Impact of ageing and a synbiotic on the immune response to seasonal influenza vaccination; a randomised controlled trial
Impact of ageing and a synbiotic on the immune response to seasonal influenza vaccination; a randomised controlled trial
Background & Aims: Ageing increases risk of respiratory infections and impairs the response to influenza vaccination. Pre- and probiotics offer an opportunity to modulate anti-viral defenses and the response to vaccination via alteration of the gut microbiota. This study investigated the effect of a novel probiotic, Bifidobacterium longum bv. infantis CCUG 52486, combined with a prebiotic, gluco-oligosaccharide, on the B and T cell response to seasonal influenza vaccination in young and older subjects.
Methods: In a double-blind, randomized controlled trial, 58 young (18-35y) and 54 older (60-85y) subjects were supplemented with the synbiotic for 8 weeks. At 4 weeks they were administered with a seasonal influenza vaccine. B and T cell phenotype and responsiveness to in vitro re-stimulation with the vaccine were assessed at baseline, 4, 6 and 8 weeks.
Results: B and T cell profiles differed markedly between young and older subjects. Vaccination increased numbers of memory, IgA+ memory, IgG+ memory and total IgG+ B cells in young subjects, but failed to do so in older subjects and did not significantly alter T cell subsets. Seroconversion to the H1N1 subunit in the older subjects was associated with higher post38 vaccination numbers of plasma B cells, but seroconversion was less consistently associated with T cell phenotype. B and T cell subsets from both young and older subjects demonstrated a strong antigen-specific recall challenge, and although not influenced by age, responsiveness to the recall challenge was associated with seroconversion. In older subjects, CMV seropositivity was associated with a significantly lower recall response to the vaccine, but the synbiotic did not affect the responsiveness of B or T cells to re-stimulation with influenza vaccine.
Conclusions: Antigen-specific B and T cell activation following an in vitro recall challenge with the influenza vaccine was influenced by CMV seropositivity, but not by a synbiotic.
Registered under ClinicalTrials.gov Identifier no. NCT01066377.
1-33
Enani, Sumaia
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Przemska-Kosicka, Agnieszka
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Childs, Caroline
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Maidens, Catherine
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Dong, Honglin
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Conterno, Lorenza
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Tuohy, Kieran
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Todd, Susan
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Gosney, Margot
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Yaqoob, Parveen
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Enani, Sumaia
c515f9bc-8172-462c-a080-07630ca74a41
Przemska-Kosicka, Agnieszka
5002ba00-920f-4772-8304-602b3ab9b570
Childs, Caroline
ea17ccc1-2eac-4f67-96c7-a0c4d9dfd9c5
Maidens, Catherine
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Dong, Honglin
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Conterno, Lorenza
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Tuohy, Kieran
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Todd, Susan
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Gosney, Margot
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Yaqoob, Parveen
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Enani, Sumaia, Przemska-Kosicka, Agnieszka, Childs, Caroline, Maidens, Catherine, Dong, Honglin, Conterno, Lorenza, Tuohy, Kieran, Todd, Susan, Gosney, Margot and Yaqoob, Parveen
(2017)
Impact of ageing and a synbiotic on the immune response to seasonal influenza vaccination; a randomised controlled trial.
Clinical Nutrition, .
(doi:10.1016/j.clnu.2017.01.011).
Abstract
Background & Aims: Ageing increases risk of respiratory infections and impairs the response to influenza vaccination. Pre- and probiotics offer an opportunity to modulate anti-viral defenses and the response to vaccination via alteration of the gut microbiota. This study investigated the effect of a novel probiotic, Bifidobacterium longum bv. infantis CCUG 52486, combined with a prebiotic, gluco-oligosaccharide, on the B and T cell response to seasonal influenza vaccination in young and older subjects.
Methods: In a double-blind, randomized controlled trial, 58 young (18-35y) and 54 older (60-85y) subjects were supplemented with the synbiotic for 8 weeks. At 4 weeks they were administered with a seasonal influenza vaccine. B and T cell phenotype and responsiveness to in vitro re-stimulation with the vaccine were assessed at baseline, 4, 6 and 8 weeks.
Results: B and T cell profiles differed markedly between young and older subjects. Vaccination increased numbers of memory, IgA+ memory, IgG+ memory and total IgG+ B cells in young subjects, but failed to do so in older subjects and did not significantly alter T cell subsets. Seroconversion to the H1N1 subunit in the older subjects was associated with higher post38 vaccination numbers of plasma B cells, but seroconversion was less consistently associated with T cell phenotype. B and T cell subsets from both young and older subjects demonstrated a strong antigen-specific recall challenge, and although not influenced by age, responsiveness to the recall challenge was associated with seroconversion. In older subjects, CMV seropositivity was associated with a significantly lower recall response to the vaccine, but the synbiotic did not affect the responsiveness of B or T cells to re-stimulation with influenza vaccine.
Conclusions: Antigen-specific B and T cell activation following an in vitro recall challenge with the influenza vaccine was influenced by CMV seropositivity, but not by a synbiotic.
Registered under ClinicalTrials.gov Identifier no. NCT01066377.
Text
Enani et al 2017 Accepted manuscript.pdf
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Accepted/In Press date: 20 January 2017
e-pub ahead of print date: 28 January 2017
Organisations:
Faculty of Medicine, Human Development & Health
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Local EPrints ID: 405261
URI: http://eprints.soton.ac.uk/id/eprint/405261
ISSN: 0261-5614
PURE UUID: cb79d881-15f9-4b43-a796-3754baa3e753
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Date deposited: 02 Feb 2017 10:18
Last modified: 16 Mar 2024 03:58
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Contributors
Author:
Sumaia Enani
Author:
Agnieszka Przemska-Kosicka
Author:
Catherine Maidens
Author:
Honglin Dong
Author:
Lorenza Conterno
Author:
Kieran Tuohy
Author:
Susan Todd
Author:
Margot Gosney
Author:
Parveen Yaqoob
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