BIOL 2228_Imunity_chapt22revised
Chapter 22 Immunity: The Body's Defenses
22.1 Overview of Diseases Caused by Infectious Agents
Learning Objectives:
Compare and contrast the five major classes of infectious agents.
Describe prions, and name a disease they cause.
Overview of Infectious Agents
Infectious agents can damage or kill a host.
Pathogenic agents = disease-causing.
Five major categories:
Bacteria
Viruses
Fungi
Protozoans
Multicellular parasites
22.1.1 Bacteria
Characteristics:
Single-celled prokaryotes (1 to 2 µm).
Variants: cocci (spherical), bacilli (rod-like), spirilla (coiled).
Most bacteria are harmless; some are virulent.
Examples:
Clostridium tetani (tetanus)
Streptococcal bacteria (strep throat)
22.1.2 Viruses
Characteristics:
Non-cellular; much smaller (one-hundredth of a micrometer).
Obligate intracellular parasites; must enter host cells to reproduce.
Cause cell death directly or via immune response.
Examples:
Common cold, Ebola, chickenpox
22.1.3 Fungi
Characteristics:
Eukaryotic cells with both membrane and cell wall.
Includes molds, yeasts.
Can cause superficial infections (e.g., ringworm) or systemic infections (e.g., histoplasmosis).
22.1.4 Protozoans
Characteristics:
Eukaryotic, lack cell walls.
Can be intracellular or extracellular parasites.
Example:
Malaria, trichomoniasis
22.1.5 Multicellular Parasites
Characteristics:
Macroscopic organisms that take nourishment from their host.
Example:
Tapeworms
22.1.6 Prions
Characteristics:
Infectious proteins, neither cells nor viruses.
Cause diseases in nervous tissue.
Example:
Variant Creutzfeldt-Jakob disease (mad cow disease).
22.2 Overview of the Immune System
Learning Objectives:
List leukocytes of the immune system and their locations.
Define cytokines and their similarities to hormones.
List general categories of cytokines.
Compare primary features of innate and adaptive immunity.
22.2a Immune Cells and Their Locations
Leukocytes (white blood cells):
Formed in red bone marrow.
Types:
Granulocytes (neutrophils, eosinophils, basophils)
Monocytes (become macrophages in tissues)
Lymphocytes (B-lymphocytes, T-lymphocytes, NK cells)
22.2b Cytokines
Cytokines: Small proteins that regulate immune activity.
Effects:
Signal cells, control immune cell development, regulate inflammatory responses, destroy cells.
Types:
Autocrine, paracrine, endocrine.
22.2c Comparison of Innate and Adaptive Immunity
Innate Immunity:
Present at birth, nonspecific, no prior exposure needed.
Features include physical (skin) and chemical barriers, cellular defenses.
Adaptive Immunity:
Acquired/specific; requires exposure to specific antigens.
Involves T- and B-lymphocytes; develops over several days.
22.3 Innate Immunity
Learning Objectives:
Describe barriers to entry of harmful agents.
Describe cells involved in nonspecific defenses (innate immunity).
Explain functions of interferons.
Define the complement system and how it is activated.
Describe how the complement system participates in innate immunity.
22.3a First Line: Preventing Entry
Skin and Mucous Membranes:
Skin releases antimicrobial substances (e.g., dermicidin).
Mucous membranes produce mucus and antimicrobial substances (e.g., defensins, IgA).
22.3b Second Line: Nonspecific Internal Defenses
Phagocytic Cells:
Include neutrophils, macrophages, dendritic cells; engulf unwanted substances.
Chemicals / Cytokines:
Released by cells like basophils and mast cells; promote inflammation and attract immune cells.
NK Cells:
Destroy unhealthy cells by releasing perforin and granzymes, inducing apoptosis.
22.4 Adaptive Immunity: An Introduction
Learning Objectives:
Describe features of antigens and antigenic determinants.
Explain immunogenicity and its affecting attributes.
Discuss how haptens stimulate immune responses.
Describe receptors of T-lymphocytes and B-lymphocytes.
22.4a Antigens
Definition:
Substances that bind T-lymphocytes or antibodies; usually proteins or large polysaccharides.
Types:
Foreign antigens (non-self) vs. self-antigens.
Immune system usually recognizes self-antigens but can react in autoimmune disorders.
22.5 Formation and Selection of T-Lymphocytes
Learning Objectives:
Explain T-lymphocyte maturation.
Compare and contrast positive and negative selection in thymus.
22.5a Formation of T-Lymphocytes
Origin in red bone marrow; they migrate to thymus as pre-T-lymphocytes for maturation.
22.5b Selection and Differentiation of T-Lymphocytes
Thymic Selection:
Positive selection: survival of those that can bind MHC molecules.
Negative selection: removal of cells that bind self-antigens.
22.6 Activation and Clonal Selection of Lymphocytes
Learning Objectives:
Describe activation mechanisms for T-lymphocytes and B-lymphocytes.
Explain lymphocyte recirculation and its function.
22.6a Activation of T-Lymphocytes
Helper T-Lymphocytes:
First signal: direct contact with MHC on APC.
Second signal: cytokine release and cell proliferation.
Cytotoxic T-Lymphocytes:
Activated similarly, but target infected cells directly.
22.6b Activation of B-Lymphocytes
Activation Steps:
Antigen binds to BCR and is presented to helper T-cell.
Helper T-cell releases cytokines to stimulate B-cell.
22.7 Effector Response at Infection Site
Learning Objectives:
Describe functions of T-lymphocytes and plasma cells during effector response.
22.7a Effector Response of T-Lymphocytes
Helper T-cells: regulate immune responses and activate other immune cells.
Cytotoxic T-cells: destroy unhealthy cells through apoptosis.
22.7b Effector Response of B-Lymphocytes
Plasma cells: produce and release antibodies, forming high antibody titers against specific antigens.
22.8 Immunoglobulins
Structure: Y-shaped proteins composed of heavy and light chains, with variable and constant regions.
Functions of Antibodies:
Neutralization, agglutination, precipitation, complement fixation, opsonization, activation of NK cells.
22.9 Immunologic Memory and Immunity
Learning Objectives:
Define immunologic memory and explain its significance.
Discuss differences between primary and secondary responses.
22.9a Immunologic Memory
Results in a long-lived army of memory lymphocytes; secondary responses are more rapid and effective.
22.9b Active and Passive Immunity
Active Immunity: Developed through exposure to pathogens; produces memory cells.
Passive Immunity: Transferred antibodies without memory cells being formed.