Overview
- Editors:
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Michael P. Cancro
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School of Medicine, University of Pennsylvania, Philadelphia, U.S.A.
- The discovery of BLy.
- S may lead to therapies for several diseases that involve B cells, including immune deficiencies, autoimmune disease and B cell tumors
- Includes supplementary material: sn.pub/extras
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Table of contents (12 chapters)
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Front Matter
Pages i-xiii
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- Wasif N. Khan, Nicholas P. Shinners, Iris Castro, Kristen L. Hoek
Pages 19-41
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- Sandra Gardam, Robert Brink
Pages 43-63
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- Andrea Cerutti, Kang Chen
Pages 65-92
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- Joanne M. Hildebrand, Ping Xie, Gail A. Bishop
Pages 93-114
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- Fabienne Mackay, William A. Figgett, Pali Verma, Xavier Mariette
Pages 125-160
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- Stuart G. Tangye, David A Fulcher
Pages 195-220
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- Lachy McLean, Dhaya Seshasayee, Susan L. Kalled, Flavius Martin
Pages 221-243
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- Lingchen Fu, Lan V. Pham, Yen-chiu Lin-Lee, Archito T. Tamayo, Richard J. Ford
Pages 245-263
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- Anne J. Novak, Stephen M. Ansell
Pages 265-282
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Back Matter
Pages 283-289
About this book
Discovery of the BLyS (also known as BAFF) family of ligands and receptors has yielded a paradigm shift in our view of B-lymphocyte selection, survival, activation, and homeostasis. Previously, the B-cell antigen receptor (BCR) was viewed as the sole mediator of these parameters, in which BCR signals were not only dominant but were also linearly related to consequent outcomes. However, appreciating that BLyS signaling is an equal partner in establishing and maintaining B-cell pools in- cated that additional regulatory complexity – apparently based on population density and homeostatic demands – had to be included in models of B-cell behavior. This mounting interest was ampli?ed by evidence of a clear relationship to autoim- nity. The resulting ?urry of research activity has yielded a wealth of information and insights, impacting basic concepts in B-cell tolerance and activation as well as revealing novel translational strategies for autoimmunity, neoplasia, and transplant tolerance. This book includes 12 chapters that together yield an overview of these advances and ideas. The initial excitement generated by associations with humoral autoimmunity, coupled with profound B lineage phenotypes in knockout mouse models, prompted immediate questions: What do these receptors and cytokines look like, how do they interact, what cells express them, and how does this inform our understating of their biology? Indeed, probing the structural features of BLyS family ligands and rec- tors has afforded substantial insight, as have studies directed toward understanding the basic biological actions of these molecules.
Editors and Affiliations
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School of Medicine, University of Pennsylvania, Philadelphia, U.S.A.
Michael P. Cancro
