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APC licensing and CD4+T cell help in liver-stage malaria

Malaria parasites spend a critical phase of their life cycle inside hepatocytes, in an environment with complex and distinctive immunological features. Here I will discuss how the immunological features of the liver and the adaptations of malaria parasites interact, resulting in defective CD8+ T cel...

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Detalles Bibliográficos
Autor principal: Crispe, Ian N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227505/
https://www.ncbi.nlm.nih.gov/pubmed/25426113
http://dx.doi.org/10.3389/fmicb.2014.00617
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author Crispe, Ian N.
author_facet Crispe, Ian N.
author_sort Crispe, Ian N.
collection PubMed
description Malaria parasites spend a critical phase of their life cycle inside hepatocytes, in an environment with complex and distinctive immunological features. Here I will discuss how the immunological features of the liver and the adaptations of malaria parasites interact, resulting in defective CD8+ T cell immunity. These processes are explored with a focus on the mechanism by which CD4+ T cells deliver help to CD8+ T cells, and specifically through their interaction with antigen-presenting cells (APCs), resulting in “licensing” of the APCs and enhanced capacity to optimally activate CD8+ T cells. Synthesis of the available evidence supports a model in which the parasite-mediated manipulation of programmed cell death in infected hepatocytes impairs the capacity of the liver’s immune system to successfully license APCs and fully activate T cell immunity.
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spelling pubmed-42275052014-11-25 APC licensing and CD4+T cell help in liver-stage malaria Crispe, Ian N. Front Microbiol Microbiology Malaria parasites spend a critical phase of their life cycle inside hepatocytes, in an environment with complex and distinctive immunological features. Here I will discuss how the immunological features of the liver and the adaptations of malaria parasites interact, resulting in defective CD8+ T cell immunity. These processes are explored with a focus on the mechanism by which CD4+ T cells deliver help to CD8+ T cells, and specifically through their interaction with antigen-presenting cells (APCs), resulting in “licensing” of the APCs and enhanced capacity to optimally activate CD8+ T cells. Synthesis of the available evidence supports a model in which the parasite-mediated manipulation of programmed cell death in infected hepatocytes impairs the capacity of the liver’s immune system to successfully license APCs and fully activate T cell immunity. Frontiers Media S.A. 2014-11-11 /pmc/articles/PMC4227505/ /pubmed/25426113 http://dx.doi.org/10.3389/fmicb.2014.00617 Text en Copyright © 2014 Crispe. http://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) or licensor 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 Microbiology
Crispe, Ian N.
APC licensing and CD4+T cell help in liver-stage malaria
title APC licensing and CD4+T cell help in liver-stage malaria
title_full APC licensing and CD4+T cell help in liver-stage malaria
title_fullStr APC licensing and CD4+T cell help in liver-stage malaria
title_full_unstemmed APC licensing and CD4+T cell help in liver-stage malaria
title_short APC licensing and CD4+T cell help in liver-stage malaria
title_sort apc licensing and cd4+t cell help in liver-stage malaria
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227505/
https://www.ncbi.nlm.nih.gov/pubmed/25426113
http://dx.doi.org/10.3389/fmicb.2014.00617
work_keys_str_mv AT crispeiann apclicensingandcd4tcellhelpinliverstagemalaria