- •6. Genetic Resistance to Infection
- •2. Primary Lymphoid Organs
- •3. Lymphatic System
- •4. Secondary Lymphoid Organs
- •5. Cutaneous-Associated Lymphoid Tissue
- •1. The Adaptive Immune System Requires Cooperation Between Lymphocytes and Antigen-Presenting Cells
- •2. Humoral Immunity But Not Cellular Immunity Is Transferred with Antibody
- •3. Antigen Is Recognized Differently by b and t Lymphocytes
- •4. B and t Lymphocytes Utilize Similar Mechanisms To Generate Diversity in Antigen Receptors
- •5. The Major Histocompatibility Molecules Bind Antigenic Peptides
- •6. Complex Antigens Are Degraded (Processed) and Displayed (Presented) with mhc Molecules on the Cell Surface
- •7. Antigen Selection of Lymphocytes Causes Clonal Expansion
- •8. The Innate and Adaptive Immune Systems Collaborate, Increasing the Efficiency of Immune Responsiveness
- •1. Immunogenicity Versus Antigenicity
- •2. Factors That Influence Immunogenicity
- •3. The Nature of the Immunogen Contributes to Immunogenicity
- •4. The Biological System Contributes to Immunogenicity
- •5. Epitopes
- •5.1 Properties of b-Cell Epitopes Are Determined by the Nature of the Antigen-Binding Site
- •5.2 Antigen-Derived Peptides Are the Key Elements of t-Cell Epitopes
- •6. Haptens and the Study of Antigenicity
- •Antibody-Antigen Interactions and the Function of the Fab
- •Figure 3 Summary of antibody functions.
- •Functions of the Crystallizable Fragment
- •Accessory Molecules on Immunoglobulins
- •The Classes of Immunoglobulins
- •Characteristics of the Immunoglobulin (Ig) Classes
- •Monoclonal Antibodies: Useful Products from Cancer Cells
- •Figure 4 Summary of the technique for producing monoclonal antibodies by hybridizing myeloma tumor cells with normal plasma cells.
- •Some Important Cytokines
- •Characteristics of Interferon
- •Antiviral Interferon
- •Figure 3. Steps in recombinant dna, gene cloning, and product retrieval.
8. The Innate and Adaptive Immune Systems Collaborate, Increasing the Efficiency of Immune Responsiveness
It is important to appreciate that adaptive and innate immunity do not operate independently – they function as a highly interactive and cooperative system, producing a combined response more effective than either branch could produce by itself. Certain immune components play important roles in both types of immunity.
An example of cooperation is seen in the encounter between macrophages and microbes. Interactions between receptors on macrophages and microbial components generate soluble proteins that stimulate and direct adaptive immune responses, facilitating the participation of the adaptive immune system in the elimination of the pathogen. Stimulated macrophages also secrete cytokines that can direct adaptive immune responses against particular intracellular pathogens.
Just as important, the adaptive immune system produces signals and components that stimulate and increase the effectiveness of innate responses. Some T cells, when they encounter appropriately presented antigen, synthesize and secrete cytokines that increase the ability of macrophages to kill the microbes they have ingested. Also, antibodies produced against an invader bind to the pathogen, marking it as a target for attack by complement and serving as a potent activator of the attack.
A major difference between adaptive and innate immunity is the rapidity of the innate immune response, which utilizes a pre-existing but limited repertoire of responding components. Adaptive immunity compensates for its slower onset by its ability to recognize a much wider repertoire of foreign substances, and also by its ability to improve during a response, whereas innate immunity remains constant. It may also be noted that secondary adaptive responses are considerably faster than primary responses. Principle characteristics of the innate and adaptive immune systems are compared in Table 1.With overlapping roles, the two systems together form a highly effective barrier to infection.
Table 1
Comparison of adaptive and innate immunity
Lecture 1.5 Antigens, their structure, properties
Antigens
Plan:
Introduction
1. Immunogenicity Versus Antigenicity
2. Factors That Influence Immunogenicity
3. The Nature of the Immunogen Contributes to Immunogenicity
4. The Biological System Contributes to Immunogenicity
5. Epitopes
5.1 Properties of B-Cell Epitopes Are Determined by the Nature of the Antigen-Binding Site
5.2 Antigen-Derived Peptides Are the Key Elements of T-Cell Epitopes
6. Haptens and the Study of Antigenicity
Introduction
Substances that can be recognized by the immunoglobulin receptor of B cells, or by the T cell receptor when complexed with MHC, are called antigens. The molecular properties of antigens and the way in which these properties ultimately contribute to immune activation are central to our understanding of the immune system. This lecture describes some of the molecular features of antigens recognized by B or T cells. The lecture also explores the contribution made to immunogenicity by the biological system of the host; ultimately the biological system determines whether a molecule that combines with a B or T cell’s antigen-binding receptor can then induce an immune response. Fundamental differences in the way B and T lymphocytes recognize antigen determine which molecular features of an antigen are recognized by each branch of the immune system.
