Literature DB >> 34972938

Glycan Microarrays Containing Synthetic Streptococcus pneumoniae CPS Fragments and Their Application to Vaccine Development.

Paulina Kaplonek1,2, Peter H Seeberger3,4.   

Abstract

Streptococcus pneumoniae is the leading source of life-endangering diseases like pneumonia, septicemia, and meningitis, as well as a major cause of death in children under 5 years old in developing countries. At least 98 serotypes of S. pneumoniae can be distinguished based on their structurally distinct capsular polysaccharides (CPS). Currently available CPS-based pneumococcal vaccines contain serotypes most frequently associated with invasive pneumococcal diseases. The polysaccharides used in commercial conjugate-vaccines are isolated from bacteria cultures comprising many laborious and operationally challenging steps followed by depolymerization of long polysaccharides into small fragments and their conjugation to the carrier protein. The medicinal chemistry approach for glycoconjugate vaccine development offers an exciting alternative to CPS isolation for a broad range of different glycan antigens. Glycan arrays containing well-defined synthetic glycans of CPS fragments and repeating units are used as a platform for the high-throughput screening of various serum samples and identification of protective glycotopes for vaccine candidates.
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Bacterial polysaccharides; Microbial glycans; Oligosaccharide microarrays; Polysaccharide fragments; Streptococcus pneumonia; Vaccines

Mesh:

Substances:

Year:  2022        PMID: 34972938     DOI: 10.1007/978-1-0716-2148-6_12

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  27 in total

Review 1.  Community-acquired pneumonia as an emergency condition.

Authors:  Catia Cillóniz; Cristina Dominedò; Carolina Garcia-Vidal; Antoni Torres
Journal:  Curr Opin Crit Care       Date:  2018-12       Impact factor: 3.687

Review 2.  Structural analysis of glucans.

Authors:  Andriy Synytsya; Miroslav Novak
Journal:  Ann Transl Med       Date:  2014-02

3.  Herd immunity and serotype replacement 4 years after seven-valent pneumococcal conjugate vaccination in England and Wales: an observational cohort study.

Authors:  Elizabeth Miller; Nicholas J Andrews; Pauline A Waight; Mary Pe Slack; Robert C George
Journal:  Lancet Infect Dis       Date:  2011-05-27       Impact factor: 25.071

Review 4.  Pneumococcal Capsules and Their Types: Past, Present, and Future.

Authors:  K Aaron Geno; Gwendolyn L Gilbert; Joon Young Song; Ian C Skovsted; Keith P Klugman; Christopher Jones; Helle B Konradsen; Moon H Nahm
Journal:  Clin Microbiol Rev       Date:  2015-07       Impact factor: 26.132

Review 5.  Development and clinical evaluation of Prevnar 13, a 13-valent pneumocococcal CRM197 conjugate vaccine.

Authors:  William C Gruber; Daniel A Scott; Emilio A Emini
Journal:  Ann N Y Acad Sci       Date:  2012-07-25       Impact factor: 5.691

6.  Surface charge of Streptococcus pneumoniae predicts serotype distribution.

Authors:  Yuan Li; Daniel M Weinberger; Claudette M Thompson; Krzysztof Trzciński; Marc Lipsitch
Journal:  Infect Immun       Date:  2013-09-30       Impact factor: 3.441

Review 7.  Development of pneumococcal vaccines over the last 10 years.

Authors:  Nicola Principi; Susanna Esposito
Journal:  Expert Opin Biol Ther       Date:  2017-10-12       Impact factor: 4.388

Review 8.  Community-Acquired Pneumonia in Children: the Challenges of Microbiological Diagnosis.

Authors:  C M C Rodrigues; H Groves
Journal:  J Clin Microbiol       Date:  2018-02-22       Impact factor: 5.948

9.  Automated Glycan Assembly: A Perspective.

Authors:  Mónica Guberman; Peter H Seeberger
Journal:  J Am Chem Soc       Date:  2019-03-28       Impact factor: 15.419

Review 10.  Neonatal and infantile immune responses to encapsulated bacteria and conjugate vaccines.

Authors:  Peter Klein Klouwenberg; Louis Bont
Journal:  Clin Dev Immunol       Date:  2008
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