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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...
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Published in: | Immunity, Inflammation and Disease Inflammation and Disease, 2023-06, Vol.11 (6), p.e867-n/a |
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creator | Moradi, Melika Vahedi, Farzaneh Abbassioun, Arian Ramezanpour Shahi, Arash Sholeh, Mohammad Taheri‐Anganeh, Mortaza Dargahi, Zahra Ghanavati, Roya Khatami, Seyyed Hossein Movahedpour, Ahmad |
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.
The delivery system and safety regulator are common characteristics of effective adjuvants in tuberculosis (TB) vaccines and the clinical trial stage. Based on our findings, the liposomal system is a superb adjuvant for vaccinations against TB, other intracellular infections, and malignancies. |
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The delivery system and safety regulator are common characteristics of effective adjuvants in tuberculosis (TB) vaccines and the clinical trial stage. Based on our findings, the liposomal system is a superb adjuvant for vaccinations against TB, other intracellular infections, and malignancies.</description><identifier>ISSN: 2050-4527</identifier><identifier>EISSN: 2050-4527</identifier><identifier>DOI: 10.1002/iid3.867</identifier><identifier>PMID: 37382263</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Adjuvants, Immunologic ; Antigens ; Bacterial infections ; Chemotherapy ; Clinical trials ; Drug resistance ; HIV ; Human immunodeficiency virus ; Humans ; Infections ; Infectious diseases ; Influenza ; Mortality ; Mycobacterium tuberculosis ; Proteins ; Review ; subunit vaccine ; Tuberculosis ; Tuberculosis Vaccines ; Tumor necrosis factor-TNF ; Vaccination ; Vaccines ; Viral infections</subject><ispartof>Immunity, Inflammation and Disease, 2023-06, Vol.11 (6), p.e867-n/a</ispartof><rights>2023 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd.</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5057-f8c13bc0bba62b9433e8955a65dbded9f6f5f9d75f8349b214be1d0dc4ea02723</citedby><cites>FETCH-LOGICAL-c5057-f8c13bc0bba62b9433e8955a65dbded9f6f5f9d75f8349b214be1d0dc4ea02723</cites><orcidid>0000-0002-0576-4435</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2830562521?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2830562521?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11561,25752,27923,27924,37011,37012,38515,43894,44589,46051,46475,53790,53792,74183,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37382263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moradi, Melika</creatorcontrib><creatorcontrib>Vahedi, Farzaneh</creatorcontrib><creatorcontrib>Abbassioun, Arian</creatorcontrib><creatorcontrib>Ramezanpour Shahi, Arash</creatorcontrib><creatorcontrib>Sholeh, Mohammad</creatorcontrib><creatorcontrib>Taheri‐Anganeh, Mortaza</creatorcontrib><creatorcontrib>Dargahi, Zahra</creatorcontrib><creatorcontrib>Ghanavati, Roya</creatorcontrib><creatorcontrib>Khatami, Seyyed Hossein</creatorcontrib><creatorcontrib>Movahedpour, Ahmad</creatorcontrib><title>Liposomal delivery system/adjuvant for tuberculosis vaccine</title><title>Immunity, Inflammation and Disease</title><addtitle>Immun Inflamm Dis</addtitle><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.
The delivery system and safety regulator are common characteristics of effective adjuvants in tuberculosis (TB) vaccines and the clinical trial stage. Based on our findings, the liposomal system is a superb adjuvant for vaccinations against TB, other intracellular infections, and malignancies.</description><subject>Adjuvants, Immunologic</subject><subject>Antigens</subject><subject>Bacterial infections</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Drug resistance</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Influenza</subject><subject>Mortality</subject><subject>Mycobacterium tuberculosis</subject><subject>Proteins</subject><subject>Review</subject><subject>subunit vaccine</subject><subject>Tuberculosis</subject><subject>Tuberculosis Vaccines</subject><subject>Tumor necrosis factor-TNF</subject><subject>Vaccination</subject><subject>Vaccines</subject><subject>Viral infections</subject><issn>2050-4527</issn><issn>2050-4527</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kV1rFDEUhoMottSCv0AGvPFm2nxMMgleiFRbFxa80euQj5OaJTNZk5kt---ddWttBa_O4ZyHh8N5EXpN8AXBmF7G6NmFFP0zdEoxx23Haf_8UX-CzmvdYIwJZj3D8iU6WaqkVLBT9H4dt7nmwaTGQ4o7KPum7usEw6Xxm3lnxqkJuTTTbKG4OeUaa7MzzsURXqEXwaQK5_f1DH2__vzt6ku7_nqzuvq4bh3HvG-DdIRZh601glrVMQZScW4E99aDV0EEHpTveZCsU5aSzgLx2LsODKY9ZWdodfT6bDZ6W-Jgyl5nE_XvQS632pQpugTa2Z5gDhyUYl1nlVHSOyGIZSFYZrrF9eHo2s52AO9gnIpJT6RPN2P8oW_zThNMOekFWwzv7g0l_5yhTnqI1UFKZoQ8V00lI1RJrsiCvv0H3eS5jMuvDhTmgnJK_gpdybUWCA_XEKwPCetDwnpJeEHfPL7-AfyT5wK0R-AuJtj_V6RXq0_sIPwFoOmvkA</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Moradi, Melika</creator><creator>Vahedi, Farzaneh</creator><creator>Abbassioun, Arian</creator><creator>Ramezanpour Shahi, Arash</creator><creator>Sholeh, Mohammad</creator><creator>Taheri‐Anganeh, Mortaza</creator><creator>Dargahi, Zahra</creator><creator>Ghanavati, Roya</creator><creator>Khatami, Seyyed Hossein</creator><creator>Movahedpour, Ahmad</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0576-4435</orcidid></search><sort><creationdate>202306</creationdate><title>Liposomal delivery system/adjuvant for tuberculosis vaccine</title><author>Moradi, Melika ; 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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.
The delivery system and safety regulator are common characteristics of effective adjuvants in tuberculosis (TB) vaccines and the clinical trial stage. Based on our findings, the liposomal system is a superb adjuvant for vaccinations against TB, other intracellular infections, and malignancies.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>37382263</pmid><doi>10.1002/iid3.867</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-0576-4435</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvants, Immunologic Antigens Bacterial infections Chemotherapy Clinical trials Drug resistance HIV Human immunodeficiency virus Humans Infections Infectious diseases Influenza Mortality Mycobacterium tuberculosis Proteins Review subunit vaccine Tuberculosis Tuberculosis Vaccines Tumor necrosis factor-TNF Vaccination Vaccines Viral infections |
title | Liposomal delivery system/adjuvant for tuberculosis vaccine |
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