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Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes

BACKGROUND: There is an urgent need to develop safe and effective adjuvants for the new generation of subunit vaccines. We developed the tubular immunostimulating complex (TI-complex) as a new nanoparticulate antigen delivery system. The morphology and composition of TI-complexes principally differ...

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Autores principales: Kostetsky, Eduard Y, Sanina, Nina M, Mazeika, Andrey N, Tsybulsky, Alexander V, Vorobyeva, Natalia S, Shnyrov, Valery L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175152/
https://www.ncbi.nlm.nih.gov/pubmed/21888630
http://dx.doi.org/10.1186/1477-3155-9-35
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author Kostetsky, Eduard Y
Sanina, Nina M
Mazeika, Andrey N
Tsybulsky, Alexander V
Vorobyeva, Natalia S
Shnyrov, Valery L
author_facet Kostetsky, Eduard Y
Sanina, Nina M
Mazeika, Andrey N
Tsybulsky, Alexander V
Vorobyeva, Natalia S
Shnyrov, Valery L
author_sort Kostetsky, Eduard Y
collection PubMed
description BACKGROUND: There is an urgent need to develop safe and effective adjuvants for the new generation of subunit vaccines. We developed the tubular immunostimulating complex (TI-complex) as a new nanoparticulate antigen delivery system. The morphology and composition of TI-complexes principally differ from the known vesicular immunostimulating complexes (ISCOMs). However, methodology for the preparation of TI-complexes has suffered a number of shortcomings. The aim of the present work was to obtain an antigen carrier consisting of triterpene glycosides from Cucumaria japonica, cholesterol, and monogalactosyldiacylglycerol from marine macrophytes with reproducible properties and high adjuvant activity. RESULTS: The cucumarioside A(2)-2 - cholesterol - MGalDG ratio of 6:2:4 (by weight) was found to provide the most effective formation of TI-complexes and the minimum hemolytic activity in vitro. Tubules of TI-complexes have an outer diameter of about 16 nm, an inner diameter of 6 nm, and a length of 500 nm. A significant dilution by the buffer gradually destroyed the tubular nanoparticles. The TI-complex was able to increase the immunogenicity of the protein antigens from Yersinia pseudotuberculosis by three to four times. CONCLUSIONS: We propose an optimized methodology for the preparation of homogeneous TI-complexes containing only tubular particles, which would achieve reproducible immunization results. We suggest that the elaborated TI-complexes apply as a universal delivery system for different subunit antigens within anti-infectious vaccines and enhance their economic efficacy and safety.
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spelling pubmed-31751522011-09-18 Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes Kostetsky, Eduard Y Sanina, Nina M Mazeika, Andrey N Tsybulsky, Alexander V Vorobyeva, Natalia S Shnyrov, Valery L J Nanobiotechnology Research BACKGROUND: There is an urgent need to develop safe and effective adjuvants for the new generation of subunit vaccines. We developed the tubular immunostimulating complex (TI-complex) as a new nanoparticulate antigen delivery system. The morphology and composition of TI-complexes principally differ from the known vesicular immunostimulating complexes (ISCOMs). However, methodology for the preparation of TI-complexes has suffered a number of shortcomings. The aim of the present work was to obtain an antigen carrier consisting of triterpene glycosides from Cucumaria japonica, cholesterol, and monogalactosyldiacylglycerol from marine macrophytes with reproducible properties and high adjuvant activity. RESULTS: The cucumarioside A(2)-2 - cholesterol - MGalDG ratio of 6:2:4 (by weight) was found to provide the most effective formation of TI-complexes and the minimum hemolytic activity in vitro. Tubules of TI-complexes have an outer diameter of about 16 nm, an inner diameter of 6 nm, and a length of 500 nm. A significant dilution by the buffer gradually destroyed the tubular nanoparticles. The TI-complex was able to increase the immunogenicity of the protein antigens from Yersinia pseudotuberculosis by three to four times. CONCLUSIONS: We propose an optimized methodology for the preparation of homogeneous TI-complexes containing only tubular particles, which would achieve reproducible immunization results. We suggest that the elaborated TI-complexes apply as a universal delivery system for different subunit antigens within anti-infectious vaccines and enhance their economic efficacy and safety. BioMed Central 2011-09-02 /pmc/articles/PMC3175152/ /pubmed/21888630 http://dx.doi.org/10.1186/1477-3155-9-35 Text en Copyright ©2011 Kostetsky et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kostetsky, Eduard Y
Sanina, Nina M
Mazeika, Andrey N
Tsybulsky, Alexander V
Vorobyeva, Natalia S
Shnyrov, Valery L
Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes
title Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes
title_full Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes
title_fullStr Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes
title_full_unstemmed Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes
title_short Tubular immunostimulating complex based on cucumarioside A(2)-2 and monogalactosyldiacylglycerol from marine macrophytes
title_sort tubular immunostimulating complex based on cucumarioside a(2)-2 and monogalactosyldiacylglycerol from marine macrophytes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175152/
https://www.ncbi.nlm.nih.gov/pubmed/21888630
http://dx.doi.org/10.1186/1477-3155-9-35
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