Chemoenzymatic synthesis of arabinomannan (AM) glycoconjugates as potential vaccines for tuberculosis.


Journal

European journal of medicinal chemistry
ISSN: 1768-3254
Titre abrégé: Eur J Med Chem
Pays: France
ID NLM: 0420510

Informations de publication

Date de publication:
15 Oct 2020
Historique:
received: 06 05 2020
revised: 11 06 2020
accepted: 12 06 2020
pubmed: 28 7 2020
medline: 20 4 2021
entrez: 28 7 2020
Statut: ppublish

Résumé

Mycobacteria infection resulting in tuberculosis (TB) is one of the top ten leading causes of death worldwide in 2018, and lipoarabinomannan (LAM) has been confirmed to be the most important antigenic polysaccharide on the TB cell surface. In this study, a convenient synthetic method has been developed for synthesizing three branched oligosaccharides derived from LAM, in which a core building block was prepared by enzymatic hydrolysis in flow chemistry with excellent yield. After several steps of glycosylations, the obtained oligosaccharides were conjugated with recombinant human serum albumin (rHSA) and the ex-vivo ELISA tests were performed using serum obtained from several TB-infected patients, in order to evaluate the affinity of the glycoconjugate products for the human LAM-antibodies. The evaluation results are positive, especially compound 21 that exhibited excellent activity which could be considered as a lead compound for the future development of a new glycoconjugated vaccine against TB.

Identifiants

pubmed: 32717482
pii: S0223-5234(20)30550-X
doi: 10.1016/j.ejmech.2020.112578
pii:
doi:

Substances chimiques

Bacterial Vaccines 0
Glycoconjugates 0
Mannans 0
arabinomannan 53026-40-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

112578

Informations de copyright

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Zhihao Li (Z)

Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, UMR 8232, 4 Place Jussieu, 75005, Paris, France.

Teodora Bavaro (T)

Drug Sciences Department, University of Pavia, Viale Taramelli 12, 27100, Pavia, Italy.

Sara Tengattini (S)

Drug Sciences Department, University of Pavia, Viale Taramelli 12, 27100, Pavia, Italy.

Roberta Bernardini (R)

Italy Centro Servizi Interdipartimentale - STA, University of Rome "Tor Vergata", Rome, Italy.

Maurizio Mattei (M)

Italy Centro Servizi Interdipartimentale - STA, University of Rome "Tor Vergata", Rome, Italy; Department of Biology, University of Rome "Tor Vergata", Rome, Italy.

Francesca Annunziata (F)

Department of Pharmaceutical Sciences, University of Milan, via Mangiagalli 25, 20133, Milan, Italy.

Richard B Cole (RB)

Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, UMR 8232, 4 Place Jussieu, 75005, Paris, France.

Changping Zheng (C)

Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, UMR 8232, 4 Place Jussieu, 75005, Paris, France.

Matthieu Sollogoub (M)

Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, UMR 8232, 4 Place Jussieu, 75005, Paris, France.

Lucia Tamborini (L)

Department of Pharmaceutical Sciences, University of Milan, via Mangiagalli 25, 20133, Milan, Italy.

Marco Terreni (M)

Drug Sciences Department, University of Pavia, Viale Taramelli 12, 27100, Pavia, Italy. Electronic address: marco.terreni@unipv.it.

Yongmin Zhang (Y)

Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, UMR 8232, 4 Place Jussieu, 75005, Paris, France; Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education, College of Chemistry & Chemical Engineering, Hainan Normal University, Haikou 571158, China. Electronic address: yongmin.zhang@upmc.fr.

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Classifications MeSH