Immunology at a Glance

J. H. L. Playfair, B. M. Chain

• Publisher: Wiley-Blackwell
• Year: 2012
• Print ISBN:
  9780470673034
• eBook ISBN:
  9781118447468
• Edition: 10
• Topic: Medicine
• Subtopic: Pulmonary & Thoracic Medicine

Immunology at a Glance provides a user-friendly overview of the body's defence mechanisms. Ideal from day one of a medical, biomedical or life science course, the text begins with a basic overview of both adaptive and innate immunity, before progressing to applied immunological concepts, which look at what happens when things go wrong, and how, in clinical medicine, each body system can be affected by immunity.

Each double-page spread corresponds to a typical lecture and diagrammatically summarises core concepts in immunology, through accessible schematic diagrams on left-hand pages, with key points concisely summarised on the right-hand page. There are also self-assessment essay questions so you can test your knowledge.

New for this 10th edition:

• Thoroughly updated and reorganised chapters offer greater clarity and easier understanding for those new to the subject
• New chapters on cytokine receptors and 'Immunology in the Laboratory'
• A completely re-written section on autoimmunity
• A brand new companion website featuring self-assessment questions and PowerPoint slides of images from the book, ideal for teaching and revision at www.ataglanceseries.com/immunology

Immunology at a Glance is the ideal companion for anyone about to start a new course in immunology and will appeal to medical and biomedical science students. Perfect for exam preparation, it provides the concepts and frameworks you need to succeed in your exam.

1
The Scope of Immunology

Of the four major causes of death – injury, infection, degenerative disease and cancer – only the first two regularly kill their victims before child-bearing age, which means that they are a potential source of lost genes. Therefore any mechanism that reduces their effects has tremendous survival value, and we see this in the processes of, respectively, healing and immunity.

Immunity is concerned with the recognition and disposal of foreign or ‘non-self’ material that enters the body (represented by red arrows in the figure), usually in the form of life-threatening infectious microorganisms but sometimes, unfortunately, in the shape of a life-saving kidney graft. Resistance to infection may be ‘innate’ (i.e. inborn and unchanging) or ‘acquired’ as the result of an adaptive immune response (centre).

Immunology is the study of the organs, cells and molecules responsible for this recognition and disposal (the ‘immune system’), of how they respond and interact, of the consequences – desirable (top) or otherwise (bottom) – of their activity, and of the ways in which they can be advantageously increased or reduced.

By far the most important type of foreign material that needs to be recognized and disposed of is the microorganisms capable of causing infectious disease and, strictly speaking, immunity begins at the point when they enter the body. But it must be remembered that the first line of defence is to keep them out, and a variety of external defences have evolved for this purpose. Whether these are part of the immune system is a purely semantic question, but an immunologist is certainly expected to know about them.

Non-Self 

A widely used term in immunology, covering everything that is detectably different from an animal’s own constituents. Infectious microorganisms, together with cells, organs or other materials from another animal, are the most important non-self substances from an immunological viewpoint, but drugs and even normal foods, which are, of course, non-self too, can sometimes give rise to immunity. Detection of non-self material is carried out by a range of receptor molecules (see Figs 5, 10–14).

Infection 

Parasitic viruses, bacteria, protozoa, worms or fungi that attempt to gain access to the body or its surfaces are probably the chief raison d’être of the immune system. Higher animals whose immune system is damaged or deficient frequently succumb to infections that normal animals overcome.

External Defences 

The presence of intact skin on the outside and mucous membranes lining the hollow viscera is in itself a powerful barrier against entry of potentially infectious organisms. In addition, there are numerous antimicrobial (mainly antibacterial) secretions in the skin and mucous surfaces; these include lysozyme (also found in tears), lactoferrin, defensins and peroxidases. More specialized defences include the extreme acidity of the stomach (about pH 2), the mucus and upwardly beating cilia of the bronchial tree, and specialized surfactant proteins that recognize and clump bacteria that reach the lung alveoli. Successful microorganisms usually have cunning ways of breaching or evading these defences.

Innate Resistance 

Organisms that enter the body (shown in the figure as dots or rods) are often eliminated within minutes or hours by inborn, ever-present mechanisms, while others (the rods in the figure) can avoid this and survive, and may cause disease unless they are dealt with by adaptive immunity (see below). These mechanisms have evolved to dispose of pathogens (e.g. bacteria, viruses) that if unchecked can cause disease. Harmless microorganisms are usually ignored by the innate immune system. Innate immunity also has a vital role in initiating the adaptive immune response.

Adaptive Immune Response 

The development or augmentation of defence mechanisms in response to a particular (‘specific’) stimulus, e.g. an infectious organism. It can result in elimination of the microorganism and recovery from disease, and often leaves the host with specific memory, enabling it to respond more effectively on reinfection with the same microorganism, a condition called acquired resistance. Because the process by which the body puts together the receptors of the adaptive immune system is random (see Fig. 10), adaptive immunity sometimes responds to harmless foreign material such as the relatively inoffensive pollens, etc., or even to ‘self’ tissues leading to autoimmunity.

Vaccination 

A method of stimulating the adaptive immune response and generating memory and acquired resistance without suffering the full effects of the disease. The name comes from vaccinia, or cowpox, used by Jenner to protect against smallpox.

Grafting 

Cells or organs from another individual usually survive innate resistance mechanisms but are attacked by the adaptive immune response, leading to rejection.

Autoimmunity 

The body’s own (‘self’) cells and molecules do not normally stimulate its adaptive immune responses because of a variety of special mechanisms that ensure a state of self-tolerance, but in certain circumstances they do stimulate a response and the body’s own structures are attacked as if they were foreign, a condition called autoimmunity or autoimmune disease.

Hypersensitivity 

Sometimes the result of specific memory is that re-exposure to the same stimulus, as well as or instead of eliminating the stimulus, has unpleasant or damaging effects on the body’s own tissues. This is called hypersensitivity; examples are allergies such as hay fever and some forms of kidney disease.

Immunosuppression 

Autoimmunity, hypersensitivity and, above all, graft rejection sometimes necessitate the suppression of adaptive immune responses by drugs or other means.

2
Innate and Adaptive Immune Mechanisms

Just as resistance to disease can be innate (inborn) or acquired, the mechanisms mediating it can be correspondingly divided into innate (left) and adaptive (right), each composed of both cellular (lower half) and humoral elements (i.e. free in serum or body fluids; upper half). Adaptive mechanisms, more recently evolved, perform many of their functions by interacting with the older innate ones.

Innate immunity is activated when cells use specialized sets of receptors (see Fig. 5) to recognize different types of microorganisms (bacteria, viruses, etc.) that have managed to penetrate the hos...

Table of contents

• Cover
• Table of Contents
• Companion Website
• Title
• Copyright
• Preface
• Acknowledgements
• Note on the Tenth Edition
• How to Use This Book
• Further Reading
• List of Abbreviations
• 1 The Scope of Immunology
• 2 Innate and Adaptive Immune Mechanisms
• 3 Recognition and Receptors: The Keys to Immunity
• 4 Cells Involved in Immunity: The Haemopoietic System
• 5 Receptors of the Innate Immune System
• 6 Complement
• 7 Acute Inflammation
• 8 Phagocytic Cells and the Reticuloendothelial System
• 9 Phagocytosis
• 10 Evolution of Recognition Molecules: The Immunoglobulin Superfamily
• 11 The Major Histocompatibility Complex
• 12 The T-Cell Receptor
• 13 Antibody Diversification and Synthesis
• 14 Antibody Structure and Function
• 15 Lymphocytes
• 16 Primary Lymphoid Organs and Lymphopoiesis
• 17 Secondary Lymphoid Organs and Lymphocyte Traffic
• 18 Antigen processing and presentation
• 19 The Antibody Response
• 20 Antigen – Antibody Interaction and Immune Complexes
• 21 Cell-Mediated Immune Responses
• 22 Tolerance
• 23 Cell Communication and Cytokines
• 24 The Cytokine Network
• 25 Immunity, Hormones and the Brain
• 26 Antimicrobial Immunity: a General Scheme
• 27 Immunity to Viruses
• 28 HIV and AIDS
• 29 Immunity to Bacteria
• 30 Immunity to Fungi and Ectoparasites
• 31 Immunity to Protozoa
• 32 Immunity to Worms
• 33 Immunodeficiency
• 34 Harmful Immunity: a General Scheme
• 35 Allergy and Anaphylaxis
• 36 Immune Complexes, Complement and Disease
• 37 Chronic and cell-mediated inflammation
• 38 Autoimmune Disease
• 39 Transplant Rejection
• 40 Immunosuppression
• 41 Immunostimulation and Vaccination
• 42 Cancer Immunology
• 43 Immunity and Clinical Medicine
• 44 Investigating Immunity
• 45 Immunology in the Laboratory
• 46 Out of the Past: Evolution of Immune Mechanisms
• 47 Into the future: immunology in the age of genomics
• Self-Assessment Questions
• Answers
• Appendix I: Comparative Sizes
• Appendix II: Landmarks in the History of Immunology
• Appendix III: CD Classification
• Index
• End User License Agreement