CONFERENCE PROCEEDING
Synthesis of third-generation carbohydrate vaccines against fungal and bacterial pathogens
 
More details
Hide details
1
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia
 
 
Publication date: 2024-04-16
 
 
Corresponding author
Vadim B. Krylov
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect 47, 119991 Moscow, Russia
 
 
Public Health Toxicol 2024;4(Supplement Supplement 1):A15
 
KEYWORDS
ABSTRACT
Antigenic polysaccharides present on the surface of the cell wall of myco- and bacterial pathogens play an important role at various stages of their biological recognition. In this regard, synthetic oligosaccharide ligands, structurally related to the polysaccharides of the cell wall of infectious agents, are a convenient basis for the development of specific vaccines and diagnostics for pathogen detection and control of vaccination efficiency [1,2]. This report discusses the main stages in the development of 3rd generation carbohydrate vaccines (synthetic conjugate vaccines). The original methods of stereospecific synthesis of oligosaccharides developed in our laboratory made it possible to obtain preparative amounts of oligosaccharide ligands corresponding to immunodeterminant fragments of bacterial and fungal antigens. Thus, using the pyranoside-into-furanoside rearrangement discovered by our team [3], we obtained oligosaccharides related to polysaccharides of bacteria (Klebsiella pneumonia [4,5], Enterococcus faecalis [6]), as well as fungal pathogens (Aspergillus fumigatus [7-9]). The resulting oligosaccharides allow of detailed characterization of the carbohydrate specificity of antibodies against pathogens [10,11], and then create conjugated candidate vaccines that make it possible to induce protective antibodies that prevent infections [6], including those caused by antibiotic-resistant strains of hospital infections.

Conflicts of Interest:
The authors declare that they have no conflict of interest in the publication of this article. The authors have no conflicts of interest to report in this work. Abstract was not submitted elsewhere and published here firstly.

Funding:
This work was supported by the Ministry of Science and Higher Education of the Russian Federation (Theme No. FFZZ-2022-0010) for new laboratories in the direction of "New Medicine"

 
REFERENCES (11)
1.
V. B. Krylov and N. E. Nifantiev, Curr. Top. Microbiol. Immunol., 2020, 425, 1–16.
 
2.
V. B. Krylov and N. E. Nifantiev, Drug Discov. Today Technol., 2020, 35–36, 35–43.
 
3.
V. B. Krylov, D. A. Argunov, D. Z. Vinnitskiy, S. A. Verkhnyatskaya, A. G. Gerbst, N. E. Ustyuzhanina, A. S. Dmitrenok, J. Huebner, O. Holst, H.-C. Siebert and N. E. Nifantiev, Chem. Eur. J., 2014, 20, 16516–16522.
 
4.
S. A. Verkhnyatskaya, V. B. Krylov and N. E. Nifantiev, Eur. J. Org. Chem., 2017, 2017, 710–718.
 
5.
D. A. Argunov, A. S. Trostianetskaia, V. B. Krylov, E. A. Kurbatova and N. E. Nifantiev, Eur. J. Org. Chem., 2019, 2019, 4226–4232.
 
6.
D. Laverde, F. Romero-Saavedra, D. A. Argunov, J. Enotarpi, V. B. Krylov, E. Kalfopoulou, C. Martini, R. Torelli, G. A. van der Marel, M. Sanguinetti, J. D. C. Codée, N. E. Nifantiev and J. Huebner, ACS Infect. Dis., 2020, 6, 1816–1826.
 
7.
D. A. Argunov, V. B. Krylov and N. E. Nifantiev, Org. Biomol. Chem., 2015, 13, 3255–3267.
 
8.
D. A. Argunov, V. B. Krylov and N. E. Nifantiev, Org. Lett., 2016, 18, 5504–5507.
 
9.
V. B. Krylov, D. A. Argunov, A. S. Solovev, M. I. Petruk, A. G. Gerbst, A. S. Dmitrenok, A. S. Shashkov, J.-P. Latgé and N. E. Nifantiev, Org. Biomol. Chem., 2018, 16, 1188–1199.
 
10.
V. B. Krylov, A. S. Solovev, I. A. Puchkin, D. V. Yashunsky, A. V. Antonets, O. Y. Kutsevalova and N. E. Nifantiev, J. Fungi, 2021, 7, 504.
 
11.
S. S. W. Wong, V. B. Krylov, D. A. Argunov, A. A. Karelin, J.-P. Bouchara, T. Fontaine, J.-P. Latgé and N. E. Nifantiev, mSphere, 2020, 5, e00688-19.
 
ISSN:2732-8929
Journals System - logo
Scroll to top