Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine Design

Recurrent S. aureus infections are common, suggesting that natural immune responses are not protective. All candidate vaccines tested thus far have failed to protect against S. aureus infections, highlighting an urgent need to better understand the mechanisms by which the bacterium interacts with th...

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Main Authors: Omid Teymournejad, Christopher P. Montgomery
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2021.633672/full
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spelling doaj-592820be692145ea88a76d355af783722021-02-22T04:58:23ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-02-011210.3389/fimmu.2021.633672633672Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine DesignOmid Teymournejad0Christopher P. Montgomery1Christopher P. Montgomery2Center for Microbial Pathogenesis, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, United StatesCenter for Microbial Pathogenesis, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, United StatesDepartment of Pediatrics, The Ohio State University College of Medicine, Columbus, OH, United StatesRecurrent S. aureus infections are common, suggesting that natural immune responses are not protective. All candidate vaccines tested thus far have failed to protect against S. aureus infections, highlighting an urgent need to better understand the mechanisms by which the bacterium interacts with the host immune system to evade or prevent protective immunity. Although there is evidence in murine models that both cellular and humoral immune responses are important for protection against S. aureus, human studies suggest that T cells are critical in determining susceptibility to infection. This review will use an “anatomic” approach to systematically outline the steps necessary in generating a T cell-mediated immune response against S. aureus. Through the processes of bacterial uptake by antigen presenting cells, processing and presentation of antigens to T cells, and differentiation and proliferation of memory and effector T cell subsets, the ability of S. aureus to evade or inhibit each step of the T-cell mediated response will be reviewed. We hypothesize that these interactions result in the redirection of immune responses away from protective antigens, thereby precluding the establishment of “natural” memory and potentially inhibiting the efficacy of vaccination. It is anticipated that this approach will reveal important implications for future design of vaccines to prevent these infections.https://www.frontiersin.org/articles/10.3389/fimmu.2021.633672/fullS. aureusvaccineT cellantigen presenting cell (APC)human leukocyte antigen (HLA)
collection DOAJ
language English
format Article
sources DOAJ
author Omid Teymournejad
Christopher P. Montgomery
Christopher P. Montgomery
spellingShingle Omid Teymournejad
Christopher P. Montgomery
Christopher P. Montgomery
Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine Design
Frontiers in Immunology
S. aureus
vaccine
T cell
antigen presenting cell (APC)
human leukocyte antigen (HLA)
author_facet Omid Teymournejad
Christopher P. Montgomery
Christopher P. Montgomery
author_sort Omid Teymournejad
title Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine Design
title_short Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine Design
title_full Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine Design
title_fullStr Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine Design
title_full_unstemmed Evasion of Immunological Memory by S. aureus Infection: Implications for Vaccine Design
title_sort evasion of immunological memory by s. aureus infection: implications for vaccine design
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2021-02-01
description Recurrent S. aureus infections are common, suggesting that natural immune responses are not protective. All candidate vaccines tested thus far have failed to protect against S. aureus infections, highlighting an urgent need to better understand the mechanisms by which the bacterium interacts with the host immune system to evade or prevent protective immunity. Although there is evidence in murine models that both cellular and humoral immune responses are important for protection against S. aureus, human studies suggest that T cells are critical in determining susceptibility to infection. This review will use an “anatomic” approach to systematically outline the steps necessary in generating a T cell-mediated immune response against S. aureus. Through the processes of bacterial uptake by antigen presenting cells, processing and presentation of antigens to T cells, and differentiation and proliferation of memory and effector T cell subsets, the ability of S. aureus to evade or inhibit each step of the T-cell mediated response will be reviewed. We hypothesize that these interactions result in the redirection of immune responses away from protective antigens, thereby precluding the establishment of “natural” memory and potentially inhibiting the efficacy of vaccination. It is anticipated that this approach will reveal important implications for future design of vaccines to prevent these infections.
topic S. aureus
vaccine
T cell
antigen presenting cell (APC)
human leukocyte antigen (HLA)
url https://www.frontiersin.org/articles/10.3389/fimmu.2021.633672/full
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