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Books > Medicine > Clinical & internal medicine > Diseases & disorders > Immunology > General
Combinatorial chemistry in conjunction with High Throughput Screening (HTS) is revolutionizing the drug discovery process. Yet, we have much to learn about the integration of these powerful techniques with information from genomics, proteomics, computation and pharmacokinetics before dramatic increases in the drug discovery/development processes can be achieved. The chapters in this book represent the state of the art regarding the integration of combinatorial chemistry and HTS in connection with anti-inflammatory targets. Obviously, there is much work to be done beyond what is described in this text, nevertheless, it should set the stage for creative thinking among scientists of many disciplines for the accomplishment of our ultimate goals in treating inflammatory diseases.
Your Blueprint for Strong Immunity breaks down the science behind our health and shares the secrets of how to be well, for good. Expert immunologist Dr Jenna Macciochi has over 20 years' experience as a scientist researching the impact of lifestyle on the immune system in health and disease. Your Blueprint for Strong Immunity guides you through your very own health MOT and Jenna will help you audit your current lifestyle so you are able to identify key areas that might not be serving your health well. In Part Two, you will learn what to do when you fall ill, how to recover from infection and how to build mental resilience. Part three explains how to support your immunity when you live with chronic illness. She includes over 20 of her own delicious and simple recipes to help you nourish your body. 'What immunologist Dr Jenna Macciochi doesn't know about staying well isn't worth knowing' - Susannah Taylor 'Dr Jenna is one of the most knowledgeable authorities on Immune Health and has a wonderful ability to communicate an incredibly complicated subject in a profoundly approachable and relatable way. ' - Dr Rupy Aujla, author of The Doctor's Kitchen
Explores the course of development of German seroanthropology from its origins in World War I until the end of the Third Reich. Gives an all encompassing interpretation of how the discovery of blood groups in around 1900 galvanised not only old mythologies of blood and origin but also new developments in anthropology and eugenics in the 1920s and 1930s. Boaz portrays how the personal motivations of blood scientists influenced their professional research, ultimately demonstrating how conceptually indeterminate and politically volatile the science of race was under the Nazi regime. Contrary to sustained efforts, the search for the 'Aryan' blood did not materialize into the racial utopia that the Nazi officials had dreamed. Moreover, the monograph also convincingly demonstrates how ambiguous the relationship between eugenics, seroanthropology and anti-Semitism was in Germany, not least because proeminent German eugenicists and race scientists were Jewish or of Jewish origin. Boaz provides us with an enriched picture of the myriad ways in which these scientists maneuvered within an increasing anti-Semitic Weltanschauung.
It has only recently been appreciated that the immune and skeletal systems have major interactions. It is now well documented that osteoclasts, which are important cellular mediators of skeletal homeostasis, are derived from hematopoietic precursors that also give rise to immune cells. In addition, numerous cytokines that were first shown to regulate immune cell function have also been demonstrated to regulate bone cells and influence skeletal health. Conversely, products of bone cells appear critical for the engraftment of marrow in bone, the normal development of the hematopoietic and immune systems and provide niche for long-term memory B and T cells. In the past scientists involved in immune and bone cell investigations have rarely interacted in a significant way as these disciplines have developed independently and, for the most part, remain separate. The conference will bring together leading international scientists from both fields to interact so that new collaboration can develop and more rapid progress in understanding the relationships between these fields can be achieved. Short talks will be selected from abstracts from the international community. This conference will have a format to provide an environment of maximum interaction and interchange through lectures, posters, and open discussion.
The AIDS threat has mobilized an unprecedented research effort to understand and control the disease. We have discovered its agent, HIV, the human immunodeficiency virus. Every day we know more about this complex retrovirus and how it works, but we still lack an effective defense strategy. This book will give the nonspecialist an AIDS overview and a vantage point from which to observe and support the continuing struggle with HIV. It also will urge that we look beyond this deadly virus. As we seek vaccines and therapies to stop its fatal course, we must understand that the real cause of AIDS is not HIV. It is the environmental context that allowed the virus to escape its natural host and enter the human population at this particular time in history. The question is why, after millenia of contact between African monkeys and humans, has SIV (Simian immunodeficiency virus) only now entered the human population in plague proportions? Is its introduction a purely random and natural disaster, or is it somehow the result of human social and cultural evolution? This book explains how human encroachment on the African monkey habitat set up conditions that made it possible and almost likely that the virus would successfully jump to a new host, with the consequences that we now see as the world wide AIDS epidemic. It presents the full history of the various subtypes of the virus, and the epidemics they cause, and assembles the future threats in every region of the world. The book argues that facing our responsibility for the AIDS outbreak holds the key to reversing the damage. If we study our actions and this lethal natural reaction, we can find ways to halt the AIDS and prevent similar plagues that could erupt in the future.
The behavior of lymphocytes in the immune system depends on
encounters with antigens. These bind to immunoreceptors on the
surface of T-cells and B-cells, activating a variety of signal
transduction pathways that control cell survival, proliferation,
differentiation, and effector functions.
A Primer of Neuroimmunological Disease is a significant new resource for anyone interested in conditions such as multiple sclerosis(MS), myasthenia gravis, and neurological infections. It is a practical and balanced guide to the diagnosis and treatment of neuroimmunological disease. A Primer of Neuroimmunological Disease distinguishes itself by providing a range of features not generally included in texts on neuroimmunology. These include broad presentation of information in the form of figures and tables; strong cohesion among topics by focusing on a few prototypic neuroimmunological diseases, which serve as a foundation from which to explore other neuroimmunological diseases; a single author perspective, with references across chapters; and a focus on the overlap between neuroimmunological and neuroinfectious diseases. Neurologists, immunologists, infectious disease specialists, neuroscientists and others interested in neuroimmunological diseases such as MS will find A Primer of Neuroimmunological to be a state-of-the-art resource.
Understanding Immunology is a well-established introduction to this complex subject for readers with no previous exposure. It is aimed primarily at undergraduates in biological sciences, biomedical sciences and medicine. The selection and order of topic coverage is designed to instruct effectively, and a variety of boxed examples add depth and historical context for those readers wanting to go beyond the essentials.
This volume covers methods for determination of autoantibodies in rheumatic connective tissue diseases and organ-specific diseases. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and cutting-edge, Autoantibodies: Methods and Protocols aims to be helpful for all persons working with research and development of autoimmune laboratory diagnostics and for clinicians using autoantibody tests in daily work with patients.
System Biology encompasses the knowledge from diverse fields such as Molecular Biology, Immunology, Genetics, Computational Biology, Mathematical Biology, etc. not only to address key questions that are not answerable by individual fields alone, but also to help in our understanding of the complexities of biological systems. Whole genome expression studies have provided us the means of studying the expression of thousands of genes under a particular condition and this technique had been widely used to find out the role of key macromolecules that are involved in biological signaling pathways. However, making sense of the underlying complexity is only possible if we interconnect various signaling pathways into human and computer readable network maps. These maps can then be used to classify and study individual components involved in a particular phenomenon. Apart from transcriptomics, several individual gene studies have resulted in adding to our knowledge of key components that are involved in a signaling pathway. It therefore becomes imperative to take into account of these studies also, while constructing our network maps to highlight the interconnectedness of the entire signaling pathways and the role of that particular individual protein in the pathway. This collection of articles will contain a collection of pioneering work done by scientists working in regulatory signaling networks and the use of large scale gene expression and omics data. The distinctive features of this book would be: Act a single source of information to understand the various components of different signaling network (roadmap of biochemical pathways, the nature of a molecule of interest in a particular pathway, etc.), Serve as a platform to highlight the key findings in this highly volatile and evolving field, and Provide answers to various techniques both related to microarray and cell signaling to the readers.
The 8th volume in the Proteases in Biology and Disease series focuses on the role of proteases in virus function and their potential as anti-viral targets. Viral infections are still difficult to threat and some remained life-threatening diseases in spite of antiviral drug research over decades. Proteases are still regarded as an Achilles heel of the pathogens and, thus, protease inhibitors may help to handle the known and the emerging viral threads. The book discusses viral proteases of the most important pathogenic viruses, responsible for severe diseases: AIDS, SARS, Hepatitis, Cytomegalovirus, T-cell lymphotropic virus, Picornavirus. This book focuses specifically on the viral proteases, crucial prerequisites for viral entry into cells and viral replication. Viral proteases represent an important pharmaceutical target. The current stage of protease inhibitor development and therapy are summarised and discussed by experts in the field. This volume represents a timely and valuable continuation of the Proteases in Biology and Disease series. The reader will learn the potential for proteases as targets for effective anti-virals. This book will be a valuable source of information on viral proteases and provoke further research in this important field."
This volume explains why newly emerging infections, stealth viral diseases, chronic fatigue, and immune deficiency illnesses are among the most important health problems today. Dr Williams presents theories on immunity, describing how the immune system defends against viruses, and discussing why our immune systems are breaking down. He offers a comprehensive ten-step plan for enhancing immunity and treating viral conditions.
In the 11 years since this atlas first published, the immunology field has experienced an exponential increase in information. Besides the unprecedented advances in knowledge of cell receptors and signal transduction pathways, an avalanche of new information has been gleaned from contemporary research concerning cytokines and chemokines, with special reference to their structure and function. Visually Enhances Definitions in the Language of
Immunology Completely revised and expanded, this third edition features:
Written in a highly readable, two-column format, this complete reference covers a wide array of subjects, with content ranging from photographs of field pioneers to illustrations of molecular structures of recently characterized cell receptors, chemokines, and cytokines. The atlas also addresses the major histocompatability complex molecules, immunoglobulins, hematopoietic cells in leukemia, and molecules of related interest to immunologists. You won t find another publication anywhere that matches the breadth or detail of illustrated immunological concepts."
This book includes these topics: A Key Regulator of Postnatal Skeletal Remodeling; Ectodomain Shedding of Receptor Activator of NF-KB Ligand; The Negative Role Of Ids In Osteoclastogenesis; Functional Genetic and Genomic Analysis of Modeled Arthritis; Dexamethsone Suppresses Bone Formation via the Osteoclast; Immunologic Regulation Of Bone Development; Pth Regulates The Hematopoietic Stem Cell Niche In Bone; Regulation Of Hematopoietic Stem Cells In The Osteoblastic Niche; The Chemokine Cxcl12; and Regulation Of Hsc; and Lymphocyte Development In The Bone Marrow Niche. It also includes these topics: Osteoclast Precursor Cells; Interaction with estrogen receptors as treatment of arthritis and osteoporosis; Novel Signaling Pathways And Therapeutic Targets In Osteoclasts; The Enigmatic Function of TREM-2 in Osteoclastogenesis; Role of cell-matrix interactions in osteoclast differentiation; Positive and negative roles of IL-6, STAT3 and SOCS3 in inflammatory arthritis; Control of Osteoclast activity and bone loss by IKK subunits: new targets for therapy; Targeting Osteoporosis And Rheumatoid Arthritis By Active Vaccination Against Rankl; and RANKL Inhibition: From Mice to Men (and Women).
Selected as a Doody's Core Title for 2022! Defining the field of immunology for 40 years, Paul's Fundamental Immunology continues to provide detailed, authoritative, up-to-date information that uniquely bridges the gap between basic immunology and the disease process. The fully revised 8th edition maintains the excellence established by Dr. William E. Paul, who passed away in 2015, and is now under new editorial leadership of Drs. Martin F. Flajnik, Nevil J. Singh, and Steven M. Holland. It's an ideal reference and gold standard text for graduate students, post-doctoral fellows, basic and clinical immunologists, microbiologists and infectious disease physicians, and any physician treating diseases in which immunologic mechanisms play a role. Reflects the latest advances in the field, including current insights on immune system function, both basic and translational. Contains 50 chapters written by leaders in all subfields of immunology. Provides extensive coverage of the molecular biology that explains the dynamics underlying immune disorders and their treatment. Includes 10 entirely new chapters covering invertebrate and plant immunity, eosinophils, innate lymphoid cells, gamma/delta T cells, NKT and MAIT cells, immunometabolism, maternal-fetal immunology and more. Contains abundant full-color illustrations and tables that provide essential information at a glance. Features annual updates from the authors to the VST version, keeping you current with changes in this dynamic field from the experts. Enrich Your eBook Reading Experience Read directly on your preferred device(s), such as computer, tablet, or smartphone. Easily convert to audiobook, powering your content with natural language text-to-speech.
When the world stopped, all hopes rested on finding a vaccine. An unlikely team answered the call. Before Covid-19 was even given its name, a select group of scientists in Germany, assembled by married couple and decades-long research partners Uğur Şahin and Özlem Türeci, began building 20 potential vaccines. As the deadly disease spread from country to country, what followed was a desperate race against time to conduct rigorous tests and clinical trials, whilst navigating political interference and seeking the support of the pharmaceutical industry. Shedding a light on the science behind the breakthrough, The Vaccine tells the story of the trailblazers who led the fightback against Covid-19, whose discoveries could now help the world tackle cancer, along with many other pervasive diseases. It draws back the curtain on one of the most important medical achievements of our age, containing contributions from the fascinating couple themselves, as well as more than 60 scientists, politicians, public health officials, and BioNTech staff. More suspenseful than a novel, this is a real-life story of an extraordinary race against time to save the world.
This volume provides methods to analyze the meningococcus and its interactions with biologically relevant host cells and sites, to interrogate the population structure and biology of the meningococcus that defines its capacity to cause disease, and to aid in vaccine development and surveillance. Many of these methods are applicable to the close relative, Neisseria gonorrhoeae, and several of the methods described can also be used in investigating host-pathogen interactions for a range of other organisms. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Neisseria meningitidis: Methods and Protocols will allow for the use of these methods by more laboratories and foster collaboration and consistency in investigations of this enigmatic and dangerous pathogen.
This book gives a comprehensive overview to all aspects of global molecular vaccine research. It introduces concepts of vaccine immunology and molecular vaccine development for viral, bacterial, parasitic and fungal infections. Furthermore, the broad field of research and development in molecular cancer vaccines is discussed in detail. This book is a must have for scientists and clinicians interested in new developments in molecular vaccine research and application in infections and cancer.
Analysis by In Situ Hybridization of Cytokine mRNAS Expression in Thymic Nurse Cells.- Genetic Expression of the C-CBL Proto-Oncogene in Human Thymocytes.- Production and Selection of B Lymphocytes in Bone Marrow: Lymphostromal Interactions and Apoptosis in Normal, Mutant and Transgenic Mice.- Thymic Neuroendocrine Self Peptides and T Cell Selection.- Human Fetal Liver Cells Differentiate into Thymocytes in Chimeric Mouse Fetal Thymus Organ Culture.- Towards Identification of Memory B Cells in Human Tonsils.- Prolonged IL-4 Treatment Decreases the TNP-Specific Memory Formation for IgG1.- Selection of Anti-Arsonate Idiotype (CRIA) in A/J Mice by the Immune Network.- The Life History and Functional Roles of Accessory Cells.- The Role of Macrophages in Regeneration of Splenic Tissue after Autologous Transplantation in Rat.- In Vivo Antigen Presentation Capacity of Dendritic Cells from Oral Mucosa and Skin Draining Lymph Nodes.- Liposome Mediated Modulation of Macrophage Functions.- In Vivo gp39-CD40 Interactions Occur in the Non-Follicular Compartments of the Spleen and Are Essential for Thymus Dependent Antibody Responses and Germinal Center Formation.- The Role of Dendritic Cells in the Uptake and Presentation of Oral Antigens.- Blockage of Thymic Medullary Epithelial Cell Activation: In Vivo Consequences.- Half-Lives of Antigen/MHC Class II Complexes Differ between Distinct Organ Microenvironments.- Regulation of Neural and Peripheral Cytokine Production by Benzodiazepines and Endogenous Anxiogenic Peptides.- Could ACTH be of Prime Importance in Rapidly Altering the Thymocyte Composition in the Thymus?.- Adrenergic and Cholinergic Regulation of Apoptosis and Differentiation of Thymic Lymphocytes.- Autoimmune lpr and gld Mice: Models of Abnormal Adhesion Molecule Regulation and Defective Lymphocyte Traffic.- Vascular Addressin Expression in Peyer's Patches: An in Vivo Study of Site-Associated Regulation.- Domain 5 of the Intercellular Adhesion Molecule-1 (ICAM-1) Is Involved in Adhesion of B-Cells and Follicular Dendritic Cells.- Modifications of the Expression of Homing and Adhesion Molecules in Infiltrated Islets of Langerhans in Nod Mice.- Characterization of Giant Perivascular Spaces in the Thymus of the Nonobese Diabetic Mouse.- Adhesion Molecule PECAM-1/CD31 Is Expressed on Defined Subsets of Murine LAK Cells.- Intrathymic Gap Junction-Mediated Communication.- Complement and Antibody Enhance Binding and Uptake of HIV-1 by Bone Marrow Cells.- Follicular Dendritic Cells (FDC) Are Not Productively Infected with HIV-1 in Vivo.- Lymph Node Pathology in Experimental FIV Infection.- Lymphocyte Lifespan in Murine Retrovirus-Induced Immunodeficiency.- Analysis of HIV Infections in Human Macrophage-Like Cell Lines.- The Pivotal Role of the Immunoglobulin Receptor of Tumor Cells from B Cell Lymphomas of Mucosa Associated Lymphoid Tissue (MALT).- TNF?- Is Involved in the Mechanism of Murine Thymic Lymphoma Prevention by Bone Marrow Grafting.- Analysis of Germinal Centres in the Immune Response to Oxazolone.- Cytokine Responsiveness of Germinal Center B Cells.- The Differences in Survival and Phenotype between Centroblasts and Centrocytes.- In Vivo Localisation Patterns and Cell-Cell Interactions of Cytokine Producing T-Cells and Specific Antibody Forming B-Cells.- DHEAS Enhances Germinal Center Responses in Old Mice.- Cellular Origin of Follicular Dendritic Cells.- Germinal Centers Develop at Predilicted Sites in the Chicken Spleen.- Expression and Function of DRC-1 Antigen.- The Appendix Functions as a Mammalian Bursal Equivalent in the Developing Rabbit.- Development of Components of the Mucosal Immune System in SCID Recipient Mice.- Many Newly Formed T Lymphocytes Leave the Small Intestinal Mucosa via Lymphatics.- Analysis of IgA-Producing Hybridomas Derived from Peritoneal Bl Cells.- Modulation of the Neonatal IgA Response to Enteric Antigens by Maternal Antibody.- Antibody-Forming Cells (AFCs) in the Lung Lymphoid Tissue afte...
Glycosylation is a common and extremely important modification in biological molecules, particularly of proteins. "HIV Glycans in Infection and Immunity"provides an overview of the roles of glycans in the transmission/infection, antigenicity, and immunogenicity of HIV and the HIV envelope glycoprotein. It explores recent advances in the understanding of the impact of HIV glycans in infection and their promise for immunological and therapeutic intervention. Novel collaborations between glycobiologists and immunologists in recent years have led to key advances in the understanding of HIV glycans. These cross-disciplinary endeavors, their achievements and their impact on the field are all addressed, herein."
Silicone Gels as Adjuvants: Effects on Humoral and Cellmediated Immune Responses; J.O. Naim, C.J. van Oss The Effect of Molecular Weight and Gel Preparation on Humoral Adjuvancy of Silicone Oils and Silicone Gels; J.O. Naim, C.J. van Oss Glucans as Immunological Adjuvants; N. Mohagheghpour, et al. Copolymer Adjuvants; R.N. Brey Regulation of Il4 and Il5 Secretion by Histamine and PGE2; M.M. Khan Immunoglobulin Isotype Modulation after Administration of Il12; V. Van Cleave, et al. Substance P Mediated Stimulation of Cytokine Levels in Cultured Murine Bone Marrow Stromal Cells; J.M. Manske, et al. Malaria Transmissionblocking Immunity: Identification of Epitopes and Evaluation of Immunogenicity; N. Kumar, et al. Experimental Feline Lyme Borreliosis As a Model for Testing Borrelia burgdorferi Vaccines; M.D. Gibson, et al. Liposoma Vaccines; S. Green, et al. Protection Strategies against Botulinum Toxin; L. Middlebrook Collagen Arthritis in T Cell Receptor Congenic Mice: A Unique Approach to Study the Role of T Cell Receptor Genotypes in Autoimmune Arthritis; G.H.H. Nabozny, C.S. David The Blood-Brain Barrier in Virusinduced Demyelination; C.J.R. Welsh, et al. 14 additional articles. Index.
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