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PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine
The available HBV vaccines based on the HBV surface protein are manufactured in yeasts and demonstrate excellent prophylactic but no therapeutic activity and are thus ineffective against chronic HBV infection. Five different HBV core proteins (HBc)—full length and C-terminally truncated—were used fo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142831/ https://www.ncbi.nlm.nih.gov/pubmed/37110395 http://dx.doi.org/10.3390/microorganisms11040972 |
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author | Dishlers, Andris Petrovskis, Ivars Skrastina, Dace Zarina, Ieva Lieknina, Ilva Jansons, Juris Akopjana, Inara Zakova, Jelena Ose, Velta Sominskaya, Irina |
author_facet | Dishlers, Andris Petrovskis, Ivars Skrastina, Dace Zarina, Ieva Lieknina, Ilva Jansons, Juris Akopjana, Inara Zakova, Jelena Ose, Velta Sominskaya, Irina |
author_sort | Dishlers, Andris |
collection | PubMed |
description | The available HBV vaccines based on the HBV surface protein are manufactured in yeasts and demonstrate excellent prophylactic but no therapeutic activity and are thus ineffective against chronic HBV infection. Five different HBV core proteins (HBc)—full length and C-terminally truncated—were used for the insertion of the short, preS1,aa 20–47 and long, preS1phil, aa 12–60 + 89–119 fragments. Modified virus-like particles (VLPs) were compared for their biotechnological and immunological properties. The expression level of HBc-preS1 proteins was high for all investigated proteins, allowing us to obtain 10–20 mg of purified VLPs from a gram of biomass with the combination of gel filtration and ion-exchange chromatography to reach approximately 90% purity of target proteins. The immunogenicity of chimeric VLPs was tested in BALB/c mice, showing a high anti-preS1 response and substantial T-cell proliferation after stimulation with HBc protein. Targeted incorporation of oligonucleotide ODN 1668 in modified HBc-preS1 VLPs was demonstrated. |
format | Online Article Text |
id | pubmed-10142831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101428312023-04-29 PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine Dishlers, Andris Petrovskis, Ivars Skrastina, Dace Zarina, Ieva Lieknina, Ilva Jansons, Juris Akopjana, Inara Zakova, Jelena Ose, Velta Sominskaya, Irina Microorganisms Article The available HBV vaccines based on the HBV surface protein are manufactured in yeasts and demonstrate excellent prophylactic but no therapeutic activity and are thus ineffective against chronic HBV infection. Five different HBV core proteins (HBc)—full length and C-terminally truncated—were used for the insertion of the short, preS1,aa 20–47 and long, preS1phil, aa 12–60 + 89–119 fragments. Modified virus-like particles (VLPs) were compared for their biotechnological and immunological properties. The expression level of HBc-preS1 proteins was high for all investigated proteins, allowing us to obtain 10–20 mg of purified VLPs from a gram of biomass with the combination of gel filtration and ion-exchange chromatography to reach approximately 90% purity of target proteins. The immunogenicity of chimeric VLPs was tested in BALB/c mice, showing a high anti-preS1 response and substantial T-cell proliferation after stimulation with HBc protein. Targeted incorporation of oligonucleotide ODN 1668 in modified HBc-preS1 VLPs was demonstrated. MDPI 2023-04-08 /pmc/articles/PMC10142831/ /pubmed/37110395 http://dx.doi.org/10.3390/microorganisms11040972 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dishlers, Andris Petrovskis, Ivars Skrastina, Dace Zarina, Ieva Lieknina, Ilva Jansons, Juris Akopjana, Inara Zakova, Jelena Ose, Velta Sominskaya, Irina PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine |
title | PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine |
title_full | PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine |
title_fullStr | PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine |
title_full_unstemmed | PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine |
title_short | PreS1 Containing HBc VLPs for the Development of a Combined Therapeutic/Prophylactic Hepatitis B Vaccine |
title_sort | pres1 containing hbc vlps for the development of a combined therapeutic/prophylactic hepatitis b vaccine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142831/ https://www.ncbi.nlm.nih.gov/pubmed/37110395 http://dx.doi.org/10.3390/microorganisms11040972 |
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