Catherine Guerreiro

CNRS UMR3523, 28 Rue Du Dr Roux, 75724 Paris Cedex 15
Paris, 75724, France

Last Updated: 09/26/2026

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Found 8 publications

The First-in-Human Synthetic Glycan-Based Conjugate Vaccine Candidate against Shigella.

The First-in-Human Synthetic Glycan-Based Conjugate Vaccine Candidate against Shigella.

Journal: ACS central science

Published: December 01, 2021

Dirhamnolipids secreted from Pseudomonas aeruginosa modify anjpegungal susceptibility of Aspergillus fumigatus by inhibiting β1,3 glucan synthase activity.

Dirhamnolipids secreted from Pseudomonas aeruginosa modify anjpegungal susceptibility of Aspergillus fumigatus by inhibiting β1,3 glucan synthase activity.

Journal: The ISME journal

Published: November 03, 2016

A Synthetic Carbohydrate Conjugate Vaccine Candidate against Shigellosis: Improved Bioconjugation and Impact of Alum on Immunogenicity.

A Synthetic Carbohydrate Conjugate Vaccine Candidate against Shigellosis: Improved Bioconjugation and Impact of Alum on Immunogenicity.

Journal: Bioconjugate chemistry

Published: February 27, 2016

Detailed Investigation of the Immunodominant Role of O-Antigen Stoichiometric O-Acetylation as Revealed by Chemical Synthesis, Immunochemistry, Solution Conformation and STD-NMR Spectroscopy for Shigella flexneri 3a.

Detailed Investigation of the Immunodominant Role of O-Antigen Stoichiometric O-Acetylation as Revealed by Chemical Synthesis, Immunochemistry, Solution Conformation and STD-NMR Spectroscopy for Shigella flexneri 3a.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: February 05, 2016

Programmed chemo-enzymatic synthesis of the oligosaccharide component of a carbohydrate-based antibacterial vaccine candidate.

Programmed chemo-enzymatic synthesis of the oligosaccharide component of a carbohydrate-based antibacterial vaccine candidate.

Journal: Chemical communications (Cambridge, England)

Published: January 09, 2015

Linear synthesis of the branched pentasaccharide repeats of O-antigens from Shigella flexneri 1a and 1b demonstrating the major steric hindrance associated with type-specific glucosylation.

Linear synthesis of the branched pentasaccharide repeats of O-antigens from Shigella flexneri 1a and 1b demonstrating the major steric hindrance associated with type-specific glucosylation.

Journal: Organic & biomolecular chemistry

Published: August 22, 2014

Non-stoichiometric O-acetylation of Shigella flexneri 2a O-specific polysaccharide: synthesis and antigenicity.

Non-stoichiometric O-acetylation of Shigella flexneri 2a O-specific polysaccharide: synthesis and antigenicity.

Journal: Organic & biomolecular chemistry

Published: May 20, 2014

CGTase-catalysed cis-glucosylation of L-rhamnosides for the preparation of Shigella flexneri 2a and 3a haptens.

CGTase-catalysed cis-glucosylation of L-rhamnosides for the preparation of Shigella flexneri 2a and 3a haptens.

Journal: Chembiochem : a European journal of chemical biology

Published: September 16, 2013

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Last Updated: 09/26/2026