Abstract

Recently, generalized modules for membrane antigens (GMMA) technology has been proposed as an alternative approach to traditional glycoconjugate vaccines for O-antigen delivery. Saccharide length is a well-known parameter that can impact the immune response induced by glycoconjugates both in terms of magnitude and quality. However, the criticality of O-antigen length on the immune response induced by GMMA-based vaccines has not been fully elucidated. Here, Shigella and Salmonella GMMA-producing strains were further mutated in order to display homogeneous polysaccharide populations of different sizes on a GMMA surface. Resulting GMMA were compared in mice immunization studies. Athymic nude mice were also used to investigate the involvement of T-cells in the immune response elicited. In contrast with what has been reported for traditional glycoconjugate vaccines and independent of the pathogen and the sugar structural characteristics, O-antigen length did not result in being a critical parameter for GMMA immunogenicity. This work supports the identification of critical quality attributes to optimize GMMA vaccine design and improve vaccine efficacy and gives insights on the nature of the immune response induced by GMMA.

Highlights

  • Published: 28 January 2021The O-antigen (OAg) moiety of lipopolysaccharide (LPS) has been recognized as a key target for protective immunity against several pathogens, including Shigella species and non-typhoidal Salmonellae (NTS) [1,2]

  • The phenotype resulting from each mutation was analyzed by a silver-staining analysis of LPS extracted from bacterial cells and high-performance liquid chromatography–size exclusion chromatography (HPLC–SEC)

  • generalized modules for membrane antigens (GMMA) can be characterized by very different OAg lengths as a result of pathogen-specific biosynthetic pathways leading to the expression of heterogeneous polysaccharide species with different degrees of polymerization

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Summary

Introduction

The O-antigen (OAg) moiety of lipopolysaccharide (LPS) has been recognized as a key target for protective immunity against several pathogens, including Shigella species and non-typhoidal Salmonellae (NTS) [1,2]. Generalized modules for membrane antigens (GMMA) technology has been proposed as an alternative approach to traditional glycoconjugate vaccines for OAg delivery [3]. GMMA display the OAg in an outer membrane context and have been proven to be non-inferior compared to equivalent glycoconjugate vaccines in preclinical studies [6,7]. OAg length is well known to be a parameter that can impact the immune response induced [9]. Shigella sonnei conjugates with low molecular-mass OAg fragments (average of 3.5 repeating units) induced significantly higher antibody levels in mice than the full-length OAg

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