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Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine
Next-generation vaccines that utilize T cells could potentially overcome the limitations of current influenza vaccines that rely on antibodies to provide narrow subtype-specific protection and are prone to antigenic mismatch with circulating strains. Evidence from animal models shows that T cells ca...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027237/ https://www.ncbi.nlm.nih.gov/pubmed/29587436 http://dx.doi.org/10.3390/vaccines6020018 |
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author | Clemens, E. Bridie van de Sandt, Carolien Wong, Sook San Wakim, Linda M. Valkenburg, Sophie A. |
author_facet | Clemens, E. Bridie van de Sandt, Carolien Wong, Sook San Wakim, Linda M. Valkenburg, Sophie A. |
author_sort | Clemens, E. Bridie |
collection | PubMed |
description | Next-generation vaccines that utilize T cells could potentially overcome the limitations of current influenza vaccines that rely on antibodies to provide narrow subtype-specific protection and are prone to antigenic mismatch with circulating strains. Evidence from animal models shows that T cells can provide heterosubtypic protection and are crucial for immune control of influenza virus infections. This has provided hope for the design of a universal vaccine able to prime against diverse influenza virus strains and subtypes. However, multiple hurdles exist for the realisation of a universal T cell vaccine. Overall primary concerns are: extrapolating human clinical studies, seeding durable effective T cell resident memory (Trm), population human leucocyte antigen (HLA) coverage, and the potential for T cell-mediated immune escape. Further comprehensive human clinical data is needed during natural infection to validate the protective role T cells play during infection in the absence of antibodies. Furthermore, fundamental questions still exist regarding the site, longevity and duration, quantity, and phenotype of T cells needed for optimal protection. Standardised experimental methods, and eventually simplified commercial assays, to assess peripheral influenza-specific T cell responses are needed for larger-scale clinical studies of T cells as a correlate of protection against influenza infection. The design and implementation of a T cell-inducing vaccine will require a consensus on the level of protection acceptable in the community, which may not provide sterilizing immunity but could protect the individual from severe disease, reduce the length of infection, and potentially reduce transmission in the community. Therefore, increasing the standard of care potentially offered by T cell vaccines should be considered in the context of pandemic preparedness and zoonotic infections, and in combination with improved antibody vaccine targeting methods. Current pandemic vaccine preparedness measures and ongoing clinical trials under-utilise T cell-inducing vaccines, reflecting the myriad questions that remain about how, when, where, and which T cells are needed to fight influenza virus infection. This review aims to bring together basic fundamentals of T cell biology with human clinical data, which need to be considered for the implementation of a universal vaccine against influenza that harnesses the power of T cells. |
format | Online Article Text |
id | pubmed-6027237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60272372018-07-13 Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine Clemens, E. Bridie van de Sandt, Carolien Wong, Sook San Wakim, Linda M. Valkenburg, Sophie A. Vaccines (Basel) Review Next-generation vaccines that utilize T cells could potentially overcome the limitations of current influenza vaccines that rely on antibodies to provide narrow subtype-specific protection and are prone to antigenic mismatch with circulating strains. Evidence from animal models shows that T cells can provide heterosubtypic protection and are crucial for immune control of influenza virus infections. This has provided hope for the design of a universal vaccine able to prime against diverse influenza virus strains and subtypes. However, multiple hurdles exist for the realisation of a universal T cell vaccine. Overall primary concerns are: extrapolating human clinical studies, seeding durable effective T cell resident memory (Trm), population human leucocyte antigen (HLA) coverage, and the potential for T cell-mediated immune escape. Further comprehensive human clinical data is needed during natural infection to validate the protective role T cells play during infection in the absence of antibodies. Furthermore, fundamental questions still exist regarding the site, longevity and duration, quantity, and phenotype of T cells needed for optimal protection. Standardised experimental methods, and eventually simplified commercial assays, to assess peripheral influenza-specific T cell responses are needed for larger-scale clinical studies of T cells as a correlate of protection against influenza infection. The design and implementation of a T cell-inducing vaccine will require a consensus on the level of protection acceptable in the community, which may not provide sterilizing immunity but could protect the individual from severe disease, reduce the length of infection, and potentially reduce transmission in the community. Therefore, increasing the standard of care potentially offered by T cell vaccines should be considered in the context of pandemic preparedness and zoonotic infections, and in combination with improved antibody vaccine targeting methods. Current pandemic vaccine preparedness measures and ongoing clinical trials under-utilise T cell-inducing vaccines, reflecting the myriad questions that remain about how, when, where, and which T cells are needed to fight influenza virus infection. This review aims to bring together basic fundamentals of T cell biology with human clinical data, which need to be considered for the implementation of a universal vaccine against influenza that harnesses the power of T cells. MDPI 2018-03-26 /pmc/articles/PMC6027237/ /pubmed/29587436 http://dx.doi.org/10.3390/vaccines6020018 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Clemens, E. Bridie van de Sandt, Carolien Wong, Sook San Wakim, Linda M. Valkenburg, Sophie A. Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine |
title | Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine |
title_full | Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine |
title_fullStr | Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine |
title_full_unstemmed | Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine |
title_short | Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine |
title_sort | harnessing the power of t cells: the promising hope for a universal influenza vaccine |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027237/ https://www.ncbi.nlm.nih.gov/pubmed/29587436 http://dx.doi.org/10.3390/vaccines6020018 |
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