Immunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.

BACKGROUND: Measles vaccine in early infancy followed by a dose at 9 months of age protects against measles and enhances child survival through non-specific effects. Little is known of immune responses in the short or long term after booster doses. METHODS: Infants were randomized to receive measles...

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Hoofdauteurs: Njie-Jobe, J, Nyamweya, S, Miles, D, van der Sande, M, Zaman, S, Touray, E, Hossin, S, Adetifa, J, Palmero, M, Burl, S, Jeffries, D, Rowland-Jones, S, Flanagan, K, Jaye, A, Whittle, H
Formaat: Journal article
Taal:English
Gepubliceerd in: 2012
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author Njie-Jobe, J
Nyamweya, S
Miles, D
van der Sande, M
Zaman, S
Touray, E
Hossin, S
Adetifa, J
Palmero, M
Burl, S
Jeffries, D
Rowland-Jones, S
Flanagan, K
Jaye, A
Whittle, H
author_facet Njie-Jobe, J
Nyamweya, S
Miles, D
van der Sande, M
Zaman, S
Touray, E
Hossin, S
Adetifa, J
Palmero, M
Burl, S
Jeffries, D
Rowland-Jones, S
Flanagan, K
Jaye, A
Whittle, H
author_sort Njie-Jobe, J
collection OXFORD
description BACKGROUND: Measles vaccine in early infancy followed by a dose at 9 months of age protects against measles and enhances child survival through non-specific effects. Little is known of immune responses in the short or long term after booster doses. METHODS: Infants were randomized to receive measles vaccine at 9 months of age (group 1) or 4 and 9 months of age (group 2). Both groups received a boost at 36 months of age. T-cell effector and memory responses using IFN-γ ELIspot and cytokine assays and antibody titres using a haemagglutination-inhibition assay were compared at various times. RESULTS: Vaccination at 4 months of age elicited antibody and CD4 T-cell mediated immune responses .Two weeks after vaccination at 9 months of age group 2 had much higher antibody titres than group1 infants; cell-mediated effector responses were similar. At 36 months of age group 2 antibody titres exceeded protective levels but were 4-fold lower than group 1; effector and cytokine responses were similar. Re-vaccination resulted in similar rapid and high antibody titres in both groups (median 512); cellular immunity changed little. At 48 months of age group 2 antibody concentrations remained well above protective levels though 2-fold lower than group 1; T-cell memory was readily detectable and similar in both groups. CONCLUSIONS: An additional early measles vaccine given to children at 4 months of age induced a predominant CD4 T-cell response at 9 months and rapid development of high antibody concentrations after booster doses. However, antibody decayed faster in these children than in the group given primary vaccination at 9 months of age. Cellular responses after 9 months were generally insignificantly different.
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spelling oxford-uuid:57f86f50-b2ce-4001-b84f-574a88a1ad9c2022-03-26T17:00:04ZImmunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:57f86f50-b2ce-4001-b84f-574a88a1ad9cEnglishSymplectic Elements at Oxford2012Njie-Jobe, JNyamweya, SMiles, Dvan der Sande, MZaman, STouray, EHossin, SAdetifa, JPalmero, MBurl, SJeffries, DRowland-Jones, SFlanagan, KJaye, AWhittle, HBACKGROUND: Measles vaccine in early infancy followed by a dose at 9 months of age protects against measles and enhances child survival through non-specific effects. Little is known of immune responses in the short or long term after booster doses. METHODS: Infants were randomized to receive measles vaccine at 9 months of age (group 1) or 4 and 9 months of age (group 2). Both groups received a boost at 36 months of age. T-cell effector and memory responses using IFN-γ ELIspot and cytokine assays and antibody titres using a haemagglutination-inhibition assay were compared at various times. RESULTS: Vaccination at 4 months of age elicited antibody and CD4 T-cell mediated immune responses .Two weeks after vaccination at 9 months of age group 2 had much higher antibody titres than group1 infants; cell-mediated effector responses were similar. At 36 months of age group 2 antibody titres exceeded protective levels but were 4-fold lower than group 1; effector and cytokine responses were similar. Re-vaccination resulted in similar rapid and high antibody titres in both groups (median 512); cellular immunity changed little. At 48 months of age group 2 antibody concentrations remained well above protective levels though 2-fold lower than group 1; T-cell memory was readily detectable and similar in both groups. CONCLUSIONS: An additional early measles vaccine given to children at 4 months of age induced a predominant CD4 T-cell response at 9 months and rapid development of high antibody concentrations after booster doses. However, antibody decayed faster in these children than in the group given primary vaccination at 9 months of age. Cellular responses after 9 months were generally insignificantly different.
spellingShingle Njie-Jobe, J
Nyamweya, S
Miles, D
van der Sande, M
Zaman, S
Touray, E
Hossin, S
Adetifa, J
Palmero, M
Burl, S
Jeffries, D
Rowland-Jones, S
Flanagan, K
Jaye, A
Whittle, H
Immunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.
title Immunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.
title_full Immunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.
title_fullStr Immunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.
title_full_unstemmed Immunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.
title_short Immunological impact of an additional early measles vaccine in Gambian children: responses to a boost at 3 years.
title_sort immunological impact of an additional early measles vaccine in gambian children responses to a boost at 3 years
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