdam [u.a.] : Elsevier, 1979 72 Online-Ressource (DE-627)320506436 (DE-600)2012883-6 (DE-576)104344717 1532-2742 nnns volume:72 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2056 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_2098 GBV_ILN_2106 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_2470 GBV_ILN_2507 GBV_ILN_2522 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_4335 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.75 Infektionskrankheiten parasitäre Krankheiten Medizin VZ AR 72 |
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Wieten, R.W. @@aut@@ Goorhuis, A. @@aut@@ Jonker, E.F.F. @@aut@@ de Bree, G.J. @@aut@@ de Visser, A.W. @@aut@@ van Genderen, P.J.J. @@aut@@ Remmerswaal, E.B.M. @@aut@@ ten Berge, I.J.M. @@aut@@ Visser, L.G. @@aut@@ Grobusch, M.P. @@aut@@ van Leeuwen, E.M.M. @@aut@@ |
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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">ELV029526663</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230927082439.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2016 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.jinf.2016.02.017</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV029526663</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0163-4453(16)00082-7</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">rda</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">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">44.75</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Wieten, R.W.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2016</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</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">Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. 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author |
Wieten, R.W. |
spellingShingle |
Wieten, R.W. ddc 610 bkl 44.75 misc 17D yellow fever misc Vaccination misc Immune-compromised 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients |
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610 VZ 44.75 bkl 17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients 17D yellow fever Vaccination Immune-compromised |
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ddc 610 bkl 44.75 misc 17D yellow fever misc Vaccination misc Immune-compromised |
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Journal of infection |
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17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients |
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17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients |
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Wieten, R.W. |
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Journal of infection |
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Journal of infection |
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2016 |
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Wieten, R.W. Goorhuis, A. Jonker, E.F.F. de Bree, G.J. de Visser, A.W. van Genderen, P.J.J. Remmerswaal, E.B.M. ten Berge, I.J.M. Visser, L.G. Grobusch, M.P. van Leeuwen, E.M.M. |
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72 |
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610 VZ 44.75 bkl |
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Elektronische Aufsätze |
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Wieten, R.W. |
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10.1016/j.jinf.2016.02.017 |
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610 |
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verfasserin |
title_sort |
17d yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients |
title_auth |
17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients |
abstract |
Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. |
abstractGer |
Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. |
abstract_unstemmed |
Background: The 17D live attenuated yellow fever (YF) vaccine is contra-indicated in immune-compromised individuals and may elicit a suboptimal immunologic response. The aim of this study is to assess whether long-term immune responses against the YF vaccine are impaired in immune-compromised patients.Materials and methods: Fifteen patients using different immunosuppressive drugs and 30 healthy individuals vaccinated 0–22 years ago were included. The serological response was measured using the plaque reduction neutralization test (PRNT). CD8+ and CD4+ T-cell responses were measured following proliferation and re-stimulation with YFV peptide pools. Phenotypic characteristics and cytokine responses of CD8+ T-cells were determined using class I tetramers.Results: The geometric mean titre of neutralizing antibodies was not different between the groups (p = 0.77). The presence of YFV-specific CD4+ and CD8+ T-cell did not differ between patients and healthy individuals (15/15, 100.0% vs. 29/30, 96.7%, p = 0.475). Time since vaccination correlated negatively with the number of YFV-specific CD8+ T-cells (r = −0.66, p = 0.0045). Percentages of early-differentiated memory cells increased (r = 0.67, p = 0.017) over time.Conclusion: These results imply that YF vaccination is effective despite certain immunosuppressive drug regimens. An early-differentiated memory-like phenotype persisted, which is associated with effective expansion upon re-encounter with antigen, suggesting a potent memory T-cell pool remains. |
collection_details |
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title_short |
17D yellow fever vaccine elicits comparable long-term immune responses in healthy individuals and immune-compromised patients |
remote_bool |
true |
author2 |
Goorhuis, A. Jonker, E.F.F. de Bree, G.J. de Visser, A.W. van Genderen, P.J.J. Remmerswaal, E.B.M. ten Berge, I.J.M. Visser, L.G. Grobusch, M.P. van Leeuwen, E.M.M. |
author2Str |
Goorhuis, A. Jonker, E.F.F. de Bree, G.J. de Visser, A.W. van Genderen, P.J.J. Remmerswaal, E.B.M. ten Berge, I.J.M. Visser, L.G. Grobusch, M.P. van Leeuwen, E.M.M. |
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doi_str |
10.1016/j.jinf.2016.02.017 |
up_date |
2024-07-06T21:41:47.014Z |
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