Abstract

The importance of vaccine-induced protection was repeatedly demonstrated over the last three decades and emphasized during the recent COVID-19 pandemic as the safest and most effective way of preventing infectious diseases. Vaccines have controlled, and in some cases, eradicated global viral and bacterial infections with high efficiency and at a relatively low cost. Carbohydrates form the capsular sugar coat that surrounds the outer surface of human pathogenic bacteria. Specific surface-exposed bacterial carbohydrates serve as potent vaccine targets that broadened our toolbox against bacterial infections. Since first approved for commercial use, antibacterial carbohydrate-based vaccines mostly rely on inherently complex and heterogenous naturally derived polysaccharides, challenging to obtain in a pure, safe, and cost-effective manner. The introduction of synthetic fragments identical with bacterial capsular polysaccharides provided well-defined and homogenous structures that resolved many challenges of purified polysaccharides. The success of semisynthetic glycoconjugate vaccines against bacterial infections, now in different phases of clinical trials, opened up new possibilities and encouraged further development towards fully synthetic antibacterial vaccine solutions. In this mini-review, we describe the recent achievements in semi- and fully synthetic carbohydrate vaccines against a range of human pathogenic bacteria, focusing on preclinical and clinical studies.

Highlights

  • Over their 200-year history, vaccines have become the most cost-effective medical intervention to prevent morbidity and mortality worldwide

  • Aiming to improve Synflorix and Prevnar 13 by synthetic glycoconjugates, we proposed a pentavalent semisynthetic glycoconjugate pneumococcal vaccine that includes the following STs: (1) ST2, ST8, that have not been included in currently marketed vaccines, and ST3 absent from Synflorix; (2) ST5, which suffers from low immunogenicity or production inconsistencies; and (3) ST14 that is present in both licensed vaccines— it is included to show that nonproblematic STs from natural sources can be exchanged by synthetic glycoconjugates

  • A bivalent capsular polysaccharide (CPS)–ScpA193 vaccine conjugate composed of synthetic oligosaccharides from the repeating unit of the major and the conserved cell wall polysaccharide from Group A Streptococcus (GAS) STs conjugated to ScpA193, a novel streptococcal C5a peptidase (ScpA) mutant as the protein carrier

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Summary

Introduction

Over their 200-year history, vaccines have become the most cost-effective medical intervention to prevent morbidity and mortality worldwide. A comparative immunological study of synthetic oligosaccharides of the CPS repeating units of ST3 [37] and ST14 [38,39] conjugated to bovine serum albumin (BSA) revealed that the optimal candidates for semisynthetic vaccines for both STs are tetrasaccharide ligands.

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