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Liposomal delivery system/adjuvant for tuberculosis vaccine
As reported by the World Health Organization, about 10 million individuals were infected with tuberculosis (TB) worldwide. Moreover, approximately 1.5 million people died of TB, of which 214,000 were infected with HIV simultaneously. Due to the high infection rate, the need for effective TB vaccinat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10251763/ https://www.ncbi.nlm.nih.gov/pubmed/37382263 http://dx.doi.org/10.1002/iid3.867 |
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author | Moradi, Melika Vahedi, Farzaneh Abbassioun, Arian Ramezanpour Shahi, Arash Sholeh, Mohammad Taheri‐Anganeh, Mortaza Dargahi, Zahra Ghanavati, Roya Khatami, Seyyed Hossein Movahedpour, Ahmad |
author_facet | Moradi, Melika Vahedi, Farzaneh Abbassioun, Arian Ramezanpour Shahi, Arash Sholeh, Mohammad Taheri‐Anganeh, Mortaza Dargahi, Zahra Ghanavati, Roya Khatami, Seyyed Hossein Movahedpour, Ahmad |
author_sort | Moradi, Melika |
collection | PubMed |
description | As reported by the World Health Organization, about 10 million individuals were infected with tuberculosis (TB) worldwide. Moreover, approximately 1.5 million people died of TB, of which 214,000 were infected with HIV simultaneously. Due to the high infection rate, the need for effective TB vaccination is highly felt. Until now, various methodologies have been proposed for the development of a protein subunit vaccine for TB. These vaccines have shown higher protection than other vaccines, particularly the Bacillus culture vaccine. The delivery system and safety regulator are common characteristics of effective adjuvants in TB vaccines and the clinical trial stage. The present study investigates the current state of TB adjuvant research focusing on the liposomal adjuvant system. Based on our findings, the liposomal system is a safe and efficient adjuvant from nanosize to microsize for vaccinations against TB, other intracellular infections, and malignancies. Clinical studies can provide valuable feedback for developing novel TB adjuvants, which ultimately enhance the impact of adjuvants on next‐generation TB vaccines. |
format | Online Article Text |
id | pubmed-10251763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102517632023-06-10 Liposomal delivery system/adjuvant for tuberculosis vaccine Moradi, Melika Vahedi, Farzaneh Abbassioun, Arian Ramezanpour Shahi, Arash Sholeh, Mohammad Taheri‐Anganeh, Mortaza Dargahi, Zahra Ghanavati, Roya Khatami, Seyyed Hossein Movahedpour, Ahmad Immun Inflamm Dis Review Articles As reported by the World Health Organization, about 10 million individuals were infected with tuberculosis (TB) worldwide. Moreover, approximately 1.5 million people died of TB, of which 214,000 were infected with HIV simultaneously. Due to the high infection rate, the need for effective TB vaccination is highly felt. Until now, various methodologies have been proposed for the development of a protein subunit vaccine for TB. These vaccines have shown higher protection than other vaccines, particularly the Bacillus culture vaccine. The delivery system and safety regulator are common characteristics of effective adjuvants in TB vaccines and the clinical trial stage. The present study investigates the current state of TB adjuvant research focusing on the liposomal adjuvant system. Based on our findings, the liposomal system is a safe and efficient adjuvant from nanosize to microsize for vaccinations against TB, other intracellular infections, and malignancies. Clinical studies can provide valuable feedback for developing novel TB adjuvants, which ultimately enhance the impact of adjuvants on next‐generation TB vaccines. John Wiley and Sons Inc. 2023-06-09 /pmc/articles/PMC10251763/ /pubmed/37382263 http://dx.doi.org/10.1002/iid3.867 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Articles Moradi, Melika Vahedi, Farzaneh Abbassioun, Arian Ramezanpour Shahi, Arash Sholeh, Mohammad Taheri‐Anganeh, Mortaza Dargahi, Zahra Ghanavati, Roya Khatami, Seyyed Hossein Movahedpour, Ahmad Liposomal delivery system/adjuvant for tuberculosis vaccine |
title | Liposomal delivery system/adjuvant for tuberculosis vaccine |
title_full | Liposomal delivery system/adjuvant for tuberculosis vaccine |
title_fullStr | Liposomal delivery system/adjuvant for tuberculosis vaccine |
title_full_unstemmed | Liposomal delivery system/adjuvant for tuberculosis vaccine |
title_short | Liposomal delivery system/adjuvant for tuberculosis vaccine |
title_sort | liposomal delivery system/adjuvant for tuberculosis vaccine |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10251763/ https://www.ncbi.nlm.nih.gov/pubmed/37382263 http://dx.doi.org/10.1002/iid3.867 |
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