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Fc Receptors

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Cover of 'Fc Receptors'

Table of Contents

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    Book Overview
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    Chapter 1 The Old but New IgM Fc Receptor (Fc μ R)
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    Chapter 2 Emerging Roles for the FCRL Family Members in Lymphocyte Biology and Disease.
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    Chapter 3 Intracellular Antibody Immunity and the Cytosolic Fc Receptor TRIM21.
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    Chapter 4 Computational Modeling of the Main Signaling Pathways Involved in Mast Cell Activation
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    Chapter 5 Calcium Channels in Fc Receptor Signaling
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    Chapter 6 Regulation of FcεRI Signaling by Lipid Phosphatases.
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    Chapter 7 Fc receptors as adaptive immunoreceptors.
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    Chapter 8 Glycosylation and fc receptors.
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    Chapter 9 Antibodies as Natural Adjuvants
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    Chapter 10 IgA, IgA Receptors, and Their Anti-inflammatory Properties.
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    Chapter 11 Humanized Mice to Study FcγR Function.
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    Chapter 12 FcRn: From Molecular Interactions to Regulation of IgG Pharmacokinetics and Functions.
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    Chapter 13 Human FcR Polymorphism and Disease
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    Chapter 14 Bridging autoantibodies and arthritis: the role of fc receptors.
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    Chapter 15 The FcγR of Humans and Non-human Primates and Their Interaction with IgG: Implications for Induction of Inflammation, Resistance to Infection and the Use of Therapeutic Monoclonal Antibodies
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    Chapter 16 FcγRIIB as a Key Determinant of Agonistic Antibody Efficacy.
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    Chapter 17 Fc receptor-dependent mechanisms of monoclonal antibody therapy of cancer.
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    Chapter 18 Sweet and Sour: The Role of Glycosylation for the Anti-inflammatory Activity of Immunoglobulin G.
Attention for Chapter 14: Bridging autoantibodies and arthritis: the role of fc receptors.
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Chapter title
Bridging autoantibodies and arthritis: the role of fc receptors.
Chapter number 14
Book title
Fc Receptors
Published in
Current topics in microbiology and immunology, August 2014
DOI 10.1007/978-3-319-07911-0_14
Pubmed ID
Book ISBNs
978-3-31-907910-3, 978-3-31-907911-0
Authors

El Bannoudi H, Ioan-Facsinay A, Toes RE, Hanane el Bannoudi, Andreea Ioan-Facsinay, René E. M. Toes, Bannoudi, Hanane el, Ioan-Facsinay, Andreea, Toes, René E. M.

Abstract

Autoantibodies represent a hallmark of Rheumatoid arthritis (RA), which is a chronic inflammatory autoimmune disease characterized by inflammation and damage in the joints. Anti-Citrullinated Protein Antibodies (ACPA) are the most prominent autoantibodies present in RA patients. These autoantibodies have been intensively investigated during the last 20 years due to their diagnostic and predictive value. Furthermore, they are believed to be involved in mediating the damage associated with RA. Antibodies of the IgG isotype interact with the immune system via Fcγ receptors expressed on immune cells as well as nonimmune cells. These receptors, therefore, form the bridge between Fcγ receptor-positive cells and antibodies complexed to antigen allowing the modulation and activation of cellular immune responses that are involved in immune defense against invading microorganisms. However, in case triggered by antibodies against self-antigens, they can also play a pivotal role in the induction and perpetuation of autoimmune diseases such as RA. Mouse models have been indispensably important for understanding the role of Fcγ receptors in the development of arthritis. Here we discuss the contribution of autoantibodies to the pathogenesis of arthritis in preclinical animal models, as well as RA, in relation to their interaction with the different (immune inhibitory and activating) Fcγ receptors.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Italy 1 9%
Unknown 10 91%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 36%
Student > Doctoral Student 2 18%
Student > Master 2 18%
Professor 1 9%
Librarian 1 9%
Other 0 0%
Unknown 1 9%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 36%
Medicine and Dentistry 2 18%
Immunology and Microbiology 2 18%
Pharmacology, Toxicology and Pharmaceutical Science 1 9%
Arts and Humanities 1 9%
Other 0 0%
Unknown 1 9%