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The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens
Similar to other pathogens, bacteria have developed during their evolution a variety of mechanisms to overcome both innate and acquired immunity, accounting for their ability to cause disease or chronic infections. The mechanisms exploited for this critical function act by targeting conserved struct...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325968/ https://www.ncbi.nlm.nih.gov/pubmed/35911720 http://dx.doi.org/10.3389/fimmu.2022.943344 |
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author | Capitani, Nagaja Baldari, Cosima T. |
author_facet | Capitani, Nagaja Baldari, Cosima T. |
author_sort | Capitani, Nagaja |
collection | PubMed |
description | Similar to other pathogens, bacteria have developed during their evolution a variety of mechanisms to overcome both innate and acquired immunity, accounting for their ability to cause disease or chronic infections. The mechanisms exploited for this critical function act by targeting conserved structures or pathways that regulate the host immune response. A strategic potential target is the immunological synapse (IS), a highly specialized structure that forms at the interface between antigen presenting cells (APC) and T lymphocytes and is required for the establishment of an effective T cell response to the infectious agent and for the development of long-lasting T cell memory. While a variety of bacterial pathogens are known to impair or subvert cellular processes essential for antigen processing and presentation, on which IS assembly depends, it is only recently that the possibility that IS may be a direct target of bacterial virulence factors has been considered. Emerging evidence strongly supports this notion, highlighting IS targeting as a powerful, novel means of immune evasion by bacterial pathogens. In this review we will present a brief overview of the mechanisms used by bacteria to affect IS assembly by targeting APCs. We will then summarize what has emerged from the current handful of studies that have addressed the direct impact of bacterial virulence factors on IS assembly in T cells and, based on the strategic cellular processes targeted by these factors in other cell types, highlight potential IS-related vulnerabilities that could be exploited by these pathogens to evade T cell mediated immunity. |
format | Online Article Text |
id | pubmed-9325968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93259682022-07-28 The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens Capitani, Nagaja Baldari, Cosima T. Front Immunol Immunology Similar to other pathogens, bacteria have developed during their evolution a variety of mechanisms to overcome both innate and acquired immunity, accounting for their ability to cause disease or chronic infections. The mechanisms exploited for this critical function act by targeting conserved structures or pathways that regulate the host immune response. A strategic potential target is the immunological synapse (IS), a highly specialized structure that forms at the interface between antigen presenting cells (APC) and T lymphocytes and is required for the establishment of an effective T cell response to the infectious agent and for the development of long-lasting T cell memory. While a variety of bacterial pathogens are known to impair or subvert cellular processes essential for antigen processing and presentation, on which IS assembly depends, it is only recently that the possibility that IS may be a direct target of bacterial virulence factors has been considered. Emerging evidence strongly supports this notion, highlighting IS targeting as a powerful, novel means of immune evasion by bacterial pathogens. In this review we will present a brief overview of the mechanisms used by bacteria to affect IS assembly by targeting APCs. We will then summarize what has emerged from the current handful of studies that have addressed the direct impact of bacterial virulence factors on IS assembly in T cells and, based on the strategic cellular processes targeted by these factors in other cell types, highlight potential IS-related vulnerabilities that could be exploited by these pathogens to evade T cell mediated immunity. Frontiers Media S.A. 2022-07-13 /pmc/articles/PMC9325968/ /pubmed/35911720 http://dx.doi.org/10.3389/fimmu.2022.943344 Text en Copyright © 2022 Capitani and Baldari https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Capitani, Nagaja Baldari, Cosima T. The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens |
title | The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens |
title_full | The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens |
title_fullStr | The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens |
title_full_unstemmed | The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens |
title_short | The Immunological Synapse: An Emerging Target for Immune Evasion by Bacterial Pathogens |
title_sort | immunological synapse: an emerging target for immune evasion by bacterial pathogens |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325968/ https://www.ncbi.nlm.nih.gov/pubmed/35911720 http://dx.doi.org/10.3389/fimmu.2022.943344 |
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