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Birkhäuser
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The Immune Synapse as a Novel Target for Therapy

  • Book
  • © 2008

Overview

  • Discusses how interfering with T cell activation may lead to immune tolerance
  • Describes immune modulation and the recruitment of regulatory T cells
  • Provides information on the role of monoclonal antibodies in tolerance induction
  • Describes mechanisms maintaining dominant tolerance
  • Includes supplementary material: sn.pub/extras

Part of the book series: Progress in Inflammation Research (PIR)

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Table of contents (12 chapters)

Keywords

About this book

It is now accepted that T cell activation by an antigen-presenting cell requires the organization of a supramolecular structure – the immune synapse. This structure, with different types of molecules spatially segregated, is involved in the delivery of quantitative and qualitative signals critical for T cell activation, and therefore in controlling the nature of the immune response. This volume discusses the progress in manipulating components of the immune synapse as a strategy to regulate the immune response in immune pathology, such as transplantation, autoimmunity and allergy. Donnadieu reviews the current knowledge on the molecular composition and organization of the immune synapse and how the formation of this structure can be modulated by chemokines. It is also known that the immune synapse formation is critical for the activation of naive T cells, as well as their functional polarization. The second chapter discusses the conversion of naive T cells into regulatory T cells (Treg) when components of the immune synapse are manipulated in such a way that the T cells receive suboptimal activation signals.

Editors and Affiliations

  • Unidade de Imunologia Celular Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal

    Luis Graca

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