Advances in Immunology - 1st Edition - ISBN: 9780128124093, 9780128124109

Advances in Immunology, Volume 133

1st Edition

Serial Editors: Frederick Alt
eBook ISBN: 9780128124109
Hardcover ISBN: 9780128124093
Imprint: Academic Press
Published Date: 20th February 2017
Page Count: 242
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Table of Contents

Chapter One: Macrophages and Mitochondria: A Critical Interplay Between Metabolism, Signaling, and the Functional Activity

  • Abstract
  • 1 Introduction
  • 2 Mitochondrial Metabolism Governs Macrophage Activation State
  • 3 Mitochondrial ROS in Innate Immune Responses
  • 4 Mitochondrial-Mediated Antiviral Immunity
  • 5 Inflammasome Activation and Mitochondria
  • 6 Concluding Remarks
  • Acknowledgments

Chapter Two: Molecular Mechanisms of Somatic Hypermutation and Class Switch Recombination

  • Abstract
  • 1 Antibody Diversification During the Humoral Response
  • 2 Molecular Mechanisms of SHM and CSR
  • 3 DNA Deamination at the Igs
  • 4 AID Initiates a DNA Repair Cascade
  • 5 Postdeamination Roles of AID?
  • 6 Perspectives
  • Acknowledgments

Chapter Three: Emerging Major Histocompatibility Complex Class I-Related Functions of NLRC5

  • Abstract
  • 1 Background
  • 2 Lessons From CIITA
  • 3 NLRC5 and Its Role in Regulating MHC Class I Levels
  • 4 NLRC5 and Its Emerging Roles in Health and Disease
  • 5 Concluding Remarks
  • Acknowledgments

Chapter Four: Nucleic Acid Immunity

  • Abstract
  • 1 Introduction
  • 2 Principles of Nucleic Acid Immunity in Different Species
  • 3 Historic Overview of Different Fields Merging Into Nucleic Acid Immunity
  • 4 Functional Components of Nucleic Acid Immunity
  • 5 Innate and Adaptive Components in Nucleic Acid Immunity
  • 6 Innate and Adaptive Nucleic Acid Immunity in Prokaryotes
  • 7 Receptors and Nucleases Not Involving Classical Immune Functions
  • 8 RNA Interference
  • 9 Immune-Sensing Receptors
  • 10 Conclusions
  • Acknowledgments

Chapter Five: About Training and Memory: NK-Cell Adaptation to Viral Infections



Advances in Immunology, Volume 133, the latest release in this long-established and highly respected publication, presents current developments and comprehensive reviews in immunology. Articles address the wide range of topics that comprise immunology, including molecular and cellular activation mechanisms, phylogeny and molecular evolution, and clinical modalities. Edited and authored by the foremost scientists in the field, each volume provides up-to-date information and directions for the future.

Key Features

  • Contains contributions from leading authorities
  • Informs and updates on all the latest developments in the field of immunology
  • Addresses molecular and cellular activation mechanisms, phylogeny and molecular evolution, and clinical modalities


Immunologists and infectious disease specialists, cell biologists and hematologists


No. of pages:
© Academic Press 2017
Academic Press
eBook ISBN:
Hardcover ISBN:

Ratings and Reviews

About the Serial Editors

Frederick Alt Serial Editor

Frederick Alt received his Ph.D. in Biology from Stanford University in 1977 where he worked with Robert Schimke and discovered gene amplification and genomic instability in mammalian cancer cells. Alt moved to MIT for postdoctoral work with David Baltimore, where he helped elucidate basic principles of recombination in the immune system. His work with Baltimore included the discovery that production of membrane versus secreted immunoglobulin is achieved via differential RNA processing and the discovery that allelic exclusion of Immunoglobulin (Ig) gene rearrangements is controlled by feedback from protein products. With Baltimore, Alt also elucidated major aspects of the V(D)J recombination mechanism, including involvement of site-specific DNA double strand breaks (DSBs) that are end joined, and the discovery of ”N” regions, which represent a major source of antigen receptor diversity.

Dr. Alt moved to Columbia University in 1982 as Assistant Professor of Biochemistry. He became Professor of Biochemistry and Molecular Biophysics in 1985 and HHMI Investigator in 1987. At Columbia, he established the role of Ig chains in regulating B cell development and discovered that antigen receptor genes are assembled by a common V(D)J recombinase. He then elucidated a role for non-coding gene transcription and "chromatin accessibility" as means to target the lineage, stage, and allele specific activity of the V(D)J recombinase. He extended that work to show that IgH class switch recombination (CSR) is B cells to particular IgH classes is directed by activation of non-coding transcription units that contain the CSR target sequences. At Columbia, he also discovered N-myc, based on its amplification in human neuroblastomas and he characterized the Myc cellular oncogene family.

In 1991, Dr. Alt moved to Boston Children' Hospital (BCH) and Harvard Medical School as a Professor of Genetics and HHMI Investigator. He also became a Senior Investigator at

Affiliations and Expertise

Harvard Medical School, Boston, MA, USA