Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccines

The threat of influenza A virus (IAV) remains an annual health concern, as almost 500,000 people die each year due to the seasonal flu. Current flu vaccines are highly dependent on embryonated chicken eggs for production, which is time consuming and costly. These vaccines only confer moderate protec...

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Main Authors: Jaffar Ali Muhamad Norizwan, Wen Siang Tan
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Current Research in Microbial Sciences
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Online Access:http://www.sciencedirect.com/science/article/pii/S2666517424001007
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author Jaffar Ali Muhamad Norizwan
Wen Siang Tan
author_facet Jaffar Ali Muhamad Norizwan
Wen Siang Tan
author_sort Jaffar Ali Muhamad Norizwan
collection DOAJ
description The threat of influenza A virus (IAV) remains an annual health concern, as almost 500,000 people die each year due to the seasonal flu. Current flu vaccines are highly dependent on embryonated chicken eggs for production, which is time consuming and costly. These vaccines only confer moderate protections in elderly people, and they lack cross-protectivity; thereby requiring annual reformulation to ensure effectiveness against contemporary circulating strains. To address current limitations, new strategies are being sought, with great emphasis given on exploiting IAV's conserved antigens for vaccine development, and by using different vaccine technologies to enhance immunogenicity and expedite vaccine production. Among these technologies, there are growing pre-clinical and clinical studies involving virus-like particles (VLPs), as they are capable to display multiple conserved IAV antigens and augment their immune responses. In this review, we outline recent findings involving broadly effective IAV antigens and strategies to display these antigens on VLPs. Current production systems for IAV VLP vaccines are comprehensively reviewed. Pain-free methods for administration of IAV VLP vaccines through intranasal and transdermal routes, as well as the mechanisms in stimulating immune responses are discussed in detail. The future perspectives of VLPs in IAV vaccine development are discussed, particularly concerning their potentials in overcoming current immunological limitations of IAV vaccines, and their inherent advantages in exploring intranasal vaccination studies. We also propose avenues to expedite VLP vaccine production, as we envision that there will be more clinical trials involving IAV VLP vaccines, leading to commercialization of these vaccines in the near future.
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spelling doaj-art-929a171c05a745cb84f4d8218f94ab6c2025-08-20T02:35:44ZengElsevierCurrent Research in Microbial Sciences2666-51742025-01-01810031710.1016/j.crmicr.2024.100317Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccinesJaffar Ali Muhamad Norizwan0Wen Siang Tan1Department of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, MalaysiaCorresponding author.; Department of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, MalaysiaThe threat of influenza A virus (IAV) remains an annual health concern, as almost 500,000 people die each year due to the seasonal flu. Current flu vaccines are highly dependent on embryonated chicken eggs for production, which is time consuming and costly. These vaccines only confer moderate protections in elderly people, and they lack cross-protectivity; thereby requiring annual reformulation to ensure effectiveness against contemporary circulating strains. To address current limitations, new strategies are being sought, with great emphasis given on exploiting IAV's conserved antigens for vaccine development, and by using different vaccine technologies to enhance immunogenicity and expedite vaccine production. Among these technologies, there are growing pre-clinical and clinical studies involving virus-like particles (VLPs), as they are capable to display multiple conserved IAV antigens and augment their immune responses. In this review, we outline recent findings involving broadly effective IAV antigens and strategies to display these antigens on VLPs. Current production systems for IAV VLP vaccines are comprehensively reviewed. Pain-free methods for administration of IAV VLP vaccines through intranasal and transdermal routes, as well as the mechanisms in stimulating immune responses are discussed in detail. The future perspectives of VLPs in IAV vaccine development are discussed, particularly concerning their potentials in overcoming current immunological limitations of IAV vaccines, and their inherent advantages in exploring intranasal vaccination studies. We also propose avenues to expedite VLP vaccine production, as we envision that there will be more clinical trials involving IAV VLP vaccines, leading to commercialization of these vaccines in the near future.http://www.sciencedirect.com/science/article/pii/S2666517424001007Virus-like particleInfluenza A virusVaccineConserved antigensPain-freeProduction system
spellingShingle Jaffar Ali Muhamad Norizwan
Wen Siang Tan
Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccines
Current Research in Microbial Sciences
Virus-like particle
Influenza A virus
Vaccine
Conserved antigens
Pain-free
Production system
title Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccines
title_full Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccines
title_fullStr Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccines
title_full_unstemmed Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccines
title_short Multifaceted virus-like particles: Navigating towards broadly effective influenza A virus vaccines
title_sort multifaceted virus like particles navigating towards broadly effective influenza a virus vaccines
topic Virus-like particle
Influenza A virus
Vaccine
Conserved antigens
Pain-free
Production system
url http://www.sciencedirect.com/science/article/pii/S2666517424001007
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