Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological Synapse

To circumvent pathology caused by infectious microbes and tumor growth, the host immune system must constantly clear harmful microorganisms and potentially malignant transformed cells. This task is accomplished in part by T-cells, which can directly kill infected or tumorigenic cells. A crucial even...

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Main Authors: Pablo A. González, Leandro J. Carreño, Pablo F. Céspedes, Susan M. Bueno, Claudia A. Riedel, Alexis M. Kalergis
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2013/450291
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author Pablo A. González
Leandro J. Carreño
Pablo F. Céspedes
Susan M. Bueno
Claudia A. Riedel
Alexis M. Kalergis
author_facet Pablo A. González
Leandro J. Carreño
Pablo F. Céspedes
Susan M. Bueno
Claudia A. Riedel
Alexis M. Kalergis
author_sort Pablo A. González
collection DOAJ
description To circumvent pathology caused by infectious microbes and tumor growth, the host immune system must constantly clear harmful microorganisms and potentially malignant transformed cells. This task is accomplished in part by T-cells, which can directly kill infected or tumorigenic cells. A crucial event determining the recognition and elimination of detrimental cells is antigen recognition by the T cell receptor (TCR) expressed on the surface of T cells. Upon binding of the TCR to cognate peptide-MHC complexes presented on the surface of antigen presenting cells (APCs), a specialized supramolecular structure known as the immunological synapse (IS) assembles at the T cell-APC interface. Such a structure involves massive redistribution of membrane proteins, including TCR/pMHC complexes, modulatory receptor pairs, and adhesion molecules. Furthermore, assembly of the immunological synapse leads to intracellular events that modulate and define the magnitude and characteristics of the T cell response. Here, we discuss recent literature on the regulation and assembly of IS and the mechanisms evolved by tumors to modulate its function to escape T cell cytotoxicity, as well as novel strategies targeting the IS for therapy.
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language English
publishDate 2013-01-01
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series Clinical and Developmental Immunology
spelling doaj-art-fa3e0aef61b445a4ba07e34dd29a2f132025-02-03T06:05:20ZengWileyClinical and Developmental Immunology1740-25221740-25302013-01-01201310.1155/2013/450291450291Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological SynapsePablo A. González0Leandro J. Carreño1Pablo F. Céspedes2Susan M. Bueno3Claudia A. Riedel4Alexis M. Kalergis5Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Avenida Libertador Bernardo O'Higgins no. 340, Santiago 8331010, ChileMillennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Avenida Libertador Bernardo O'Higgins no. 340, Santiago 8331010, ChileMillennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Avenida Libertador Bernardo O'Higgins no. 340, Santiago 8331010, ChileMillennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Avenida Libertador Bernardo O'Higgins no. 340, Santiago 8331010, ChileMillennium Institute on Immunology and Immunotherapy, Departamento de Ciencias Biológicas, Facultad de Ciencias Biológicas y Facultad de Medicina, Universidad Andrés Bello, ChileMillennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Avenida Libertador Bernardo O'Higgins no. 340, Santiago 8331010, ChileTo circumvent pathology caused by infectious microbes and tumor growth, the host immune system must constantly clear harmful microorganisms and potentially malignant transformed cells. This task is accomplished in part by T-cells, which can directly kill infected or tumorigenic cells. A crucial event determining the recognition and elimination of detrimental cells is antigen recognition by the T cell receptor (TCR) expressed on the surface of T cells. Upon binding of the TCR to cognate peptide-MHC complexes presented on the surface of antigen presenting cells (APCs), a specialized supramolecular structure known as the immunological synapse (IS) assembles at the T cell-APC interface. Such a structure involves massive redistribution of membrane proteins, including TCR/pMHC complexes, modulatory receptor pairs, and adhesion molecules. Furthermore, assembly of the immunological synapse leads to intracellular events that modulate and define the magnitude and characteristics of the T cell response. Here, we discuss recent literature on the regulation and assembly of IS and the mechanisms evolved by tumors to modulate its function to escape T cell cytotoxicity, as well as novel strategies targeting the IS for therapy.http://dx.doi.org/10.1155/2013/450291
spellingShingle Pablo A. González
Leandro J. Carreño
Pablo F. Céspedes
Susan M. Bueno
Claudia A. Riedel
Alexis M. Kalergis
Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological Synapse
Clinical and Developmental Immunology
title Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological Synapse
title_full Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological Synapse
title_fullStr Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological Synapse
title_full_unstemmed Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological Synapse
title_short Modulation of Tumor Immunity by Soluble and Membrane-Bound Molecules at the Immunological Synapse
title_sort modulation of tumor immunity by soluble and membrane bound molecules at the immunological synapse
url http://dx.doi.org/10.1155/2013/450291
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