Advances in Immunology, Volume 134, the latest release in a long-established and highly respected publication, presents current developments and comprehensive reviews in immunology. Topics covered in this new volume include γδ T Cells and B Cells, A Chemoattractant-Guided Walk Through Lymphopoiesis: From Hematopoietic Stem Cells to Mature B Lymphocytes. Tissue Specific Regulation of Dendritic Cell Development and Function, and the Regulation of Innate and Adaptive Immunity by Transforming Growth Factor Beta (TGFβ). Articles in this long running series 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.
1. Cover image - p. iv 2. Title page - p. iv 3. Table of Contents - p. iv 4. Copyright - p. iv 5. Contributors - p. vii 6. Chapter One: γδ T Cells and B Cells - p. vii 7. Chapter Two: A Chemoattractant-Guided Walk Through Lymphopoiesis: From Hematopoietic Stem Cells to Mature B Lymphocytes - p. 45 8. Chapter Three: Tissue-Specific Diversity and Functions of Conventional Dendritic Cells - p. 88 9. Chapter Four: Regulation of Innate and Adaptive Immunity by TGFβ - p. 135 10. Chapter Five: Humanized Immunoglobulin Mice: Models for HIV Vaccine Testing and Studying the Broadly Neutralizing Antibody Problem - p. 233 11. Abstract - p. 236 12. 1 Overview of the Current State of HIV Vaccine Research - p. 237 13. 2 Characteristics of bnAbs Isolated During Infection and Their Env Targets: Clues for Vaccine Design - p. 239 14. 3 Current Gaps in HIV Vaccinology - p. 251 15. 4 Human Ig KI Models in Elucidating bnAb Tolerance Controls and Testing Ways to Overcome Them - p. 266 16. 5 bnAb KI Models for Testing New HIV Vaccine Strategies - p. 286 17. 6 Ig KI-Related Methodological Advances Relevant for Studying bnAb Development - p. 318 18. 7 Perspectives - p. 333 19. Acknowledgments - p. 335
Advances in Immunology, Volume 134, the latest release in a long-established and highly respected publication, presents current developments and comprehensive reviews in immunology. Topics covered in this new volume include γδ T Cells and B Cells, A Chemoattractant-Guided Walk Through Lymphopoiesis: From Hematopoietic Stem Cells to Mature B Lymphocytes. Tissue Specific Regulation of Dendritic Cell Development and Function, and the Regulation of Innate and Adaptive Immunity by Transforming Growth Factor Beta (TGFβ). Articles in this long running series 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.
1. Cover image - p. iv 2. Title page - p. iv 3. Table of Contents - p. iv 4. Copyright - p. iv 5. Contributors - p. vii 6. Chapter One: γδ T Cells and B Cells - p. vii 7. Chapter Two: A Chemoattractant-Guided Walk Through Lymphopoiesis: From Hematopoietic Stem Cells to Mature B Lymphocytes - p. 45 8. Chapter Three: Tissue-Specific Diversity and Functions of Conventional Dendritic Cells - p. 88 9. Chapter Four: Regulation of Innate and Adaptive Immunity by TGFβ - p. 135 10. Chapter Five: Humanized Immunoglobulin Mice: Models for HIV Vaccine Testing and Studying the Broadly Neutralizing Antibody Problem - p. 233 11. Abstract - p. 236 12. 1 Overview of the Current State of HIV Vaccine Research - p. 237 13. 2 Characteristics of bnAbs Isolated During Infection and Their Env Targets: Clues for Vaccine Design - p. 239 14. 3 Current Gaps in HIV Vaccinology - p. 251 15. 4 Human Ig KI Models in Elucidating bnAb Tolerance Controls and Testing Ways to Overcome Them - p. 266 16. 5 bnAb KI Models for Testing New HIV Vaccine Strategies - p. 286 17. 6 Ig KI-Related Methodological Advances Relevant for Studying bnAb Development - p. 318 18. 7 Perspectives - p. 333 19. Acknowledgments - p. 335
