Strategies in the design and use of synthetic "internal glycan" vaccines

The relative structural conservation of "internal glycans" in the cell walls of pathogens suggests that they might as target epitopes less prone to variation and hence with greater potential universality as vaccine targets. Examples of such glycans include the inner core sugars of lipopoly...

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Main Authors: Lakshminarayanan, A, Vijayakrishnan, B, Bayley, H, Davis, B
Format: Book section
Language:English
Published: Elsevier 2017
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author Lakshminarayanan, A
Vijayakrishnan, B
Bayley, H
Davis, B
author_facet Lakshminarayanan, A
Vijayakrishnan, B
Bayley, H
Davis, B
author_sort Lakshminarayanan, A
collection OXFORD
description The relative structural conservation of "internal glycans" in the cell walls of pathogens suggests that they might as target epitopes less prone to variation and hence with greater potential universality as vaccine targets. Examples of such glycans include the inner core sugars of lipopolysaccharides in Gram-negative bacteria. However, due to the buried nature of such internal epitopes, this approach has been rarely adopted. Here we briefly review and compare strategic approaches and outline practical methods associated with evaluating one synergistic strategy that combines (i) blocking of the display of "external glycans" with (ii) vaccination targeted at "internal glycans."
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spelling oxford-uuid:5b6f4aa5-e19a-4360-b011-f28f702f93282022-03-26T17:22:02ZStrategies in the design and use of synthetic "internal glycan" vaccinesBook sectionhttp://purl.org/coar/resource_type/c_3248uuid:5b6f4aa5-e19a-4360-b011-f28f702f9328EnglishSymplectic Elements at OxfordElsevier2017Lakshminarayanan, AVijayakrishnan, BBayley, HDavis, BThe relative structural conservation of "internal glycans" in the cell walls of pathogens suggests that they might as target epitopes less prone to variation and hence with greater potential universality as vaccine targets. Examples of such glycans include the inner core sugars of lipopolysaccharides in Gram-negative bacteria. However, due to the buried nature of such internal epitopes, this approach has been rarely adopted. Here we briefly review and compare strategic approaches and outline practical methods associated with evaluating one synergistic strategy that combines (i) blocking of the display of "external glycans" with (ii) vaccination targeted at "internal glycans."
spellingShingle Lakshminarayanan, A
Vijayakrishnan, B
Bayley, H
Davis, B
Strategies in the design and use of synthetic "internal glycan" vaccines
title Strategies in the design and use of synthetic "internal glycan" vaccines
title_full Strategies in the design and use of synthetic "internal glycan" vaccines
title_fullStr Strategies in the design and use of synthetic "internal glycan" vaccines
title_full_unstemmed Strategies in the design and use of synthetic "internal glycan" vaccines
title_short Strategies in the design and use of synthetic "internal glycan" vaccines
title_sort strategies in the design and use of synthetic internal glycan vaccines
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