Immunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.

Pathology in most chronic inflammatory diseases is characterized by an imbalance in cytokine expression. Targeting cytokines with monoclonal antibodies has proven to be a highly effective treatment. However, monoclonal antibody therapy has disadvantages such as high production costs, generation of a...

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Opis bibliograficzny
Główni autorzy: Link, A, Bachmann, M
Format: Journal article
Język:English
Wydane: 2010
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author Link, A
Bachmann, M
author_facet Link, A
Bachmann, M
author_sort Link, A
collection OXFORD
description Pathology in most chronic inflammatory diseases is characterized by an imbalance in cytokine expression. Targeting cytokines with monoclonal antibodies has proven to be a highly effective treatment. However, monoclonal antibody therapy has disadvantages such as high production costs, generation of antimonoclonal antibodies and the inconvenience of frequent injections. Therapeutic vaccines have the potential to overcome these limitations. The aim of active vaccination is to induce B-cell responses and obtain autoantibodies capable of neutralizing the interaction of the targeted cytokine with its receptor. In order to achieve this, therapeutic vaccines need to circumvent the potent tolerance mechanisms that exist to prevent immune responses against self-molecules. This article focuses on the tolerance mechanisms of the B- and T-cell compartments and how these may be manipulated to obtain high-affinity autoantibodies without inducing potentially dangerous autoreactive T-cell responses.
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spelling oxford-uuid:2e518330-912c-4d2c-a234-af9c587cf7162022-03-26T12:48:11ZImmunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:2e518330-912c-4d2c-a234-af9c587cf716EnglishSymplectic Elements at Oxford2010Link, ABachmann, MPathology in most chronic inflammatory diseases is characterized by an imbalance in cytokine expression. Targeting cytokines with monoclonal antibodies has proven to be a highly effective treatment. However, monoclonal antibody therapy has disadvantages such as high production costs, generation of antimonoclonal antibodies and the inconvenience of frequent injections. Therapeutic vaccines have the potential to overcome these limitations. The aim of active vaccination is to induce B-cell responses and obtain autoantibodies capable of neutralizing the interaction of the targeted cytokine with its receptor. In order to achieve this, therapeutic vaccines need to circumvent the potent tolerance mechanisms that exist to prevent immune responses against self-molecules. This article focuses on the tolerance mechanisms of the B- and T-cell compartments and how these may be manipulated to obtain high-affinity autoantibodies without inducing potentially dangerous autoreactive T-cell responses.
spellingShingle Link, A
Bachmann, M
Immunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.
title Immunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.
title_full Immunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.
title_fullStr Immunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.
title_full_unstemmed Immunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.
title_short Immunodrugs: breaking B- but not T-cell tolerance with therapeutic anticytokine vaccines.
title_sort immunodrugs breaking b but not t cell tolerance with therapeutic anticytokine vaccines
work_keys_str_mv AT linka immunodrugsbreakingbbutnottcelltolerancewiththerapeuticanticytokinevaccines
AT bachmannm immunodrugsbreakingbbutnottcelltolerancewiththerapeuticanticytokinevaccines